{"jobs":[{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4675146005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4425706005,"location":{"name":"Remote, United States"},"metadata":null,"id":4675146005,"updated_at":"2026-03-25T17:39:32-04:00","requisition_id":"433","title":"Associate Director, Clinical Supply","company_name":"4D Molecular Therapeutics","first_published":"2026-03-20T11:37:37-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;GENERAL SUMMARY:\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Associate Director, Clinical Supply is responsible for projecting, planning, executing, and overseeing all supply chain activities related to clinical trial materials. This includes managing the procurement, production, packaging, labeling, distribution, and inventory of clinical trial materials to meet company goals within the defined timelines. This role ensures that clinical supplies, including investigational product, comparators, auxiliary IMPs, and supplies, are delivered on time, within budget, and in compliance with regulatory requirements. This role involves close collaboration with various departments, including Clinical Operations, Clinical Science, Quality Assurance, Regulatory Affairs, Manufacturing, and external vendors. Effective communication with stakeholders at all levels is required to provide regular updates on supply chain status and address any concerns.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Serve as the primary point of contact for clinical supply-related inquiries and issues.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;RESPONSIBILITIES:\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Supply Planning and Management:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement clinical supply strategies to support global clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead Phase 1 to 3 clinical trial materials planning and execution. Participate in cross-functional discussions early in the study design phase to ensure that material lead-time is properly built in for overall program timeline.\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;This includes Investigational Products (IP), diluent, comparator drugs, ancillary supplies, or any other clinical materials required and identified by each project team\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Create detailed supply plans based on trial requirements, enrollment forecasts, and study timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee material requirements for domestic and international study execution. Ensure procurement, production, packaging, labeling, and distribution of clinical trial materials are done per applicable local and international guidance\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Inventory Control and Distribution:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Manage inventory levels to ensure sufficient supply of clinical trial materials while minimizing waste.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review of clinical supply requests, placing ancillary supply orders, and communicating IP demands\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate the distribution of clinical supplies to CMO and study sites, ensuring timely delivery and adherence to protocols.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor and track shipment status, resolving any issues that arise during transit.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Vendor Management.\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Identify, select, and manage relationships with suppliers, manufacturers, and logistics providers including CMOs and CROs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan and coordinate clinical supply activities including labeling, packaging, distribution of clinical trial supplies, randomization, and drug accountability systems control.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Negotiate contracts and service agreements with vendors to ensure cost-effective and high-quality supply chain operations.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Project Management:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Participate in supply chain business process development project.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive continuous operational performance improvement efforts.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with Good Manufacturing Practices and applicable state and federal regulatory authorities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Others\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Generate and maintain various clinical supply inventory reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure process execution is conducted per internal policy and procedures\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify opportunities for process improvements and implement best practices in clinical supply chain management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform other duties as assigned.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;QUALIFICATIONS:\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Education:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in supply chain or other disciplines with equivalent industry experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Experience:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;8+ years of experience in clinical or in combination with commercial supply chain management, with at least 3 years in a senior or managerial role.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In-depth knowledge of clinical trial processes, GMP, GCP, and regulatory requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience in managing complex global supply chains for clinical trials (including Europe, APAC and South America)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience with high-complexity Phase 3 trials\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Skills:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong project management skills, with the ability to lead cross-functional teams and manage multiple priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent negotiation, communication, and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in supply chain management software and tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving abilities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work in a fast-paced, dynamic environment and adapt to changing priorities.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Travel: \u0026amp;lt;5%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Physical Requirements and Working Conditions:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Base salary compensation range: $177,000 - 205,000\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Please note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135268005,"name":"512000 - Supply Chain","child_ids":[],"parent_id":4006905005}],"offices":[{"id":4006441005,"name":"Hybrid","location":"Emeryville, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4689967005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4432894005,"location":{"name":"Remote, United States"},"metadata":null,"id":4689967005,"updated_at":"2026-05-14T21:22:08-04:00","requisition_id":"452","title":"Clinical Research Associate (Contract)","company_name":"4D Molecular Therapeutics","first_published":"2026-04-29T13:09:12-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;GENERAL SUMMARY\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT seeks a motivated and detail-oriented\u0026lt;strong\u0026gt; In-House \u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Unmasked\u0026lt;/span\u0026gt; Clinical Research Associate\u0026lt;/strong\u0026gt; (uIHCRA) to support the Company’s clinical trial activities. This position reports to the Unmasked Clinical Trial Manager, Clinical Operations, and will support the day-to-day execution of a Phase 3 clinical trial, including study start-up, conduct, and close-out activities.\u0026amp;nbsp; \u0026lt;em\u0026gt;\u0026lt;strong\u0026gt;Role requires extensive experience in unmasked clinical settings.\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The uIHCRA will serve as a key liaison between 4DMT, clinical sites, and CRO partners, with a focus on site support, monitoring oversight, regulatory compliance, and data quality. This role requires strong written and verbal communication skills, excellent organizational skills, and the ability to manage competing priorities while delivering high-quality work in a fast-paced, team-oriented environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;MAJOR DUTIES \u0026amp;amp; RESPONSIBILITIES:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Clinical Trial Operations \u0026amp;amp; Site Support\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support study execution across start-up, conduct, and close-out phases\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a primary unmasked sponsor point of contact for unmasked clinical site staff in collaboration with CRO field unmasked CRAs/monitors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Communicate directly with unmasked site staff and unmasked CRO partners to obtain updates, resolve issues, and support study timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support site initiation, ongoing site management, and site close-out activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with identification, documentation, tracking, and follow-up of site issues\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Monitoring Oversight\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support oversight of unmasked CRO monitoring activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Review unmasked monitoring visit reports and follow up on action items and unresolved findings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track monitoring deliverables and escalate issues to the Unmasked Clinical Trial Manager, Clinical Operations as appropriate\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support