{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/epicbio/jobs/6007685004","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":5159403004,"location":{"name":"South San Francisco, California, United States"},"metadata":null,"id":6007685004,"updated_at":"2026-05-27T17:48:53-04:00","requisition_id":"180","title":"Associate Scientist, Downstream Process Development","company_name":"Epicrispr Biotechnologies","first_published":"2026-05-27T17:48:53-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;Who Are We?\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_19\u0026quot;\u0026gt;Our company is based on the science of our founder, Stanley Qi, one of the original CRISPR co-inventors who then furthered the technology so that DNA does not need to be cut to accomplish gene regulation. Instead, we regulate the epigenome to suppress and activate multiple genes simultaneously. We are further evolving the platform and leveraging its strengths to address unmet medical needs.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;We are looking for exceptional team members who want an active role in building a rapidly growing biotech.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Title:\u0026lt;/strong\u0026gt; Associate Scientist, Downstream Process Development\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location\u0026lt;/strong\u0026gt;: South San Francisco, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Opportunity:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We are seeking a highly motivated and detail-oriented Associate Scientist to join the Downstream Process Development team focused on adeno-associated virus (AAV) gene therapy therapeutics. This role will support the development, optimization, and scale-up of purification processes for AAV vectors from early research through clinical manufacturing.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Responsibilities:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Design, execute, and analyze downstream purification experiments for AAV vectors for process steps including clarification, sterile filtration, tangential flow filtration (TFF), chromatography (affinity, ion exchange, size exclusion, mixed mode), and ultracentrifugation.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform small-scale studies for development of downstream AAV processes, process optimization, process characterization, and assessment of process robustness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support process development activities from bench scale through pilot scale and tech transfer to GMP manufacturing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present data and project updates in team meetings and cross-functional forums.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate and timely documentation in electronic lab notebooks and technical reports.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally with upstream process development and analytical development and other functions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay current with advancements in AAV purification technologies, regulatory expectations, and industry best practices.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications:\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;\u0026lt;em\u0026gt;The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S. degree in Biochemical Engineering, Chemical Engineering, Molecular Biology, Biotechnology, Biochemistry, or related discipline with 5+ years of relevant industry experience (or M.S. with 3+ years or Ph.D.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Required experience with AKTA purification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong working knowledge of chromatography and filtration technologies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with viral vector purification, preferably AAV\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with analytical techniques for AAV characterization such as Refeyn, qPCR/dPCR/ddPCR, ELISA, alkaline gel, CE-SDS, SEC-HPLC, AUC and other similar analytical assays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with Design of Experiments (DOE) and JMP are a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational, analytical, and problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent written and verbal communication skills\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Compensation: The salary range for this position is $118,000 to $124,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Epicrispr Biotechnologies is an early-stage biotechnology company developing a novel technology platform that can provide safe and persistent control of targeted gene regulation. Our proprietary platform represents an entirely new class of therapeutics that can be leveraged to treat severe disease across numerous therapeutic areas, including complex diseases impacted by multiple genes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Epicrispr Biotechnologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4049107004,"name":"ClinOps-CMC-Reg","child_ids":[],"parent_id":null}],"offices":[{"id":4027644004,"name":"Epicrispr Biotechnologies","location":"South San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/epicbio/jobs/6007701004","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":5159411004,"location":{"name":"South San Francisco, California, United States"},"metadata":null,"id":6007701004,"updated_at":"2026-05-27T18:28:32-04:00","requisition_id":"181","title":"Project Manager (CMC / Development Operations)","company_name":"Epicrispr Biotechnologies","first_published":"2026-05-27T18:28:32-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;Who Are We?\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_19\u0026quot;\u0026gt;Our company is based on the science of our founder, Stanley Qi, one of the original CRISPR co-inventors who then furthered the technology so that DNA does not need to be cut to accomplish gene regulation. Instead, we regulate the epigenome to suppress and activate multiple genes simultaneously. We are further evolving the platform and leveraging its strengths to address unmet medical needs.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;We are looking for exceptional team members who want an active role in building a rapidly growing biotech.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Position:\u0026lt;/strong\u0026gt; Project Manager (CMC / Development Operations)\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Location: \u0026lt;/strong\u0026gt;South San Francisco, CA\u0026lt;br\u0026gt;Remote, Hybrid and In Person options\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Opportunity\u0026lt;/span\u0026gt;:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Epicrispr Biotechnologies is seeking a highly organized and proactive Project Manager to support execution of CMC and cross-functional development programs. This role will initially focus heavily on CMC project management, including oversight of manufacturing activities at CMOs, and will expand over time to support broader product development initiatives across the organization.