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In this role, you will provide critical analytical support for their portfolio of experimental drugs, collaborating closely with various functional areas including clinical operations, clinical science, biometrics, and external partners.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Represent and provide clinical pharmacology expertise and leadership at cross-functional development project team, clinical subteam, study team, partnering with clinical research, biometrics, project management, clinical operations, drug metabolism, biology/biomarkers, toxicology etc.
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Knowledge of and experience in selling biometrics, regulatory submissions, and regulatory operations will be a distinct advantage. 5+ years of related experience, including 3 years of relevant industry experience, preferably in data services (data management and biometrics) or a clinical research environment.
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This is a ground floor opportunity to help to build the statistical programming function within the Biometrics department. The Associate Director statistical programming leads the programming activities for multiple clinical development programs by providing strategic and hands-on input in a cross-functional setting using both internal and external resources.
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As the Associate Director, Clinical Quality Assurance (CQA), you are a key member of the Clinical Quality team maintaining representing Clinical QA in cross functional setting, and advising Cytokinetics Clinical Operations, Biometrics, Drug Safety and Pharmacovigilance teams on GCP matters.
$185,000 - $226,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Routinely provide updates regarding study status to senior management and responsible for ensuring that study management teams are led collaboratively and productively with representatives from clinical research, finance, regulatory affairs, project management, drug safety, biometrics, manufacturing and legal.
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Networking and Alliance Building: Capacity to work across many interfaces and line functions: clinical development, research, biometrics, computational biology, regulatory, operations, data management, commercial, med affairs and project management.
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Work with key cross-functional stakeholders to manage the content of all documents including, but not limited to: Clinical Development, Drug Safety, Pharmacovigilance, Regulatory, Clinical Operations, Data Management, Biometrics, Clinical Pharmacology, CMC/Manufacturing, Legal, Investor Relations, and Corporate Strategy.
$240,000 - $275,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work with statisticians/biometrics to develop the required tables/listings/figures and contribute to the interpretation of efficacy and safety data from clinical trials. Title: Contract Director/Sr. Director, Clinical Science (Early Oncology Development.
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Reporting to the Head of Biometrics, the Director of Biostatistics will support oncology drug development, providing statistical leadership and oversight to the development plans, regulatory interactions, and commercial evaluation of investigational compounds in one or more indications.
$190,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Collaborate with interdisciplinary teams including biometrics, data management, IT, data science teams to implement Vir's enterprise data architecture, structure, systems, and analytics. Vir Biotechnology is seeking a Senior Director to develop and execute our Translational and Clinical Development roadmap integrating Data Science and real-world data (RWD) into innovative clinical development plans, study designs, and integrative data analysis across our clinical development portfolio.
$164Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The role will partner with multiple internal groups including Clinical, Regulatory Affairs, Biometrics, Medical Safety, and Non-Clinical to ensure high quality and on-time deliverables that meet regulatory standards.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Reporting to the VP of Biometrics, you will support both early and late phase oncology products, interact with regulatory officials on all statistical related matters, oversee development plans, and provide strategies for clinical study design, endpoint selection, sample size calculations, statistical analysis plans (SAP) and more.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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The Director of BSO is an experienced project and matrix leader who is responsible for managing the analysis and reporting activities for drug development projects sponsored by Teva Research and Development (R&D.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Ensures that proper processes are adhered to regarding the initiation, conduct, and closeout of all globally- run studies as well as the maintenance of the Trial Master File for such trials; responsible for ensuring regulatory compliance and together with Biometrics, delivery of high-quality data.
ExpandApply NowActive JobUpdated 19 days ago
biometrics director jobs in South San Francisco, CA
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