inspection readiness and audit activities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Tracking \u0026amp;amp; Study Oversight\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate tracking tools for assigned studies, including:\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Site start up and activation status\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Initial IP supply and Ancillary supply\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Site visit activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;IP Shipment status and delivery\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist with preparation of study status reports and metrics\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Regulatory Documentation \u0026amp;amp; TMF Management\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collect, review, and track site applicable SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure timely filing of unmasked documents in the TMF/eTMF in accordance with TMF plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform TMF quality control activities and support TMF audits and study close out\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the review of Quality Incidents and follow up activities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Study Communications \u0026amp;amp; Meetings\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support organization and coordination of internal team meetings, and other study related meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare meeting materials, take meeting minutes, and maintain action item logs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support communication of study updates to internal stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Additional Responsibilities\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Support ad hoc Clinical Operations projects as assigned\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Willingness to travel as trial needs demand (\u0026amp;lt;15% anticipated)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned, nothing in this position description restricts management’s right to assign or reassign duties and responsibilities to this position at any time\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;QUALIFICATIONS:\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Education:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;A. or B.S. degree required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Experience:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 4+ years of experience supporting clinical trials in a sponsor or CRO environment on the unmasked side\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting Phase 3 clinical trials preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ophthalmology Preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Other Qualifications/Skills:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of clinical trial operations and ICH GCP guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with TMF/eTMF systems (Veeva Vault preferred)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities and meet deadlines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills and ability to collaborate effectively with cross functional teams and external partners\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Travel: Willingness to travel as business needs demand (\u0026amp;lt;15% anticipated)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Physical Requirements and Working Conditions:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Compensation range: $61.00 TO 71.00 /HOURLY\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Please note, the compensation range and actual rate offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135261005,"name":"432000 - Clinical Operations","child_ids":[],"parent_id":4006905005}],"offices":[{"id":4002254005,"name":"Remote","location":"United States","child_ids":[4054753005,4055982005,4055983005,4050218005,4050194005,4050195005,4050196005,4050207005,4050197005,4050198005,4050199005,4053980005,4050200005,4050202005,4050205005,4050201005,4050203005,4050204005,4050206005],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4694433005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4435142005,"location":{"name":"Emeryville, California; Remote, United States"},"metadata":null,"id":4694433005,"updated_at":"2026-05-11T20:34:09-04:00","requisition_id":"456","title":"Clinical Supply Specialist (Contract)","company_name":"4D Molecular Therapeutics","first_published":"2026-05-11T20:30:36-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;GENERAL SUMMARY:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Director, Supply Chain, this role is expected to work closely within the Supply Chain team, as well as cross-functional groups such as Clinical Operations and Quality.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This is a remote or hybrid position.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;RESPONSIBILITIES: \u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Supports the development and execution of Clinical Supply strategies for all 4DMT’s Phase 1/2/3 investigational drug products and ancillaries\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and track bulk drug orders to ensure adherence to pre-defined supply and resupply timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor site inventory on a daily basis; coordinate and and track drug shipments to ensure uninterrupted supply\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports drug product inventory management and distribution in partnership with 4DMT’s clinical partners; evaluates drug utilization versus forecast considering country requirements and logistical timeline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintains study and depot-level accountability and reconciliation documentation to support regulatory compliance and study closeout\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Tracks and resolves study and depot level temperature excursions. Provide routine reporting of drug wastage due to these excursions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Archives Proof of Delivery (POD) documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain traceable documentation to support GXP activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Archives documentation on Trial Master Files as required\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;QUALIFICATIONS:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Education and Experience:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Degree in biological or life sciences, pharmacy or medicine (or international equivalent). A minimum of 3 years in the pharmaceutical industry or relevant work experience and a minimum of 1 year in Clinical Supply Chain.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiar in the daily management and operations of a Clinical Supply Chain inclusive of bulk management, distribution, and maintaining study blinds across multiple investigational products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experienced with Interactive Response Technology - IRT systems for inventory management and resupply\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of regulations relating to clinical labeling, packaging, and distribution activities; working knowledge of GMP/GCP/GLP regulations\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Skills:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Intermediate/Advanced knowledge of Microsoft Suites\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of Clinical Supply Management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent planning and organizational skills and the ability to work simultaneously on multiple projects with tight timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal and communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Positive attitude with a strong desire for continuous learning\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Hourly compensation range: $58.00 - 70.00\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135268005,"name":"512000 - Supply Chain","child_ids":[],"parent_id":4006905005}],"offices":[{"id":4002254005,"name":"Remote","location":"United States","child_ids":[4054753005,4055982005,4055983005,4050218005,4050194005,4050195005,4050196005,4050207005,4050197005,4050198005,4050199005,4053980005,4050200005,4050202005,4050205005,4050201005,4050203005,4050204005,4050206005],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4654856005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4416637005,"location":{"name":"Remote, United States"},"metadata":null,"id":4654856005,"updated_at":"2026-03-10T12:10:37-04:00","requisition_id":"408","title":"Clinical Technology Manager","company_name":"4D Molecular Therapeutics","first_published":"2026-01-30T20:34:12-05:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;h3\u0026gt;GENERAL SUMMARY:\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Clinical Technology, IT professional is the accountable owner for the strategy, delivery, and operational integrity of information systems supporting 4DMT’s Clinical Research and Development organization. This role ensures clinical systems are fit for purpose, inspection-ready, and maintained in a validated state, while advancing technology solutions that enable efficient, compliant clinical execution.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The position serves as the primary liaison between Clinical R\u0026amp;amp;D, Data Management, IT, and external vendors, driving alignment, governance, and disciplined system ownership across the full lifecycle—from design and implementation through operation and retirement.