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Roles and Responsibilities\u0026lt;/span\u0026gt;:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee execution of manufacturing runs at Contract Manufacturing Organizations (CMOs) for lead programs, including tracking completion of action items, monitoring program activities and milestones, and driving resolution of risks and issues across the cross-functional team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as key alliance manager for CMC vendors in partnership with the VP of Tech Ops, ensuring effective collaboration and execution across external partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track and maintain visibility of program timelines, dependencies, and deliverables across CMC and broader development workstreams using appropriate tracking tools\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organize, schedule, and facilitate internal cross-functional program meetings to ensure alignment and clear communication across teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain, organize, and continuously improve program documentation, trackers, and repositories (e.g., Smartsheet, SharePoint)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Document key decisions, risks, assumptions, issues, action items, and overall program plans in a clear and structured manner\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide clear, timely communication of program status updates, risks, and key decisions to leadership and relevant stakeholders\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate across CMC, Clinical, Regulatory, and Nonclinical teams to ensure alignment and execution of integrated program deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support planning and coordination of key nonclinical and regulatory milestones as needed to enable program execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with the Associate Director to identify, develop, and implement opportunities to streamline and standardize project management processes, tools, and workflows across Epicrispr\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help build scalable project management infrastructure that improves visibility, accountability, and execution discipline across programs and teams\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Requirements\u0026lt;/span\u0026gt;:\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; Master’s degree preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;3–7+ years of experience in project or program management within biotechnology, pharmaceutical, or life sciences environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong experience in CMC, manufacturing, or technical operations preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with project tracking tools such as Smartsheet and SharePoint\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational, communication, and documentation skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities in a fast-paced, dynamic environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail and commitment to follow-through and accountability\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable working in ambiguous, early-stage biotech environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong interpersonal skills with the ability to collaborate across technical and non-technical teams\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage conflict and remain composed under pressure\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in startup or rapidly scaling biotech environments is a plus\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Compensation: The salary range for this position is $140,000 to $150,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Epicrispr Biotechnologies is an early-stage biotechnology company developing a novel technology platform that can provide safe and persistent control of targeted gene regulation. Our proprietary platform represents an entirely new class of therapeutics that can be leveraged to treat severe disease across numerous therapeutic areas, including complex diseases impacted by multiple genes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Epicrispr Biotechnologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4049107004,"name":"ClinOps-CMC-Reg","child_ids":[],"parent_id":null}],"offices":[{"id":4027644004,"name":"Epicrispr Biotechnologies","location":"South San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/epicbio/jobs/5971188004","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":5142790004,"location":{"name":"South San Francisco, California, United States"},"metadata":null,"id":5971188004,"updated_at":"2026-04-28T18:43:27-04:00","requisition_id":"176","title":"Research Associate II/Senior Research Associate, Process Development","company_name":"Epicrispr Biotechnologies","first_published":"2026-04-15T18:44:36-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;Who Are We?\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_19\u0026quot;\u0026gt;Our company is based on the science of our founder, Stanley Qi, one of the original CRISPR co-inventors who then furthered the technology so that DNA does not need to be cut to accomplish gene regulation. Instead, we regulate the epigenome to suppress and activate multiple genes simultaneously. We are further evolving the platform and leveraging its strengths to address unmet medical needs.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;We are looking for exceptional team members who want an active role in building a rapidly growing biotech.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Title: Research Associate II/Senior Research Associate, Process Development\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Location: South San Francisco, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Opportunity:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Epicrispr Biotechnologies is seeking a highly motivated Senior Research Associate to join our Process Development team. This individual will contribute to the development and optimization of our in-house AAV platform, support preclinical vector supply, and play an active role in day-to-day lab operations. The ideal candidate is a hands-on experimentalist with strong experience in mammalian cell culture and viral vector production, who thrives in a fast-paced, collaborative startup environment. This role will support the development of scalable and robust processes to advance our gene regulation platform.