Lead Medical Writing Director — Clinical & Regulatory
Enigma Search
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 ideal candidate will possess an advanced life sciences degree, with 8+ years in the field, strong communication skills, and the ability to collaborate effectively within teams. This position is vital for driving successful clinical program documentation and vendor coordination. #J-18808-Ljbffr Enigma Search
- IDEAYA Biosciences, Inc. in South San Francisco is looking for a Senior Director, Medical Writing to lead the strategy and development of clinical and regulatory documents across oncology programs. This role entails overseeing a medical writing team and managing projects...Suggested
$245k - $302k
Initial Therapeutics, Inc. is seeking a Senior Director of Medical Writing in South San Francisco. The ideal candidate will provide leadership on regulatory documents and oversee a team, requiring an extensive background in oncology and successful IND submissions. Competitive...Suggested- ...South San Francisco, CA is hiring a Director, CMC Regulatory Affairs to lead regulatory strategies for CMC... ...collaborate with regulatory, quality, clinical, and manufacturing teams to develop... ...The role requires strong scientific writing, experience with INDs/NDA/MAA filings...Suggested
- A leading biotechnology company in South San Francisco seeks a Director of Clinical Regulatory to oversee multiple clinical drug candidates and drive development as a regulatory project lead. The role involves overseeing global Health Authority interactions, leading project...Suggested
$220k - $270k
ORIC Pharmaceuticals is seeking a Senior Director/Director of CMC Regulatory Affairs to lead CMC regulatory activities in South San Francisco. The ideal candidate... ...the pharmaceutical industry and excellent technical writing skills. This role requires collaboration across...Suggested$265k - $285k
...comResponsibilities include: Provides regulatory leadership in support of... ...cross-functionally with Clinical Development, Clinical Operations, Medical Affairs, CMC, and... ...PRIME, Orphan Drug, etc.Lead and manage interactions... ...regulatory writing and review skills with demonstrated...$245k - $285k
...candidate will be responsible for leading and managing the regulatory affairs within CMC function. This... ..., CMC development and exposure to clinical regulatory strategy is highly desired... ...needs. Track and report on Medical Writing and Regulatory Operations projects...Contract work- Maze Therapeutics is seeking a Director of Medical Writing to lead the medical writing function across development programs, ensuring accuracy, consistency... ..., and submission-readiness. Reporting to the VP of Regulatory and Quality Science, you will manage internal teams and...
- Position Title: Director, Regulatory Affairs (Strategy, Immunology and Inflammation... ...) Nurix Therapeutics is a clinical stage biopharmaceutical... ...forefront of patient care, writing medicine’s next chapter with... ...serve as the global regulatory lead (GRL) for the immunology and...For contractorsWork at office
- Nurix Therapeutics, Inc. is seeking a Sr. Director, Head of Regulatory & Medical Writing to lead the regulatory writing group and guide the preparation of high-quality regulatory documents for clinical trials and submissions. You will collaborate with Clinical Science,...
- Maze Therapeutics is seeking a senior regulatory medical writer to lead the function across development programs. You will develop high-quality clinical and regulatory documents and manage external vendors to ensure timely, compliant deliverables. You will partner with...
$198.6k
...The PositionThe Sr. Medical Science Director/Sr. Medical Director... ...strategy and relevant clinical and payer issues, while... ...the ability to lead fit-for-purpose teams... ...meaningful perspective for regulatory and other scientific... ...clinical relevance, medical writing and reviewing,...Full timeLocal areaShift work$299k - $349k
...biopharmaceutical company in California is seeking a Senior Medical Director to lead late-stage clinical development programs in Oncology. This role requires... ...collaboration with cross-functional teams to ensure regulatory compliance. The pay range is between $299K and $349K...- ORIC Pharmaceuticals is a clinical stage biopharmaceutical company... ...Officer, we are hiring a Director, CMC Regulatory Affairs to join our... ...Operations team. This role leads CMC regulatory activities and... .... Excellent CMC technical writing and communication skills with...
- IDEAYA Biosciences is hiring a Senior Director of Medical Writing in South San Francisco to lead the development of clinical and regulatory documents in oncology. The role is pivotal for both early and late-stage programs and requires strong leadership skills, deep expertise...