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;MAJOR DUTIES \u0026amp;amp; RESPONSIBILITIES:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Own and operate clinical systems as system owner, including access control, configuration, validation, and lifecycle management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure systems remain compliant with GxP regulations and internal SOPs, preserving data integrity and inspection readiness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead requirements definition, solution design, and implementation planning with cross-functional stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide Level-2 application support and vendor coordination for incident resolution and system enhancements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and continuously improve system documentation, including validation deliverables, SOPs, and operational records.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical Data Management to support data quality, flow, and operational needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute core system governance activities, including performance monitoring, upgrades, disaster recovery testing, access reviews, and license and vendor management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive system adoption through training, documentation, and user enablement.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support audits and regulatory inspections, including inspection responses, remediation, and CAPA closure.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to product roadmaps and release planning, balancing business value, regulatory risk, and technical feasibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and maintain collaborative relationships with core business partners.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;QUALIFICATIONS:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;8–12+ years of experience implementing and operating technology solutions supporting clinical research and development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience across the CSV lifecycle, including validation, production deployment, support, and decommissioning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of FDA and EMA regulations, including 21 CFR Part 11, Parts 210/211, EU Annex 11, CSA principles, and GDPR.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Broad technical fluency across applications, infrastructure, cloud platforms, integrations, and operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in Computer Science, Engineering, Life Sciences, or a related discipline (or equivalent experience).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;h3\u0026gt;Preferred Experience:\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Collaboration with Clinical Data Management and Biometrics teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with Medidata Rave, SAS (Grid, Viya, 9.4), Spotfire, and Veeva TMF and RIM.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience operating systems in Google Cloud environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong vendor management and service governance experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with product road mapping, KPIs, and SLAs aligned to clinical priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to low-code platforms and applied AI in clinical research.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Base salary compensation range: $110,000 - $150,000\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135248005,"name":"331000 - IT Enterprise","child_ids":[],"parent_id":4006947005}],"offices":[{"id":4050208005,"name":"4D Molecular Therapeutics HQ","location":null,"child_ids":[],"parent_id":4050193005},{"id":4006441005,"name":"Hybrid","location":"Emeryville, California, United States","child_ids":[],"parent_id":null},{"id":4002254005,"name":"Remote","location":"United States","child_ids":[4054753005,4055982005,4055983005,4050218005,4050194005,4050195005,4050196005,4050207005,4050197005,4050198005,4050199005,4053980005,4050200005,4050202005,4050205005,4050201005,4050203005,4050204005,4050206005],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4673763005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4425065005,"location":{"name":"Remote, United States"},"metadata":null,"id":4673763005,"updated_at":"2026-03-16T21:33:19-04:00","requisition_id":"421","title":"Clinical Trial Manager","company_name":"4D Molecular Therapeutics","first_published":"2026-03-16T21:33:19-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;GENERAL SUMMARY:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;The Clinical Trial Manager will support the Company\u0026#39;s clinical trial activities.\u0026amp;nbsp; This position reports to the Director of Clinical Operations.\u0026amp;nbsp; This will be responsible for management of the day to day operations of one or more phase 1-3 clinical trials including trial start up, conduct and close out activities.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;br\u0026gt;\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;MAJOR DUTIES \u0026amp;amp; \u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;RESPONSIBILITIES:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Trial Management: \u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the primary contact for managing protocol execution, including oversight of the CRO, other study service providers, and consultants that are involved in a clinical trial\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead cross-functional study execution team in support of study deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support establishment of study milestones and ensure accurate tracking and reporting of study metrics and timelines to leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure clinical trials are managed and executed in accordance with ICH GCP, regulations, the protocol, and company-specific SOPs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in preparation and review of clinical trial documentation such as; protocol, informed consent, Investigator Brochure, Clinical Monitoring Plan, Project Plan, Case Report Forms, Statistical Analysis Plan, Clinical Study Reports, and other study level documents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure that the Trial Master File (TMF) is set up and maintained appropriately throughout the trial, including periodic reviews\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate and coordinate resolution of audit finding and ensures audit-ready condition of clinical trial documentation including central clinical files\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participates in service provider selection process as a part of outsourcing activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identifies, with the support and guidance from Senior Clinical Operations staff, and supports development of plans and resolution of project issues and participates in process improvement initiatives as required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Supports\u0026amp;nbsp;assessing operational feasibility, recommending study execution plan and site selection under the Director of Clinical Operations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for the selection and study specific training of CRO study staff, monitors, investigational sites, and service providers\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In conjunction with legal \u0026amp;nbsp;group, \u0026amp;nbsp;facilitate \u0026amp;nbsp;the \u0026amp;nbsp;development \u0026amp;nbsp;of \u0026amp;nbsp;clinical \u0026amp;nbsp;trial agreements and other relevant documents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage clinical trial budgets, providing ongoing financial reporting and projections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Negotiate and finalize site contracts and budgets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform and manage data review process on an ongoing basis\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform site visits including site qualification, initiation, monitoring and close-out visits, as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee outsourced monitoring by reviewing, monitoring reports to ensure quality and resolution of site-related issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensures tracking and review of protocol deviations and assesses impact on study data\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develops and manages study budget and maintain within financial goals; Reviews and approves clinical invoices against approved budget\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provides oversight for forecasting of clinical supplies, including study drug and supplies\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;u\u0026gt;Department Management: \u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;May manage and/or oversee work of junior Clinical Operations staff\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;May support development and review of Clinical SOPs and other department initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Travel as needed to sites, conferences, industry meetings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as may be assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;QUALIFICATIONS:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Education:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.A./B.S. degree\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Experience:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;6+ years of clinical research experience within the Biotech or similar industry, with at least 2 years directly supporting clinical trial management\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Other Qualifications/Skills:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;(non-technical and technical skills)\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial management; Strong clinical study management skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of, and experience with, regulatory framework applicable to interactions with HCPs, payers, advocacy and other business partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven clinical operational skills to direct protocol execution to