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Roles and Responsibilities:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute upstream AAV production (2-5L) using transient transfection in suspension cell culture, supporting iterative process improvements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct studies to develop representative scale-down models for manufacturing processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to DoE studies (shake flasks) and process characterization experiments to evaluate and define critical process parameters (CPPs) and assess their impact on critical quality attributes (CQAs)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support upstream production campaigns to meet preclinical material demands on schedule and within quality expectations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist in generating and analyzing data sets to support process development reports, tech transfer documents, and internal presentations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform and analyze dPCR and flow cytometry experiments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain thorough, accurate, and timely documentation of experimental methods, data, and results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support general lab operations including equipment maintenance, reagent and consumable inventory management, vendor coordination, and sample tracking\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate cross-functionally with Research, Analytical Development, and Manufacturing teams\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;Qualifications:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;B.S. degree in Cell Biology, Biochemistry, Biology, or a related discipline with 4+ years of relevant industry experience (or M.S. with 2+ years)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with mammalian cell culture (adherent and suspension), aseptic technique, and transient transfection\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated proficiency in benchtop bioreactor AAV production (inoculation through clarification)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with AAV or viral vector production\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with analytical methods such as PCR/dPCR and flow cytometry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Solid data analysis skills with ability to interpret complex results, communicate findings, and recommend next steps\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with statistical design and analysis, including Design of Experiments (DoE), is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional attention to detail with proven excellence in experimental documentation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong critical thinking and creative problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Self-motivated, proactive and takes initiative when managing multiple priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative team player who communicates openly and effectively within department and cross-functionally\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prior experience in a startup environment is a plus\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Compensation: The salary range for this position is $80,000 to $108,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Epicrispr Biotechnologies is an early-stage biotechnology company developing a novel technology platform that can provide safe and persistent control of targeted gene regulation. Our proprietary platform represents an entirely new class of therapeutics that can be leveraged to treat severe disease across numerous therapeutic areas, including complex diseases impacted by multiple genes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Epicrispr Biotechnologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4049107004,"name":"ClinOps-CMC-Reg","child_ids":[],"parent_id":null}],"offices":[{"id":4027644004,"name":"Epicrispr Biotechnologies","location":"South San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/epicbio/jobs/5835104004","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":5067546004,"location":{"name":"South San Francisco, California, United States"},"metadata":null,"id":5835104004,"updated_at":"2026-04-28T09:58:50-04:00","requisition_id":"173","title":"Scientist I/ Scientist II, Bioanalytical","company_name":"Epicrispr Biotechnologies","first_published":"2026-04-20T17:08:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;Who Are We?\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_19\u0026quot;\u0026gt;Our company is based on the science of our founder, Stanley Qi, one of the original CRISPR co-inventors who then furthered the technology so that DNA does not need to be cut to accomplish gene regulation. Instead, we regulate the epigenome to suppress and activate multiple genes simultaneously. We are further evolving the platform and leveraging its strengths to address unmet medical needs.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;We are looking for exceptional team members who want an active role in building a rapidly growing biotech.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Title\u0026lt;/strong\u0026gt;: Scientist I/ Scientist II, Bioanalytical\u0026lt;br\u0026gt;\u0026lt;strong\u0026gt;Location\u0026lt;/strong\u0026gt;: South San Francisco, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Opportunity\u0026lt;/strong\u0026gt;:\u0026lt;br\u0026gt;Epicrispr Biotechnologies is seeking a motivated Scientist I / Scientist II, Bioanalytical to\u0026amp;nbsp;support the development and execution of bioanalytical strategies across our pipeline.\u0026amp;nbsp;This individual will contribute to advancing preclinical and clinical programs through\u0026amp;nbsp;hands-on assay development, biomarker analysis, and data generation. The ideal\u0026amp;nbsp;candidate is detail-oriented, collaborative, and excited to grow in a fast-paced biotech\u0026amp;nbsp;environment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Roles and Responsibilities\u0026lt;/strong\u0026gt;:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Design, develop, and execute bioanalytical assays to support preclinical and clinical studies, including PK/PD and biomarker assessments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform routine and complex experiments, analyze data, and clearly document results\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development of cell-based potency assays for early-stage and clinical programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot assays and optimize methods to improve performance and reproducibility\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain accurate and organized laboratory records and ensure data integrity\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with cross-functional teams including R\u0026amp;amp;D, Clinical Development, and Translational Sciences\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate with external CROs for sample analysis and timelines as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to regulatory documentation by supporting bioanalytical sections of INDs and other filings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Stay current with relevant technologies and apply new methods where appropriate\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present findings in team meetings and contribute to scientific discussions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with GLP/GCP standards and internal