Senior Medical Writing Lead: Clinical & Regulatory Strategy
Meet Life Sciences
Meet Life Sciences is seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory documents in support of complex drug development programs. This role shapes document strategy, ensures scientific accuracy, and drives cross-functional alignment across clinical, regulatory, and biostatistics teams. Based in the San Francisco Bay Area with hybrid work, relocation package is available for this leadership position. #J-18808-Ljbffr Meet Life Sciences
- A biotech research company in South San Francisco seeks an Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory documents. The ideal candidate must possess a Master's degree and over 8 years of experience in scientific writing...SeniorMedicalRegulatory
- Trebla Talent is seeking a Sr./Medical Director to lead clinical strategy and execution for a cutting-edge biotech in San Francisco. The role will require... ...trial design, interpret data for publications and regulatory submissions, and represent the company in dialogues with...SeniorMedicalRegulatory
$346k - $397k
...is a late‑stage clinical oncology company... ...developer to serve as Senior Medical Director of... ...critical role you will lead the clinical... ...Development Plan (CDP) strategy, drive the... ...with scientific, regulatory, and commercial teams... ...design, protocol writing, CRF construction...SeniorMedicalRegulatory- Cynosure Staffing in California is seeking an Associate Director, Medical Writing to lead and oversee the creation and review of high-quality clinical and regulatory documents in compliance with ICH and global guidelines. The role emphasizes project leadership, cross-functional...SeniorMedicalRegulatory
- ...Senior Clinical Scientist Job Title: Senior Clinical... ...address critical unmet medical needs. We're looking... ..., Data Science, Regulatory and Quality teams, to... ...intraoperative FIH study. Lead study strategy, protocol... ...Excellent scientific writing, critical-thinking,...SeniorMedicalRegulatoryFull timeFlexible hours
- Enigma Search is looking for an Associate Director, Medical Writing, to oversee the development of clinical and regulatory documentation. The ideal candidate will have an advanced degree in life sciences and over 8 years of medical writing experience in biotech or pharmaceutical...SeniorMedicalRegulatory
$186k - $235k
Structure Therapeutics in South San Francisco seeks an Associate Director of Medical Writing. The role includes leading the development of regulatory documents and performing quality control reviews to ensure compliance. The ideal candidate will have over 5 years of experience...SeniorMedicalRegulatory- ...Therapeutics is seeking a Sr. Director, Head of Regulatory & Medical Writing to lead the medical writing group and shape the strategy for key regulatory documents. You will... ...quality deliverables, and collaborate with Clinical Science and Regulatory teams across oncology...SeniorMedicalRegulatoryContract work
$270k - $360k
...Medical Director/Senior Medical Director, Clinical Development Tenvie Therapeutics... ...Medical Director to lead early- and mid-stage... ..., and support regulatory submissions partnering... ..., and biomarker strategies Provide ongoing... ...scientific and medical writing skills; able to...SeniorMedicalRegulatoryFull timeLocal areaRemote work- Insightec is a growing medical technology company... ...for independently leading the clinical trial study team and... ...trials, to include regulatory compliance, high quality... ...with regulatory writing, strategy development, and corrective... ...study teams, senior management, and at Clinical...SeniorMedicalRegulatoryContract workTemporary workLocal areaFlexible hours
$125k - $180k
...Clinical Scientist/Senior Clinical Scientist Tenvie... ...Translational Science, and Regulatory to ensure high‑... ...: Lead development of core... ...training material, medical monitoring plans... ...to clinical strategy and study design... ...Excellent scientific writing skills with a...SeniorMedicalRegulatoryFull timeLocal areaRemote work- Kardigan in Princeton, NJ is seeking a Senior Director, Clinical Pharmacology to lead strategies across cardiovascular development and regulatory interactions with FDA and global... ...Biometrics, Regulatory Affairs, and Medical Writing to ensure successful submissions and...SeniorMedicalRegulatory
- Erasca is seeking a Senior or Executive Director, Clinical Development to drive late-stage... ...role reports to the Chief Medical Officer and collaborates with... ...to develop innovative strategies and ensure successful trial execution and regulatory submissions. The position...SeniorMedicalRegulatory
$244k - $305k
...is a late-stage clinical oncology... ...developer to serve as Senior Director,... ...studies including regulatory submissions. You... ...vital role in leading the clinical science... ...Plan (CDP) strategy, driving the development... ...the conduct of medical/safety data... ..., protocol writing/ICF (writing or...SeniorMedicalRegulatoryFull timeLocal area- ...Central Reading Centers, Labs, Medical Coders). Author key... ...audit-ready manner. Support Lead Clinical Programmers in developing and... ...Managers, Programming, and Regulatory teams. Review study protocols... ...documentation skills, with experience writing Data Management Plans, Data...SeniorMedicalRegulatory