ensure timeline, budget and quality metrics are met\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills to effectively disseminate information to project team and outside parties\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience reviewing trial plans including developing creative strategies for site monitoring, risk mitigation, trial budgets, site selection, and clinical supplies management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Clinical research knowledge and cross-functional understanding of clinical trial methodology\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational, conflict resolution, prioritization and negotiation skills \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability in creative problem-solving and exercising sound judgment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Team oriented and ability to effectively collaborate with study team, cross-functional team members, and external partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to handle a high volume of highly complex tasks within a given timeline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to develop Therapeutic Areas knowledge and expertise through internal training and external conference attendance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient computer skills, specifically with Microsoft Office Suite that include Word, Excel, PowerPoint, and Outlook\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of MS Project for development and update of clinical study timelines\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Travel: 5%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Physical Requirements and Working Conditions:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally, and all other sedentary criteria are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Base salary compensation range: $150,000 - 172,000\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Please note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135261005,"name":"432000 - Clinical Operations","child_ids":[],"parent_id":4006905005}],"offices":[{"id":4002254005,"name":"Remote","location":"United States","child_ids":[4054753005,4055982005,4055983005,4050218005,4050194005,4050195005,4050196005,4050207005,4050197005,4050198005,4050199005,4053980005,4050200005,4050202005,4050205005,4050201005,4050203005,4050204005,4050206005],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4701579005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4438539005,"location":{"name":"Remote, United States"},"metadata":null,"id":4701579005,"updated_at":"2026-06-01T17:45:33-04:00","requisition_id":"458","title":"Director, Clinical Operations (Lung Program)","company_name":"4D Molecular Therapeutics","first_published":"2026-06-01T17:28:51-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;GENERAL SUMMARY:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Provide strategic and operational leadership for global clinical trial execution across the 4DMT lung portfolio. This role is responsible for delivering clinical programs aligned with corporate timelines, budget, quality, and regulatory expectations while building scalable operational infrastructure appropriate for a fast-paced biotechnology environment. The Director, Clinical Operations will lead internal Clinical Operations teams and external partners/CROs and collaborate with external teams to ensure efficient, high-quality, inspection-ready execution of Phase 1–3 clinical studies.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This individual will serve as a key cross-functional leader and Clinical Operations subject matter expert, driving operational strategy, proactive risk mitigation, and execution excellence across global development programs.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;MAJOR DUTIES \u0026amp;amp; \u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;RESPONSIBILITIES:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute global clinical operations strategies aligned with corporate objectives, program timelines, budgets, quality standards, and regulatory requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic operational leadership for Phase 1–3 clinical trials, ensuring efficient and compliant study execution across multiple global programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead sponsor-side oversight and governance of CROs and critical vendors, including vendor selection, performance management, issue escalation, quality oversight, budget accountability, and operational delivery.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactively identify, assess, and mitigate operational risks impacting timelines, enrollment, quality, budget, or regulatory compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive operational scalability and process optimization while maintaining execution excellence in a lean, fast-paced biotechnology environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and oversee global study timelines, resourcing strategies, and organizational planning across multiple dynamic programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build, mentor, and lead high-performing Clinical Operations teams, including hiring, talent development, performance management, and organizational growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with Therapeutic Area Heads (TAHs), Project Team Leaders (PTLs), Clinical Science, Regulatory Affairs, Biometrics, Quality, and other cross-functional stakeholders to ensure aligned program execution and timely decision-making.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as Clinical Operations representative and subject matter expert on cross-functional product development teams and governance committees.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide operational leadership and support for clinical trial protocol development, feasibility assessments, country and site strategy, enrollment planning, and study startup activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead Clinical Operations contributions to annual budget planning, quarterly forecasting, resource planning, and financial oversight for assigned programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure continuous inspection readiness across clinical programs, including oversight of TMF quality, audit preparedness, CAPA management, and health authority inspection support.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with Quality Assurance to maintain compliance with GCP, FDA, EMA, PMDA, ICH, and other applicable regulatory requirements and quality standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Regulatory Affairs and Clinical Science to support regulatory submissions and ongoing compliance requirements, including ClinicalTrials.gov disclosures and global regulatory obligations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute operational expertise to business development and due diligence activities, as applicable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and present program updates, operational metrics, key risks, and mitigation strategies to senior leadership and executive management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development, implementation, and continuous improvement of SOPs, operational processes, and scalable infrastructure to support organizational growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foster a culture of accountability, collaboration, operational excellence, and clear cross-functional communication.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Core Competencies, Knowledge \u0026amp;amp; Skill Requirements\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated leadership in sponsor-side clinical operations within biotechnology and/or pharmaceutical environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to lead global Phase 2 and/or Phase 3 clinical trials with accountability for operational delivery.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience managing CROs and external vendors from the sponsor perspective.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to influence cross-functional stakeholders and drive decision-making in ambiguous or rapidly evolving environments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong operational and strategic leadership skills with ability to balance high-level portfolio strategy and detailed execution oversight.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to proactively identify operational risks and implement effective mitigation strategies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to recruit, develop, retain, and motivate high-performing Clinical Operations teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong financial acumen with experience managing clinical trial budgets, forecasts, and resource planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep understanding of FDA, EMA, PMDA, ICH-GCP guidelines, and global clinical trial regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting inspection readiness activities, audits, and regulatory inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational skills with the ability to manage multiple complex global programs simultaneously.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication, presentation, negotiation, and interpersonal skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to operate effectively in a lean, fast-paced, and evolving biotechnology environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;High degree of accountability, ownership, adaptability, and execution focus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Communication \u0026amp;amp; Interpersonal Skills\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal, written, and presentation skills.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to communicate complex operational information clearly and concisely to technical and non-technical audiences, including executive leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong collaboration and relationship-building skills across internal teams and external partners.