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Minimum of 10 years of experience in Clinical Regulatory Affairs within drug development. This pivotal role will spearhead regulatory strategies and activities concerning the development and approval of cell therapy products.
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MBA with 15 years of experience in Corporate Strategy, Corporate Development, M&A integration, or related areas within the pharmaceutical or biotechnology industry (a combination of experience and education may be considered.
$329,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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MD (nephrologist preferred) in a drug development-related discipline with 11+ years of experience in the pharmaceutical or biotechnology industry, with direct experience in drug development and 5+ years of leadership experience.
$390,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Interact with external authors and internal collaborators within Global/Regional Medical Affairs, Clinical Development, and Drug Discovery organizations to develop and review publication content.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Responsible for oversight of the outsourced analytical development activities associated with the development, validation, technology transfer, and line extension of drug product.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Expert knowledge of drug development strategies for various modalities including small molecules, biologics, therapeutic peptides, therapeutic areas (including neuroscience and endocrineology) and regulatory regions including US, Canada, Europe and Japan.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Work collaboratively with Pharmaceutical Science for drug substance and drug product development, GMP Quality Assurance, in addition to Project Management, Clinical Operations, Clinical Supply, and Regulatory Operations.
$235,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Develop bioanalytical methods using HPLC and mass spectrometry (e.g., LC/MS/MS) methods to support discovery activities related to small molecule therapeutics, including PK and drug metabolism to identify structure activity- and structure-property- relationships to assist in further structural optimization.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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As the Senior Vice President, Chief Medical Officer (SVP/CMO), reporting to the Chief Executive Officer, you will serve as the lead medical voice for Halozyme providing leadership and guidance in the areas of Subcutaneous Drug Development with ENHANZE and Auto-Injectors, Regulatory Affairs, Drug Safety & Medical.
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Genesis originated in graph machine learning research in Vijay Pande’s lab at Stanford, when it was joined by legendary drug hunters and biotech entrepreneurs (including Dr. Leonard Bell, founder and CEO of Alexion Pharmaceuticals, acquired by Astra Zeneca for $39Bn; and Peppi Prasit, storied chemist from Merck known for Vioxx, Arcoxia, Singulair, who then went on to found Amira Pharmaceuticals, acquired by BMS, and Inception Sciences.
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Additionally, the role involves collaboration with cross-functional teams, including Medicinal Chemistry, Biology, and Pharmacology, to integrate radiochemistry efforts into broader drug discovery initiatives.
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The Senior Manager/Associate Director of Drug Safety & Pharmacovigilance (PV) Quality, is a key role and is responsible for oversight of Drug Safety & PV quality, compliance, and alliance management activities, thus always promoting inspection readiness and maintaining a robust global compliance program within the Quality Assurance department.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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In-depth, working knowledge of the drug development process and ICH requirements related to CMC activities in support of IND and BLA registration. Increasing responsibility in a quality, analytical development, process development, regulatory, or manufacturing environment.
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Sr. Manager, Drug Safety & Pharmacovigilance Quality Assurance Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are a fully integrated contract development and manufacturing organization with sites in Belgium, United States, Japan, and India providing comprehensive development, cGMP manufacturing, and aseptic fill finish services.
$46.5 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago
drug development jobs in San Diego, CA
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