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- 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- Initial Therapeutics, Inc. seeks a Sr. Director, Head of Regulatory & Medical Writing to lead regulatory documentation for submissions. This role demands extensive experience in oncology clinical research, strong leadership in regulatory writing, and exceptional communication...Suggested
- ...Francisco and Seattle-based company leading the development of adoptive T... ...We seek an experienced Regulatory professional to manage... ...with pipeline and late phase clinical development, working in partnership... ...excellent project management and writing skills, and a good...Remote work
- Senior Director, Regulatory Affairs (Strategy, Hematology Oncology) Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization... ...at the forefront of patient care, writing medicine’s next chapter with a new script...For contractors
- Nurix in Brisbane, California, is seeking a Sr. Director, Head of Regulatory & Medical Writing to lead the regulatory writing efforts for key project submissions... ...with cross-functional teams to produce clinical documents, managing internal and external writing resources...
$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...$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$220k - $270k
Senior Director / Director, CMC Regulatory Affairs 15 hours ago Be among the first 25 applicants... ...ORIC Pharmaceuticals is a clinical stage biopharmaceutical... ...is responsible for leading CMC regulatory activities... ...Excellent CMC technical writing and communications skills...Full timeCurrently hiring- BioSpace is seeking a highly motivated Senior Director, Medical Writing with extensive experience in the biotech industry. This role is responsible for leading the development of high-quality regulatory documents that support global oncology programs. The position involves...
- 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
- ...Medical Director, Drug Safety Nurix Therapeutics is a clinical stage biopharmaceutical company focused on... ...forefront of patient care, writing medicine’s next... ...clinical development, regulatory affairs, and clinical... ...as the medical safety lead for assigned products,...
$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$169.5k - $248.6k
...Purpose The purpose of the Senior Director, Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to develop and... ...issues. For preclinical and early clinical development programs, the GRL... ...including delivery device and relevant medical devices) development,...Full timeLocal areaFlexible hours$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- Vir Biotechnology, Inc. is seeking a highly motivated Director of Regulatory CMC to lead global regulatory strategy for clinical development and commercialization across multiple modalities. You will collaborate with Technical Operations and Regulatory Affairs to plan...Work at office3 days per week
$140k - $214k
...Therapeutics in Brisbane, California is looking for a Senior Manager, Regulatory CMC to drive regulatory submissions in a collaborative environment. The role involves managing CMC aspects of clinical products and ensuring regulatory compliance. Ideal candidates will have...- 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
$280k - $320k
International Executive Service Corps is seeking a Sr. Director of Medical Writing to oversee all scientific, medical, and regulatory writing activities. This role ensures full life-cycle support from clinical protocols through regulatory submissions. The ideal candidate...- US AMR-Jones Lang LaSalle Americas, Inc. seeks a Director for Health, Safety, Security & Environment in South San Francisco. The role involves managing health and safety operations, leading compliance programs, and overseeing training across a portfolio. A Bachelor's degree...
$150k - $160k
...organization's policies, California Veterinary Medical Board standards, and state laws. This... ...lectures as needed. Participate in writing educational materials and articles for the... ...organization. Participate in periodic vaccine clinics, educational programs and special events...Work at officeFlexible hours- Jones Lang LaSalle Incorporated seeks a Director, Health, Safety, Security & Environment to oversee its HSSE operations in South San Francisco... ...implementing compliance programs, managing training, and leading HSSE initiatives across sites. With a focus on safety...
$270k - $360k
...Medical Director/Senior Medical Director Tenvie Therapeutics... ...108, are in Phase 1 clinical development. TNV262 is... ...on Medical Director to lead early- and mid-stage... ...-quality clinical and regulatory documentation Lead... ...scientific and medical writing skills; able to produce...Local areaRemote work- Sutro Biopharma, located in South San Francisco, is seeking a Medical Director to lead the clinical development of antibody-drug conjugates (ADCs). The ideal candidate will have an MD or MD/PhD, with 2-5 years of experience in oncology clinical trials, particularly in early...
- Sutro Biopharma, Inc. is seeking a Medical Director to provide leadership for oncology clinical trials, particularly in antibody-drug conjugates (ADCs). The ideal candidate will possess an MD or MD/PhD, with 2-5+ years of experience in clinical trials and a strong background...
$228k - $280k
..., located in South San Francisco, is seeking a Director of Biostatistics to lead biostatistical strategy for clinical studies. The role involves overseeing all biostatistical... ...teams, and representing biostatistics in regulatory interactions. The ideal candidate has an...- 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...
- Nurix Therapeutics seeks a Sr. Director, Head of Regulatory & Medical Writing to lead regulatory writing strategy and deliverables for pivotal clinical documents. You will guide internal writers and contractors, allocate resources, and ensure high-quality submissions in...For contractors
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