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to influence without authority and drive alignment across cross-functional stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;QUALIFICATIONS: \u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Education:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S./B.A. in Life Science or related discipline\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree (M.S./M.A., MPH, MHS, MBA) preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Experience:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.A./B.S. with 10+ years of applicable industry experience (Clinical Operations) in drug development, or advanced degree with 6+ years of experience across both early (Phase 1 or 2) and/or late-stage (Phase 3)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3+ years in a leadership role and with a minimum of 3+ years direct line management experience. \u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Relevant experience in clinical trial execution across all phases.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Other Qualifications/Skills:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to recruit, retain, organize, and motivate clinical operations personnel\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to communicate to leadership team on Clinical Operations updates and priorities as well as to advocate for required budget and resources\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage and oversee large scale programs that have corporate-wide impact\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to develop and manage functional and clinical trial-specific budgets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be self-motivating; prioritize and manage a large volume of work; show attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills are essential as this individual will partner with various team members and functional groups for clinical trials and business performance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Thorough knowledge and understanding of FDA and ICH Guidelines, GCP, medical terminology, and clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to be flexible and adaptable to changing business needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and interpersonal skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to write clearly and summarize information effectively\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Must be able to present complex information to various audiences\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Base salary compensation range:\u0026amp;nbsp;\u0026lt;strong\u0026gt;$225,000 - 250,000\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Please note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135261005,"name":"432000 - Clinical Operations","child_ids":[],"parent_id":4006905005}],"offices":[{"id":4002254005,"name":"Remote","location":"United States","child_ids":[4054753005,4055982005,4055983005,4050218005,4050194005,4050195005,4050196005,4050207005,4050197005,4050198005,4050199005,4053980005,4050200005,4050202005,4050205005,4050201005,4050203005,4050204005,4050206005],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4687837005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4431815005,"location":{"name":"Remote, United States"},"metadata":null,"id":4687837005,"updated_at":"2026-04-22T16:40:21-04:00","requisition_id":"426","title":"Director, Clinical Quality Assurance (CQA)","company_name":"4D Molecular Therapeutics","first_published":"2026-04-22T16:40:21-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;GENERAL SUMMARY\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director of Clinical Quality Assurance (CQA) will be responsible for Quality Assurance oversight of multiple, global, 4DMT sponsored clinical trials, ensuring trials are executed in compliance with all applicable international regulatory requirements for Good Clinical Practice (GCP). This position reports to the Senior Director, GCP Compliance and Quality Systems and contributes to the development, implementation, and successful execution of the CQA mission, objectives, and strategic plan.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;MAJOR DUTIES \u0026amp;amp; \u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;RESPONSIBILITIES:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Provide Quality oversight for multiple 4DMT Clinical Studies, including the following \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;study-specific activities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement Clinical Study Quality Plans for specific 4DMT clinical studies,\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;focused on ensuring subject safety/rights, study data integrity, and GCP compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide guidance and support to clinical study teams, including via attendance at Study\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;team meetings and via investigation and management of Clinical Study Quality Events\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure principles of Risk Management are applied to the Clinical Study per ICH E6\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify, communicate, and escalate significant incidents of GCP non-compliance and\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;follow to resolution, acting at all times with an appropriate sense of urgency\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan, perform, and/or oversee GCP Compliance audits of high-risk clinical vendors/sites,\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;including clinical investigator sites\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure audit findings are communicated to audit stakeholders and collaborate with auditees and vendors to track, review, approve, and assess the adequacy of CAPAs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform Clinical Document reviews, ensuring the quality, accuracy and completeness of various documents, including as applicable Clinical Protocols, IBs, DSURs, Module 2.6 Tabulated and Written Summaries, and Integrated Summaries\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Support investigation and management of specific Clinical Study Quality Events as \u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;assigned:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Monitor, track, and facilitate the completion of formal corrective and preventive actions (CAPAs) to address identified Clinical Study Quality Events, including potential serious breaches of GCP.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Support a quality-focused work environment in Clinical that fosters learning, respect, open communication, collaboration, integration, and teamwork:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Work with Clinical stakeholders to develop GCP compliance training materials and conduct training\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Clinical team to review, update and maintain related SOPs, identify the need for new SOPs, and support the review of new SOPs as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work with Clinical stakeholders to support Training, Development, and Implementation of 4DMT Clinical Study Risk Management Process/Tools to ensure principles of Risk Management are applied to 4DMT Clinical Studies per ICH E6\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive the development and continuous improvement of the Clinical Quality Management System through the development / refinement of Clinical QA processes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Support preparedness / readiness / management of BIMO inspections:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop/support GCP inspectional readiness plans and lead inspectional readiness activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Host and/or assist with management of GCP-related inspections\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with GMP Quality and Clinical Operations teams to facilitate the investigation of clinical supply quality issues such as temperature excursions, product complaints and deviations reported from clinical sites.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;QUALIFICATIONS:\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Education:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;S./B.A. degree in a science or related life science field or equivalent; advanced scientific degree preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Experience:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years of experience or advanced degree with 7+ years of experience within a regulated environment such as Regulatory, Quality, Pharmacovigilance or Clinical Development / Operations within the Biotech or similar Industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience with GCP Quality Management Systems, quality support, and quality oversight of global clinical trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum of 4 years of significant experience in clinical quality assurance, including experience performing/supporting GCP audits and overseeing global clinical trials, including in APAC.