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Experience in drug development is a plus. Key Responsibilities Support integrated evidence planning in early phase development (development of playbook (IEP execution team), training (IEP development & refresh.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Strong knowledge of NMR including application in the pharmaceutical industry, establishing new NMR methods, and prospectively impacting problems related to drug discovery, characterization, and development.
$239,200 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Research and Early Development (gRED) is seeking a highly motivated, scientifically curious, skilled, and productive research associate to advance efforts on drug discovery and gene therapy modalities in a contract role.
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Support development of regulated and clinical bioanalytical strategies for large molecule drug candidates, and conduct PK, ADA, and biomarker assays internally. Perform quantitative bioanalytical immunoassay experiments to support non-regulated pharmacokinetic (PK) analyses of biotherapeutic drug candidates and evaluate anti-drug antibody (ADA) response.
$153,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Reporting to the Vice President, CMC Operations, the Head of/Senior Director CMC Operations (Drug Substance) will manage activities related to Process Development, Tech Transfer and Manufacturing of Drug substance.
$280,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Our Client's global life sciences practice, one of the largest in the U.S., is seeking a regulatory counsel with at least 10+ years of industry experience in drug/biologics development to join our FDA regulatory group.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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As a Pharmacokinetics/Clinical Pharmacology Principal Scientist, you will utilize your experience to further characterize the novel kinetics of our new therapeutic modality and build complex models that inform study designs and decision-making throughout the drug development process.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provide leadership focusing on platform innovation and preclinical program development that leads to successful FDA IND application(s) for gene therapy drug candidates. Projects requiring pharmacology support may span from platform development, target validation, preclinical development, to translational biology.
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The Gene Therapy group at SonoThera is seeking to hire a Research Scientist to become an integral part of the gene therapy drug development effort. The Gene Therapy group at SonoThera uses a collaborative, interdisciplinary, and forward-thinking approach to solving many of the current challenges facing genetic medicine discovery and drug development.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Regulatory AffairsOur Client's global life sciences practice, one of the largest in the U.S., is seeking a regulatory counsel with at least 10+ years of industry experience in drug/biologics development to join our FDA regulatory group.
$435,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Deliver impactful outcomes by leveraging a deep understanding and experience in navigating typical workflows within drug discovery, drug development, gene-to-antibody, and proteomics.
$145,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Requires a minimal of 5+ years in genomics, synthetic biology, or drug development. This individual will be responsible for driving product and application-based messaging across Twist’s business units, including core initiatives toward cancer research, drug discovery, and human genetics.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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You will represent your work at functional area meetings and provide support for purification development, analytical development, formulation and drug product teams, process analytics, manufacturing sciences, and other CMC functions.
$122,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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The successful candidate will lead analytical development and quality control for Altos AAV Gene Therapy programs. ResponsibilitiesLead analytical development and quality control for AAV gene therapy programsBuild a high performing team and establish internal and external analytical and QC capabilitiesManage contract manufacturing organizations and contract testing organizations to develop and qualify analytical testing methods, perform release and stability testing, and in-process testingEstablish product specifications to ensure product quality.
$392,150 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Transportation (TSA) Security Clearance: Candidates for employment with the San Francisco Airport Commission are required to undergo a criminal history record check, including FBI fingerprints, and Security Threat Assessment to determine eligibility for security clearance and may be required to undergo drug/alcohol screening.
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drug development jobs in South San Francisco, CA
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