quality systems\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Qualifications\u0026lt;/strong\u0026gt;:\u0026lt;br\u0026gt;• Scientist I:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ph.D. in Biology, Pharmacology, Bioanalytical Chemistry, or related field,\u0026lt;br\u0026gt;or\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Master’s with 0–3+ years of relevant industry experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;• Scientist II:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Ph.D. with 2–5 years of relevant industry experience, \u0026lt;br\u0026gt;or\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Master’s with 4–7 years of relevant industry experience\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Skills\u0026lt;/strong\u0026gt;:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Hands-on experience with bioanalytical assay development and/or execution\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with techniques such as qPCR, digital PCR, ligand binding assays, LC-MS/MS, flow cytometry, and/or reporter gene assays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting gene therapy, cell therapy, or nucleic acid-based therapeutics is a plus\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Basic understanding of PK/PD principles and translational science\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong attention to detail and problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work both independently and collaboratively in a team environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective communication and organizational skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable working in a fast-paced, evolving environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Compensation: The salary range for this position is $124,000 to $148,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Epicrispr Biotechnologies is an early-stage biotechnology company developing a novel technology platform that can provide safe and persistent control of targeted gene regulation. Our proprietary platform represents an entirely new class of therapeutics that can be leveraged to treat severe disease across numerous therapeutic areas, including complex diseases impacted by multiple genes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Epicrispr Biotechnologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4044346004,"name":"Therapeutics","child_ids":[],"parent_id":null}],"offices":[{"id":4027644004,"name":"Epicrispr Biotechnologies","location":"South San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/epicbio/jobs/5986442004","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":5149445004,"location":{"name":"South San Francisco, California, United States"},"metadata":null,"id":5986442004,"updated_at":"2026-05-06T16:56:01-04:00","requisition_id":"177","title":"Senior Clinical Research Associate","company_name":"Epicrispr Biotechnologies","first_published":"2026-05-05T11:35:05-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;Who Are We?\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_19\u0026quot;\u0026gt;Our company is based on the science of our founder, Stanley Qi, one of the original CRISPR co-inventors who then furthered the technology so that DNA does not need to be cut to accomplish gene regulation. Instead, we regulate the epigenome to suppress and activate multiple genes simultaneously. We are further evolving the platform and leveraging its strengths to address unmet medical needs.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;We are looking for exceptional team members who want an active role in building a rapidly growing biotech.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Position: Senior Clinical Research Associate\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Location: South San Francisco, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Opportunity:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;br\u0026gt;Epicrispr Bio is seeking a detail-oriented and proactive Senior Clinical Research Associate (CRA) to support the execution and oversight of clinical trials. This role will play a key part in ensuring studies are conducted in compliance with regulatory requirements, GCP guidelines, and company protocols, while maintaining the highest standards of quality and data integrity.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The ideal candidate will bring a strong foundation in clinical operations, experience working cross-functionally with CROs and clinical teams, and the ability to independently manage site activities while contributing to process improvements in a fast-paced, growing environment. This is an opportunity to have meaningful impact on clinical development programs while helping to build and scale operational excellence within the organization.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;\u0026lt;u\u0026gt;Roles and Responsibilities:\u0026lt;/u\u0026gt;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Assist the Clinical Operations team with on-site sample operations, including sample receipt, registration, and shipments in a GCP environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support clinical trial manager with site management, including: site startup activities, co-monitoring visits alongside CRO, reviewing monitoring visit reports, coordinating vendor trainings, reviewing study newsletters, and other duties as needed, in alignment with study priorities and CTM guidance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assist clinical trial manager with data verification and ICF reviews as needed, alongside CRO, to support data quality and protocol compliance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with CTM and clinical team to help identify areas to improve our processes, with priorities defined by the CTM, and support implementation of agreed-upon improvements.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Identify and communicate site-level issues, protocol deviations, and operational risks to the CTM to support timely resolution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain study trackers, logs, and documentation across regulatory, site, data, and sample operations to support study oversight and execution.