- Maze Therapeutics is seeking a Director of Medical Writing to lead the medical writing function across clinical programs, ensuring documents are accurate, consistent, and submission-ready. Reporting to the VP of Regulatory and Quality Science, you will partner with Regulatory...
$254.13k - $289.39k
...Therapeutics is a clinical stage biopharmaceutical... ...of patient care, writing medicine’s next... ...responsible for providing regulatory writing expertise... .... The Sr. Director, Head of Regulatory & Medical Writing will be responsible... ...effectively and lead in cross-functional...Odd jobFor contractorsFlexible hoursShift work- A leading life sciences company in South San Francisco is seeking a Director of Clinical Quality Assurance to ensure compliance with FDA regulations and oversee GCP QA programs. The ideal candidate will have extensive experience in clinical quality assurance and expertise...
$302.01k - $390.83k
...OVERVIEW:The Executive Director, Head of Precision Medicine Regulatory is responsible for defining and leading enterprise-wide... ...validation of biomarkers in clinical studies. You will... ...communication and writing skills, project... ...company-sponsored medical, dental, vision,...Full timeFor contractorsWork at officeLocal areaFlexible hours$211k - $258.67k
Neurodegenerative diseases are one of the largest medical challenges of our time. Denali... ...Denali is founded on the collaboration of leading scientists, industry experts, and... ...Responsibilities Developing and implementing regulatory strategy for complex development...Remote jobTemporary workWork experience placementLocal area$270k - $360k
...Medical Director/Senior Medical Director, Clinical Development TenvieTherapeutics is developing precision... ...‑on Medical Director to lead early‑ and mid‑stage... ...‑quality clinical and regulatory documentation Lead or oversee... ...scientific and medical writing skills; able to produce...Local areaRemote work- ...possible, together.Job DescriptionFUNCTION: Regulatory Affairs Business Operations - RA Human... ...indirect reports, with responsibility to lead other people managers. You will routinely... ...package. Benefits include company-sponsored medical, dental, vision, and life insurance plans...Full timeFor contractorsLocal areaWorldwide
$244k - $305k
Revolution Medicines is a late-stage clinical oncology company developing novel... .... The Opportunity: The Senior Director, Molecule Global Regulatory Lead will develop and execute global... ...closely with Regulatory Operations, Medical Writing, Clinical Development, Biometrics...Full timeLocal area- Veratherapeuticsinc seeks a Senior Manager, Regulatory CMC to manage regulatory submissions and... ...skills, and the ability to lead cross-functional projects. Candidates should... ...bonuses, equity options, and comprehensive medical benefits. #J-18808-Ljbffr Veratherapeuticsinc
- Genentech is seeking a transformational Director, Environment to lead environmental excellence at the South San Francisco campus. You will oversee... ...to site leadership, aligning with Roche policies and regulatory expectations. The role requires 12+ years of progressive...
$211k - $264k
...Revolution Medicines is a late-stage clinical oncology company developing novel... ...pathway. The Opportunity The Director of Regulatory Affairs (Global Filing Lead) is accountable for driving... ...age, disability, marital status, medical condition, and veteran status. Revolution...Full timeWork experience placementLocal area$198k - $257k
...secured partnerships with leading global biopharmaceutical companies... ...partner for global clinical development. Our unique business... ...Function: The Associate Director, Regulatory Affairs supports the... ..., Nonclinical, Biometrics, Medical Writing, CMC, and other functions....Full timeWork at officeWorldwideRelocation package- ...Iovance Biotherapeutics, Inc. is seeking a Director of Regulatory CMC to lead one or more drug development programs... ...The role requires deep understanding of clinical development strategies for oncology products and expert writing of regulatory documents. The candidate will...
- ...platform has demonstrated promising clinical data across multiple solid tumors... ...with cancer. Overview The Director, Regulatory CMC, is responsible for leading one or more drug development programs... ...content, organization, clarity of writing, and accuracy. Leads cross-...Work at officeRemote work
$210k - $240k
...break down the alcohol byproduct that leads to rough mornings after drinking. In 2... ...Ventures, among others. About the Role As Director of Regulatory Affairs , you will own and execute... ...policy experience. Excellent technical writing and oral advocacy skills, including...Work at officeLocal areaHome officeFlexible hoursDay shift
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