- ...seeking a System Director of Clinical Documentation Integrity (CDI) to lead best practices ensuring... ...The role partners with Medical Directors and HIM to... ...with quality goals. This senior position spans academic,... ...requiring strategic vision, regulatory knowledge, and strong...MedicalRegulatory
- ...Pharmaceuticals Inc. is seeking a senior leader to integrate translational medicine, clinical pharmacology, and biomarker strategy across its portfolio.... ..., reporting to the Chief Medical Officer. The role... ...through development and regulatory submissions, with a focus...SeniorMedicalRegulatory
$125k - $180k
...Clinical Development Scientist/Senior Clinical Development Scientist... ...Translational Science, and Regulatory to ensure high‑... ...to clinical strategy and study... ...prioritization Lead or co‑lead the... ...in ongoing medical and scientific... ...Excellent scientific writing skills with a...SeniorMedicalRegulatoryInterim roleLocal areaRemote work- ...and no longer the leading cause of death in the... ...Development, the Senior Director, Clinical Pharmacology will provide... ...pharmacology strategies from early through... ...development, supporting regulatory submissions, and... ...Regulatory Affairs, Medical Writing, CMC, Research, and...SeniorMedicalRegulatory
- ...San Francisco, CA, seeks a Senior Director, Clinical Science - Hematology to lead strategic Clinical Science... ...will shape disease area strategy, standardize scientific approaches... ...with Clinical Operations, Regulatory Affairs, Biostatistics, and Medical Affairs, and travel up to...SeniorMedicalRegulatory
- Genentech in San Francisco, CA seeks a Senior Principal Scientist to lead the bioanalytical strategy for our Cell Therapy portfolio. You will define... ..., Research, Translational Medicine, Clinical Development, CMC, Regulatory, and Computational Sciences to address key...SeniorRegulatory
$121k - $185k
...and compliance story. As our Senior GRC Security Lead, you will be the architect... ...aligned with evolving regulatory requirements, industry frameworks... ...policy and standards writing ability - capable of translating... ...Gongsters a variety of medical, dental, and vision plans,...SeniorMedicalRegulatoryRemote workWork from homeFlexible hours$215k - $230k
...Biosciences is a leading clinical-stage CRISPR genome... .... Summary The Senior Clinical Research... ...contribute to clinical strategy, driving the... ..., and support regulatory submissions. Responsibilities... ...scientific writing and communication... ...Excellent medical, dental, and vision...SeniorMedicalRegulatoryLocal areaRemote work$360k - $420k
...degraders to the clinic. Lycia is headquartered... ...in providing medical leadership and expertise... ...Responsibilities Lead the development,... ...and/or regulatory approval. Provide... ...Contribute to the pipeline strategy, including input... ...). Experience in writing clinical sections...SeniorMedicalRegulatoryContract workFlexible hours$260k - $275k
...Reporting to the VP, Clinical Operations, the Senior Director, Clinical... ...decision milestones and regulatory requirements. The... ...Biostatistics, and Medical Directors, to support... ...still be involved in writing DMPs (Data... ...establishing long‑term data strategy and infrastructure....SeniorMedicalRegulatoryTemporary workWork at officeLocal area2 days per week3 days per week- Med Clinic X in the United States seeks a visionary Chief Medical Information Officer (CMIO) to align clinical workflows... ...-edge health IT. You will lead clinical informatics strategy across our healthcare SaaS... ...patient safety and regulatory compliance. You will partner...MedicalRegulatory
- Enigma Search is looking for an Associate Director, Medical Writing in South San Francisco, California. This role involves leading the development of clinical and regulatory documentation, ensuring compliance with global standards, and managing the writing process. The...MedicalRegulatory
- Position: Sr./Medical Director, Clinical Development Reports To: SVP, Clinical... ...a Physician (MD) to help lead clinical strategy and execution. The Sr./... ...Strategy - Partner with senior leadership to shape clinical... ..., presentations, and regulatory documents. Collaborate Cross...SeniorMedicalRegulatory
$117k - $184.2k
...Early Clinical Scientist (ECS) coordinates the design, planning, and... .... Applies GCP, ICH, and regulatory requirements. Represents Early... ...promotes best practices. Technical writing: Co-authors protocols,... ...execution; site training/monitoring; medical/regulatory writing). Required...SeniorMedicalRegulatory$230k - $300k
...diseases with high unmet medical need. Our pipeline... ...first‑in‑class clinical asset and... ...autoimmune disease.Our lead asset is being developed... ...a Director or Senior Director of... ...clinical pharmacology strategy and execution across... ...medicine, regulatory strategy, and clinical...SeniorMedicalRegulatoryContract work
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