Senior Medical Writing Lead for Clinical & Regulatory
Calico 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 at a biotech or pharmaceutical company. Responsibilities include document leadership, vendor management, and process improvement. A strong understanding of regulatory requirements and excellent communication skills are essential. The estimated salary range is $230,000 - $240,000 with additional bonuses. #J-18808-Ljbffr Calico Life Sciences
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...biopharmaceutical company in California is seeking a Senior Medical Director to lead late-stage clinical development programs in Oncology. This role... ...collaboration with cross-functional teams to ensure regulatory compliance. The pay range is between $299K and $349...SeniorMedicalRegulatory- ...Job Title: Senior Clinical Scientist Location: San Francisco... ...address critical unmet medical needs. We're looking... ...Science, Data Science, Regulatory and Quality teams, to... ...intraoperative FIH study. Lead study strategy,... ...Excellent scientific writing, critical-thinking, and...SeniorMedicalRegulatoryFull timeFlexible hours
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...peptide drugs. We are advancing a clinical‐stage pipeline of... ...program goals.Supports the Study Lead as an integral member of a multifunctional... ...amendments, and works with medical writing to initiate protocol... ...and study drug, safety, regulatory, and legal questions....SeniorMedicalRegulatoryContract workWork at officeRemote work- Structure Therapeutics is seeking a highly motivated Sr. Clinical Trial Manager (SCTM) to join our Clinical Operations team in California... ...SCTM collaborates with teams in the US and Shanghai, supports regulatory readiness, and ensures SOP compliance. #J-18808-Ljbffr...SeniorRegulatory
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- Corvus Pharmaceuticals is a clinical-stage biopharmaceutical company seeking a regulatory-minded clinician for hands-on support of clinical plans, protocols and regulatory... ...with the VP, Clinical Development and act as a Medical Monitor, coordinating data reviews and study...SeniorMedicalRegulatory
$261k - $304.5k
## Senior Director, CMC Lead Product DevelopmentApplylocations: South San Francisco... ...program(s) across the clinical development life-cycle and... ...supply chain, CMC, quality, regulatory, program & portfolio management... ...possess good scientific writing skills and good verbal skills...SeniorRegulatory
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