\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;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in life sciences or related field preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;2 - 5+ years of CRA or clinical research experience (biotech, pharma, or CRO environment)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of GCP, ICH guidelines, and clinical trial processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working with CROs and managing clinical sites\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational, communication, and problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities in a fast-paced environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Compensation: The salary range for this position is $115,000 to $121,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Epicrispr Biotechnologies is an early-stage biotechnology company developing a novel technology platform that can provide safe and persistent control of targeted gene regulation. Our proprietary platform represents an entirely new class of therapeutics that can be leveraged to treat severe disease across numerous therapeutic areas, including complex diseases impacted by multiple genes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Epicrispr Biotechnologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4049107004,"name":"ClinOps-CMC-Reg","child_ids":[],"parent_id":null}],"offices":[{"id":4027644004,"name":"Epicrispr Biotechnologies","location":"South San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/epicbio/jobs/5987839004","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":5150066004,"location":{"name":"South San Francisco, California, United States"},"metadata":null,"id":5987839004,"updated_at":"2026-05-06T18:37:25-04:00","requisition_id":"178","title":"Vendor \u0026 Budget Manager, Clinical Operations","company_name":"Epicrispr Biotechnologies","first_published":"2026-05-05T11:35:14-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;Who Are We?\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_19\u0026quot;\u0026gt;Our company is based on the science of our founder, Stanley Qi, one of the original CRISPR co-inventors who then furthered the technology so that DNA does not need to be cut to accomplish gene regulation. Instead, we regulate the epigenome to suppress and activate multiple genes simultaneously. We are further evolving the platform and leveraging its strengths to address unmet medical needs.\u0026amp;nbsp;\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;font_8\u0026quot;\u0026gt;\u0026lt;span class=\u0026quot;color_29\u0026quot;\u0026gt;We are looking for exceptional team members who want an active role in building a rapidly growing biotech.\u0026lt;/span\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;p\u0026gt;Position: Vendor \u0026amp;amp; Budget Manager, Clinical Operations\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Location: South San Francisco, CA\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Opportunity\u0026lt;/span\u0026gt;:\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Epicrispr Biotechnologies is seeking a \u0026lt;strong\u0026gt;Vendor and Budget Manager\u0026lt;/strong\u0026gt; to join our growing Clinical Operations team. This role will play a critical part in overseeing vendor relationships, contracts, and budgets to support the successful execution of our clinical programs. This is a highly cross-functional role partnering closely with Clinical Operations, Finance, Legal, and external vendors to ensure studies are executed efficiently and in alignment with timelines, scope, and budget.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Roles and Responsibilities\u0026lt;/span\u0026gt;:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Primary administrative point of contact for vendor coordination and\u0026amp;nbsp;communications, ensuring alignment with study priorities defined by\u0026amp;nbsp;Clinical Operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Handle logistical setup of new vendors including coordinating contract\u0026amp;nbsp;reviews with internal stakeholders and legal and budget negotiation, in\u0026amp;nbsp;alignment with study scope and requirements defined by Clinical\u0026amp;nbsp;Operations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage all existing clinical vendors, requiring contract oversight and\u0026amp;nbsp;coordination with legal and internal teams, budget and PO oversight\u0026amp;nbsp;alongside internal finance and accounting, while partnering with the CTM\u0026amp;nbsp;and other Clinical Operations team members to ensure vendor deliverables\u0026amp;nbsp;align with study needs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee site master budgets and ensure alignment with protocol updates,\u0026amp;nbsp;in coordination with CTM and Clin Ops priorities.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Approve vendor invoices and budgets, including pass throughs from CRO, ensuring consistency with agreed scopes of work and escalation of discrepancies as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support CMO, CTM, and Clinical Operations Lead with review of budget\u0026amp;nbsp;reporting from CRO alongside finance and accounting team.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track vendor performance, deliverables, contractual obligations, and\u0026amp;nbsp;escalate risks or delays to the Clinical Operations Lead.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;span style=\u0026quot;text-decoration: underline;\u0026quot;\u0026gt;Requirements\u0026lt;/span\u0026gt;:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in life sciences, business, or related field required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Typically 5+ years of experience in clinical operations, vendor\u0026amp;nbsp;management, or clinical trial management within biotech, pharma, or CRO\u0026amp;nbsp;environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of clinical trial processes, vendor oversight, and\u0026amp;nbsp;GCP/ICH guidelines\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience managing contracts, budgets, and vendor relationships across\u0026amp;nbsp;multiple studies or programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with CRO models, pass-through costs, and financial tracking\u0026amp;nbsp;processes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent organizational and project management skills with strong\u0026amp;nbsp;attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong communication and stakeholder management skills, with the ability\u0026amp;nbsp;to work cross-functionally\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to manage multiple priorities in a fast-paced, evolving environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with clinical systems (e.g., CTMS, eTMF) and financial tracking\u0026amp;nbsp;tools preferred\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;em\u0026gt;Compensation: The salary range for this position is $135,000 to $145,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.\u0026amp;nbsp;\u0026lt;/em\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;p\u0026gt;Epicrispr Biotechnologies is an early-stage biotechnology company developing a novel technology platform that can provide safe and persistent control of targeted gene regulation. Our proprietary platform represents an entirely new class of therapeutics that can be leveraged to treat severe disease across numerous therapeutic areas, including complex diseases impacted by multiple genes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Epicrispr Biotechnologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4049107004,"name":"ClinOps-CMC-Reg","child_ids":[],"parent_id":null}],"offices":[{"id":4027644004,"name":"Epicrispr Biotechnologies","location":"South San Francisco, California, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":6}}