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive practical experience and understanding of clinical quality assurance as applied throughout the clinical development life-cycle\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;(Optional) 5+ years of management experience or other specific work experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Other Qualifications/Skills:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;In-depth understanding of GCP requirements for investigational products\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills, both oral and written\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal skills, collaborative approach essential\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable in a fast-paced small company environment with minimal direction and able to adjust to workload based upon changing priorities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Travel: %5\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Physical Requirements and Working Conditions:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally, and all other sedentary criteria are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Base salary compensation range:\u0026amp;nbsp;\u0026lt;strong\u0026gt;$205,000 - $235,000\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Please note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135266005,"name":"452000 - Quality","child_ids":[],"parent_id":4006905005}],"offices":[{"id":4002254005,"name":"Remote","location":"United States","child_ids":[4054753005,4055982005,4055983005,4050218005,4050194005,4050195005,4050196005,4050207005,4050197005,4050198005,4050199005,4053980005,4050200005,4050202005,4050205005,4050201005,4050203005,4050204005,4050206005],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4689975005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4432897005,"location":{"name":"Emeryville, California"},"metadata":null,"id":4689975005,"updated_at":"2026-05-19T11:26:53-04:00","requisition_id":"450","title":"Director, Financial Planning and Analysis ","company_name":"4D Molecular Therapeutics","first_published":"2026-04-29T23:52:13-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;GENERAL SUMMARY\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director, FP\u0026amp;amp;A – TechOps serves as the primary finance business partner to the TechOps organization, providing end‑to‑end financial leadership across Manufacturing, Supply Chain, CMC Quality, and External Manufacturing as 4DMT transitions from late‑stage clinical development to commercial readiness and launch. This role is responsible for driving financial planning, forecasting, and decision support for a rapidly scaling TechOps organization. The Director will partner closely with TechOps leadership to translate operational plans into clear financial outcomes, proactively manage risks, and enable disciplined, data‑driven decisions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The position is expected to operate as a hands‑on, strategic individual contributor, with future people management potential as the organization scales.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Director role will report to the CFO and is expected on site\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;MAJOR DUTIES \u0026amp;amp; RESPONSIBILITIES:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Act as the primary finance partner to TechOps leadership, supporting strategic planning, operational decisions, and investment prioritization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Translate TechOps strategy, timelines, and operating plans into financial forecasts with implications, trade‑offs, and scenarios\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own the TechOps annual budget, rolling forecast, and long‑range plan inputs through close coordination with business partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and maintain detailed spend, headcount, and models aligned to clinical needs, manufacturing runs and launch timelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure financial plans accurately reflect changes in demand, supply constraints, tech transfers, and scale‑up activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead scenario and sensitivity analyses to assess financial impact of operational risks and strategic alternatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deliver clear monthly variance analysis, forecasting updates, and KPI reporting for TechOps leadership and Finance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support company‑wide cash flow forecasting and runway modeling, with particular focus on timelines and spend phasing\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;QUALIFICATIONS:\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Education:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree in Accounting, Finance, or related field; CPA or MBA preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Experience:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years of progressive experience in FP\u0026amp;amp;A roles\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior biotech, pharmaceutical, or life sciences experience required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting a late‑stage clinical development organization through commercial launch (ideally first global product launch) required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with ERP selection and implementation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience partnering with TechOps, Manufacturing, Supply Chain, and/or CMC organizations required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Understanding of CMC processes (e.g. upstream, downstream, fill finish, pack and label, etc)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience partnering with Clinical Development is a plus\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Skills:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in finance software (e.g., NetSuite, Adaptive) and Microsoft Excel\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong analytical and problem-solving skills, with the ability to interpret complex financial data and trends\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication and interpersonal skills, with the ability to collaborate effectively across functional teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Detail-oriented, organized, and able to manage multiple priorities in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Travel: \u0026amp;lt;5%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Physical Requirements and Working Conditions:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Base salary compensation range: \u0026lt;strong\u0026gt;$237,000 - 263,000\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Please note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135243005,"name":"831000 - Finance","child_ids":[],"parent_id":4006947005}],"offices":[{"id":4006441005,"name":"Hybrid","location":"Emeryville, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4690434005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4433013005,"location":{"name":"Remote, United States"},"metadata":null,"id":4690434005,"updated_at":"2026-04-29T18:23:46-04:00","requisition_id":"451","title":"Executive Director, Preclinical and Translational Sciences","company_name":"4D Molecular Therapeutics","first_published":"2026-04-29T17:23:29-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;GENERAL SUMMARY\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This Executive Director position will report to the Senior Vice President, Research \u0026amp;amp; Early-Stage Product Development and lead a team of translational scientists and drug development experts tasked with bringing innovative gene therapies to patients.\u0026amp;nbsp; The incumbent will have a high level of passion for 4DMT’s mission and the ability to operate as an effective strategic and tactical thinker. They will also be effective as a hands-on manager and supervisor of individual work. Candidates should have a PhD or MD/PhD degree (or equivalent) in Biological Sciences or a related discipline, with significant experience in pharmaceutical research and development.\u0026amp;nbsp; They will lead a preclinical and translational group responsible for: (1) developing target-engagement biomarkers and clinical biomarkers with relevance to Proof of Concept (POC) gene therapy studies, (2) conducting laboratory and in silico analyses of biomarker readouts generated in the relevant Phase 1 and Phase 2 gene therapy studies, (3) performing immunological assays and analyses relevant to detecting host immune responses to 4DMT gene therapy vectors in the clinical trial setting, and (4) overseeing outsourced performance of preclinical pharmacology and toxicology studies of 4DMT gene therapy vectors, in partnership with external CROs. This role will interact and collaborate with multiple functions at 4DMT, including but not limited to Clinical Science and Operations, Regulatory Affairs, Discovery \u0026amp;amp; Innovation, Commercial, and CMC.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;MAJOR DUTIES \u0026amp;amp; RESPONSIBILITIES:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Set, communicate and drive strategy for Translational products in alignment with the broader organization of 4DMT\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prioritize and allocate resources, both within Translational and beyond, to meet portfolio needs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead the decision-making process with other relevant functional group heads regarding indications, targets and products’ progression from concept, design, preclinical development and Phase 1-2 clinical testing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide input on scientific strategy from the earliest consideration of new targets through development, including risk, scientific challenges, timing of resource investment and development of go/no go decisions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;‪Direct and coordinate the implementation of preclinical study programs for pharmacology studies in support of the lead to candidate optimization process\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;‪Design, implement and write-up comprehensive series of pharmacology studies to address preclinical exposure, develop pharmacokinetics and pharmacodynamics profiles and generate GLP toxicology and bio-distribution packages suitable for supporting IND filings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage budgets and headcounts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;‪Design, implement and manage externally facing in vivo studies with CROs and academic centers, including drafting proposals, budget oversight and managing deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Resource planning; hiring and mentoring talents; building the team and technical capabilities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build collaborations with relevant functions at 4DMT; represent own function at the corporate level and externally\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide direct hands-on responsibility for all Translational interactions as well as grant writing and management with rare disease advocacy groups\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Participate on project teams and direct activities to ensure regulatory compliance of pre-clinical and clinical research activities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support regulatory affairs in their preparation, review and submission of necessary pre-clinical and clinical regulatory information to regulatory agencies worldwide\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to defining of clear human POC study outcome criteria for decision-making on new product candidates\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute senior level expertise to alliance, business development, due diligence exercises with external entities and licensing meetings as well as other critical external interfaces such as public health regulatory bodies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned, nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;QUALIFICATIONS:\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Education:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD, MD/PhD, MD or equivalent\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Experience:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;12+ years of relevant preclinical and/or translational sciences experience within the Biotech or similar industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;4+ years of management experience or other specific work experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with preclinical, translational, and clinical R\u0026amp;amp;D\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior leadership position/s within the pharmaceutical/biotech industry or academic medical centers, with a significant history of research and translational experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Reputation for inspiring a culture of continuous improvement, innovation and quality, leading and mentoring at the highest level of achievement\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Skills:\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Team leadership skills and experience in a matrixed organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to support and impact experts, scientists and project deliverables across functions in research, development and beyond\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication skills both written and oral with demonstrated ability to present ideas, information, and data effectively via one-on-one discussions, team meetings, and presentations to executive leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent time management skills (schedules, timelines, task prioritization) and the ability to adapt to changing priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-starter who proactively establishes effective working relationships and builds partnerships with other disciplines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adaptability, flexibility, independence and resourcefulness; as an active participant in a vibrant small company culture, rolls up sleeves and manages multiple activities in parallel.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to proactively identify challenges; possesses strategic foresight and implements appropriate courses of action\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent verbal and written communication skills\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Travel: 5-10%\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Physical Requirements and Working Conditions:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Base salary compensation range: \u0026lt;strong\u0026gt;$270,000 - 342,000\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Please note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4147074005,"name":"4325 Clinical Science - Lung","child_ids":[],"parent_id":4135260005}],"offices":[{"id":4002254005,"name":"Remote","location":"United States","child_ids":[4054753005,4055982005,4055983005,4050218005,4050194005,4050195005,4050196005,4050207005,4050197005,4050198005,4050199005,4053980005,4050200005,4050202005,4050205005,4050201005,4050203005,4050204005,4050206005],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4691301005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4433316005,"location":{"name":"Remote, United States"},"metadata":null,"id":4691301005,"updated_at":"2026-04-30T17:25:11-04:00","requisition_id":"423","title":"Principal Medical Writer","company_name":"4D Molecular Therapeutics","first_published":"2026-04-30T17:25:11-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;GENERAL SUMMARY:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Principal Medical Writer will support 4D‑150, a gene therapy in late-stage development for retinal vascular diseases, including nAMD and DME, and associated BLA‑enabling activities as well as clinical stage work within the lung program. This role is responsible for the planning, development, and delivery of high‑quality clinical and regulatory documents across late‑stage development, working closely with Clinical Science, Clinical Operations, Data Science, Regulatory Affairs, Quality, and external partners. This role is expected to play a central role in BLA readiness, including oversight of the development, coordination, and execution of key BLA modules, and management of internal and external medical writing resources to ensure timely, high‑quality regulatory deliverables.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate brings strong late clinical‑stage medical writing experience, demonstrated ability to manage complex timelines, and a deep understanding of regulatory expectations for global Phase 3 programs and BLA readiness.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;MAJOR DUTIES \u0026amp;amp; RESPONSIBILITIES:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide oversight for the planning, development, and execution of BLA modules, working closely with Clinical Science, Regulatory Affairs, Data Science, and Quality to ensure alignment with submission strategy and timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead and coordinate external medical writers and vendors, including selection, scope definition, timeline management, content review, and quality oversight.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure consistency, scientific accuracy, and regulatory alignment across BLA components and supporting clinical documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a key point of integration between internal subject matter experts and external writing resources to support efficient document development and review cycles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author, review, and coordinate key clinical and regulatory documents for the 4D‑150 Phase 3 program as well as for the early-phase lung program, including but not limited to protocols, protocol amendments, CSRs, IBs, DMC materials, briefing documents, and BLA‑enabling content.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead document planning and timeline management in collaboration with cross‑functional teams to support aggressive development milestones.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure consistency, clarity, and scientific accuracy across clinical documents, aligning with regulatory standards and internal expectations for quality.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with Clinical Science, Biostatistics, and Clinical Operations to integrate data interpretations, safety narratives, and efficacy analyses.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage document review cycles, address comments, and ensure timely resolution of feedback from internal stakeholders and external vendors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain document version control and adherence to internal SOPs, templates, and quality standards.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to continuous improvement of writing processes, tools, and templates to support scale‑up of late‑stage development activities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;QUALIFICATIONS:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;strong\u0026gt;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Education\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Advanced degree in life sciences (MS, PhD, PharmD, MD) preferred; Bachelor’s degree required.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Experience\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;5+ years of medical or clinical writing experience in biotech, pharmaceutical, or CRO settings.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Direct experience supporting Phase 3 clinical trials required; direct experience supporting early clinical trials (Phase 1/2) preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience authoring or contributing to BLA‑enabling documents strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Other Qualifications / Skills\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of ICH guidelines, FDA regulatory expectations, and clinical development processes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to manage multiple complex deliverables under tight timelines.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written communication skills with attention to scientific detail and clarity.