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📑 Senior Director, Regulatory Affairs*Bay Area- Hybrid*Meet has partnered with a fantastic Bay Area pharma focused in treatments for metabolic, psychiatric, and oncologic disorders. Our client has an approved product and a dynamic late-stage pipeline. You will be coming in to lead their Oncology portfolio and you' ...
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📑 Associate Director/Director, Regulatory Affairs (Oncology)Remote - East Coast CandidatesMeet has partnered with a very well-established pharma with roughly 20 approved products and a robust development pipeline. They are looking for an Associate Director or Director of Regulatory Strategy to join their team. Thi ...
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📑 We are partnered exclusively with an exciting biotech company who are looking to bring on their first hire within their regulatory affairs department. Role can be at Director or Senior Director level.The team are looking for individuals with the following experience:Authoring and submitting an IND (the company i ...
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📑 Director, Regulatory Affairs CMCW2 ContractSalary Range: $249,600 - $270,400 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:This position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development a ...
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📑 Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Hybrid position - will work partly in office and partly remote. Looking for a Regulatory Affairs Specialist with at least 2 years of regulatory experience along with submissions. Will work on IND submissions (publ ...
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📑 Director, Regulatory Affairs CMCW2 ContractSalary Range: $249,600 - $270,400 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:This position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development a ...
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📑 I am partnered with a Small growing biotechnology company in the San Francisco area that is looking for a Pharmacokinetics expert to join their team! In this position you would be given the opportunity to be the first Pharmacokinetics expert and begin to build out the team along the way. My client is looking for ...
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📑 Clinical Development Leader (Medical Director to Senior Director level)San Francisco (remote/hybrid) **MUST reside on the West Coast or willing to relocate**Full-timeSciPro is working with one of the most exciting names in Oncology. This position holds high visability and will report directly to the CMO.My clien ...
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📑 A California-based biopharmaceutical company is looking to add an experienced professional to their CMC Quality Control Department as a Writer / Reviewer. In this role, the CMC Quality Control Writer / Reviewer will be responsible for authoring, drafting. reviewing, and approving the Regulatory QC CMC sections o ...
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📑 Director, CMC Regulatory AffairsDirect Hire Fulltime RoleSalary Range: $208,000 - $235,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:The position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical ...
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📑 Team Lead, INSC Central Flow, INSC Central Flow, INSC Central Flow 2023 / IND, Team Lead, INSC Central Flow, INSC Central Flow, INSC Central Flow Graduate as per norms BASIC QUALIFICATIONS - Speak, write, and read fluently in English - Experience with Microsoft Office products and applications PREFERRE ...
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📑 This is an opportunity to work with an innovative biotechnology company working on the development and manufacturing of small molecules for a diverse portfolio of therapeutic targets. To support the continued growth of the pipeline, we are looking for an experienced Senior/Executive Director of CMC to guide stra ...
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📑 Title: Java with Cassandra Location: Jersey City, NJ Type: Contract W2 Job Description: 'Java developer with experience developing solutions/API and having a working knowledge of Cassandra and Kafka. Essential Skills -Java, Spring, Cassandra, Kafka, API. ...
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📑 Director, Clinical Development - Immunology*Remote for East Coast Candidates*Meet has partnered with a well-established pharma based on the East Coast! They are looking for a Director of Clinical Development to join their immunology department. This position will be reporting into a Senior MD and will be support ...
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📑 Associate Director, Regulatory AffairsThis position will serve as the company US Agent and a contact point between the FDA and company sites. Responsible to communicate with FDA for all regulatory issues/questions and provide regulatory guidance to internal constituents. It will lead a team of Regulatory Associa ...
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📑 A clinical-stage biotechnology company based in San Francisco, backed by Third Rock Ventures, is harnessing the power of adipocyte biology and the latest advances in human genetics to develop first-in-class, next-generation medicines for cardiometabolic diseases. The company is building a pipeline of therapies t ...
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📑 RBW is partnering with an innovative clinical-stage, Biotech in their search for a newly created position - (Sr.) Director, R&D Quality Assurance. Our client is focused on discovering and developing medicines for the treatment of Crohn's and other inflammatory diseases.The candidate will report directly to the H ...
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📑 About Firefly Bio:Firefly Bio is a Bay Area venture-backed company. Our mission is to unlock the full potential of bioconjugates and develop medicines with long-lasting benefits for patients. We are establishing an expert team to build state-of-the-art platform capabilities for the invention and development of i ...
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📑 A clinical-stage biotech focused on Rare Diseases. This company utilizes antibodies to harness the bodies immune system to fight off disease.The RoleThis person ill serve as the GRL for the company's early stage proprietary pipeline as well as supporting partnered programs with large pharma , reporting into the ...
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📑 About Firefly Bio:Firefly Bio is a Bay Area venture-backed company. Our mission is to unlock the full potential of bioconjugates and develop medicines with long-lasting benefits for patients. We are establishing an expert team to build state-of-the-art platform capabilities for the invention and development of i ...
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📑 Our clinical-stage biopharmaceutical client is seeking a Medical Director / Senior Medical Director with strong Oncology Clinical Development experience to cover development programs spanning phases I,II,III.Responsibilities:clinical leadership; from early-stage clinical trial design for novel cancer drugs throu ...
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