Head of Regulatory & Medical Writing - Oncology
BioSpace
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 alignment with timelines. Applicants should have 15+ years in oncology clinical research or regulatory medical writing, with proven leadership of writing teams and experience with NDA/BLA/MAA submissions. #J-18808-Ljbffr BioSpace
- BioSpace is seeking a highly motivated Senior Director, Medical Writing with extensive experience in the biotech industry.... ...for leading the development of high-quality regulatory documents that support global oncology programs. The position involves oversight of a medical...Medical
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...forefront of patient care, writing medicine’s next chapter... ...responsible for providing regulatory writing expertise and leadership... .... The Sr. Director, Head of Regulatory & Medical Writing will be responsible... ...0+ years of experience in oncology clinical research experience...MedicalOdd jobFor contractorsFlexible hoursShift work- 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...Medical
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...Description Erasca is a clinical-stage precision oncology company focused on discovering,... ...to the Executive Director, CMC Regulatory Affairs, the Senior Manager or Associate... ...Paid Time Off, Holiday, and Sick Leave, Medical, Dental and Vision Plans, Short- and Long...MedicalTemporary workCasual workLocal areaWorldwideFlexible hours- 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...Medical
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Revolution Medicines is a late-stage clinical oncology company developing novel targeted... ...programs. Oversee the development of global regulatory therapeutic area and product strategies... ..., age, disability, marital status, medical condition, and veteran status. #J-18808...MedicalWork experience placement$164k - $205k
Revolution Medicines is a late‑stage clinical oncology company developing novel targeted... ...providing hands‑on support to Commercial and Medical field teams during product... ...refreshers based on emerging risks and regulatory changes. Delivers live, in‑person and virtual...MedicalFull timeLive inLocal area- ...serious health issues today and address the medical challenges of tomorrow. We strive to... ...therapeutic areas including immunology, oncology and neuroscience - and products and services... .... We are currently seeking a Regulatory Affairs Director to join our growing regulatory...MedicalFull timeLocal area
- ...serious health issues today and address the medical challenges of tomorrow. We strive to... ...therapeutic areas including immunology, oncology and neuroscience - and products and services... ...: Provide global oversight of EHS regulatory compliance. Own the Global EHS...MedicalFull timeTemporary workLocal area
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...Revolution Medicines is a late‑stage clinical oncology company developing novel targeted... ...strategic and hands‑on Associate Director, CMC Regulatory who will be responsible for executing... ..., age, disability, marital status, medical condition, and veteran status. Revolution...MedicalWork experience placement$211k - $264k
...Revolution Medicines is a late-stage clinical oncology company developing novel targeted... ...pathway. The Opportunity The Director of Regulatory Affairs (Global Filing Lead) is... ...ancestry, age, disability, marital status, medical condition, and veteran status. Revolution...MedicalFull timeWork experience placementLocal area- ...and individual study protocols Writes or assists in writing of... ...Investigator Brochures, DSURs and other regulatory documents Assist other team... ...conduct of trial Assist in Medical Monitor responsibilities Work... ...years of biotech experience (oncology, dermatology or autoimmune...MedicalWork at officeImmediate start
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ORIC Pharmaceuticals Inc. is seeking a Director, Medical Affairs, based in South San Francisco. The successful candidate will develop and execute strategies for oncology therapies including rinzimetostat and enozertinib, working collaboratively across various functions...Medical$244k - $305k
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...Compliance Counsel Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology... ...organization’s commitment to ethical business practices, and regulatory compliance as we prepare for our first potential commercial...MedicalWork experience placementWork at officeLocal areaFlexible hours3 days per week$220k - $275k
ORIC Pharmaceuticals, Inc. is seeking a Director of Medical Affairs for their South San Francisco office. The successful candidate will drive the Global Medical Affairs strategy for key oncology therapies. Ideal candidates should have over 8 years of experience in medical...MedicalWork at office- ...serious health issues today and address the medical challenges of tomorrow. We strive to... ...therapeutic areas including immunology, oncology and neuroscience – and products and services... .... Extensive knowledge of the global regulatory, HTA and PR&A landscape, as well as...MedicalFull timeWork experience placementLocal area
$275k - $280k
...drug‑development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs. Position Description The Director of Regulatory CMC will lead the development and execution of global CMC regulatory strategies for our pipeline of...Medical- ...Position Title: Director, Regulatory Affairs (Strategy, Immunology and Inflammation) Nurix Therapeutics... ...at the forefront of patient care, writing medicine’s next chapter with a new script... ...in close collaboration with the SVP, Head of Regulatory Affairs and the development...For contractorsWork at office
- ...information at Job Purpose / Summary We seek an experienced Regulatory professional to manage regulatory activities associated with pipeline... ...-functional interactions, excellent project management and writing skills, and a good understanding of the underlying science....Remote work
- Senior Director, Regulatory Affairs (Strategy, Hematology Oncology) Brisbane, California, United States Job Summary Nurix Therapeutics, Inc. is seeking a Senior Director Regulatory Affairs (Strategy, Hematology Oncology) to join the Regulatory team. The successful candidate...For contractors
- Nurix Therapeutics, Inc. is looking for a Senior Director of Regulatory Affairs in Brisbane, California. The candidate will guide and execute regulatory strategies, ensuring compliance and quality in nonclinical and clinical submissions. With over 12 years of experience...
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...advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases. Position Summary Vera is seeking a Senior Manager, Regulatory CMC to join an experienced, fast‑paced and collaborative team. The...Medical$190k - $275k
...enterprises. Working closely with the head of security and compliance,... ...to detail, excellent writing skills, and who wants to build... ...and ensure new features meet regulatory standards Establish vendor risk... ...25 days of statutory leave) Medical, Dental, and Vision benefits...MedicalFull timeFor contractorsWork at officeLocal area
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