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to work effectively in a fast‑paced, cross‑functional environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in gene therapy is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with leveraging AI-enabled tools to aid in document authoring is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Minimal; occasional travel (\u0026amp;lt;10%) as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements and Working Conditions:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Sedentary work involving extended periods of sitting, typing, and screen use. Repetitive hand and finger movements required. Virtual meetings may occur across time zones.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Base salary compensation range: \u0026lt;strong\u0026gt;$180,000 - 202,000\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Please note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135260005,"name":"431000 - Clinical Science","child_ids":[4147074005],"parent_id":4006905005}],"offices":[{"id":4002254005,"name":"Remote","location":"United States","child_ids":[4054753005,4055982005,4055983005,4050218005,4050194005,4050195005,4050196005,4050207005,4050197005,4050198005,4050199005,4053980005,4050200005,4050202005,4050205005,4050201005,4050203005,4050204005,4050206005],"parent_id":null}]},{"absolute_url":"https://4dmoleculartherapeutics.com/careers/?gh_jid=4702802005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"education":"education_required","internal_job_id":4439156005,"location":{"name":"Emeryville, California"},"metadata":null,"id":4702802005,"updated_at":"2026-06-04T17:00:27-04:00","requisition_id":"459","title":"Senior Quality Specialist (Contract)","company_name":"4D Molecular Therapeutics","first_published":"2026-06-04T16:59:39-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;em\u0026gt;Attention recruitment agencies:\u0026lt;/em\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;em\u0026gt; All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;GENERAL SUMMARY\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;4DMT is hiring a Sr. Quality Specialist, Document \u0026amp;amp; Records Management. Reporting to the Senior Manager, Quality Document \u0026amp;amp; Records Management, the Sr. Quality Specialist will be responsible for ensuring 4DMT\u0026#39;s Quality Document \u0026amp;amp; Records Management is designed and executed in an efficient, compliant, and inspection ready manner.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This individual will support the Senior Manager, Quality Document \u0026amp;amp; Records Management for the quality document and records management system, ensuring compliance with applicable GxP regulations, industry standards, and internal policies. In addition to driving process improvements and system optimization, this role will perform operational tasks to support document and record lifecycles.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is hybrid and will require regularly scheduled time on-site at 4DMT\u0026#39;s Emeryville office at least 3x a week.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;RESPONSIBILITIES:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Quality Document Control \u0026amp;amp; Records Management System - 50% of the time:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the point of contact for the Document Control system and quality-controlled records management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the development, enforcement, and improvement of policies, procedures, work instructions, templates, and forms related to document and records management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate closely with stakeholders (e.g., legal, clinical, regulatory, IT) to align record policies and lifecycles across platforms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support centralized and decentralized quality-controlled record repositories (physical and electronic) for completeness, integrity, and retrievability.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support inspection readiness by ensuring all quality-controlled records are accessible, traceable, and compliant with data integrity and protection requirements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support record audits, gap assessments, and remediation plans in preparation for regulatory inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Monitor, trend and report document control metrics (e.g., cycle time, overdue documents)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support internal and external audits and inspections.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide guidance and training to system users and support documentation governance across departments.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Other duties as assigned, nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Quality Document Control \u0026amp;amp; Records Management Operations - 50% of the time:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Perform document intake, advanced formatting, metadata review, routing, publishing, and obsoletion and ensure timely review, approval, and release.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support the management of periodic reviews of controlled documents.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advise document control participants on content and format to meet 4DMT procedural requirements, standards, templates, and best practices.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with document control procedures and applicable regulations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Quality Training to coordinate document and training lifecycles.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Facilitate quality-controlled records management (e.g., onsite and off-site secure storage, retention, destruction)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and implement innovative methods to increase efficiency of operational tasks.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;QUALIFICATIONS:\u0026amp;nbsp;\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Education:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required, preferably in a scientific, technical, or related field.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Experience:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;6+ years of experience in document control and records management within the biotech, pharmaceutical, or medical device industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years in a hands-on system and/or process ownership role for a GxP EDMS (e.g., ACE, MasterControl, Veeva, etc.).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2+ years leading or supporting GxP records management operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comprehensive knowledge of FDA, EMA, ICH requirements and industry best practices for document control and records management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Practical experience leading or actively participating in at least 1 EDMS or EQMS system implementation and/or significant enhancement project.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exposure to audits and health authority inspections ideally in a commercializing biotech environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Domain knowledge of clinical research and development, manufacturing, quality, and/or IT is highly desirable.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Skills:\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience in document formatting using MS Word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid working proficiency in other productivity tools (e.g., Outlook, Teams, SharePoint, Excel, PowerPoint, Forms, DocuSign, Adobe Acrobat).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Basic knowledge of or willing to learn analytical and reporting tools (e.g., PowerBI).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Foundational understanding of change management principles\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Key Competencies\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Excellent interpersonal communication skills both written and verbal.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized with the ability to multi-task and perform effectively under pressure.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven project management, problem-solving, and organizational skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to collaborate, influence, and negotiate effectively.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Motivated to seek out training and mentorship for professional development.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Travel\u0026lt;/strong\u0026gt;: 75%, to Emeryville.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Physical Requirements and Working Conditions:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Physical Activity - Repetitive motions: Making substantial movements (motions) of the wrists, hands, and/or fingers. Fingering: Picking, pinching, typing or otherwise working, primarily with fingers rather than with whole hand or arm as in handling. Talking: Expressing or exchanging ideas by means of the spoken word.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Physical Requirements - Sedentary work: Exerting up to 10 - 20 pounds of force occasionally and/or a negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working Conditions - The worker is not substantially exposed to adverse environmental conditions (as in typical office or administrative work).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Hourly compensation range: $51.00 - 64.00\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Please note, the hourly compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div\u0026gt;4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4135266005,"name":"452000 - Quality","child_ids":[],"parent_id":4006905005}],"offices":[{"id":4002254005,"name":"Remote","location":"United States","child_ids":[4054753005,4055982005,4055983005,4050218005,4050194005,4050195005,4050196005,4050207005,4050197005,4050198005,4050199005,4053980005,4050200005,4050202005,4050205005,4050201005,4050203005,4050204005,4050206005],"parent_id":null}]}],"meta":{"total":11}}