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The ideal candidate will have substantial experience representing biotechs and big pharmas in licensing patents, collaborating on novel therapeutics, vaccines, diagnostic, and digital health technologies, and navigating through clinical trials toward FDA regulatory approval.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The Clinical Trial Assistant (CTA) is responsible for the support of the study team by creating, distributing, maintaining, and organizing study materials, tools and documents to ensure conduct of clinical trials is in compliance with protocol requirements, SOPs and ICH GCP Guidelines.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Partnering with key internal stakeholders and business unit teams to build dynamic communication plans for key company clinical trials, real-world evidence, and other relevant clinical/preclinical studies to deliver clear, effective, and aligned communications across multiple channels to various audiences.
$285,900 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Biorepository, Histotechnologist I is responsible for performing histology services and operational activities in support of clinical trials, research & development requests, process improvement studies, and other tissue-focused initiatives that fall outside the scope of the commercial laboratory space.
$106,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are seeking a Medical Director that is highly motivated to join our team and work on-site at an exciting biotech company based in Redwood City. The primary role of the Medical Director will be to lead and execute early- and late-stage clinical trials in type 1 and type 2 diabetes.
$310,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Ensure clinical trials are managed and executed in accordance with ICH GCP, regulations, the protocol, and company-specific SOPs. 6+ years of clinical research experience, with at least 2 years' experience in planning and managing clinical trials.
Full-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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A Senior Clinical Research Associate will work closely with clinical operations and the cross-functional study execution team to implement all aspects of clinical trials to support multiple clinical programs.
$158,000 a yearFull-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Expertise in statistical methods to support medical and scientific affairs including analysis using the clinical database for scientific meetings, publications, and internal decision-making (generally based on previously conducted randomized clinical trials.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead’s products.
$62.98 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Analyze data and interpret results from clinical trials to meet the project objectives; may work on exploratory analyses related to clinical pharmacokinetic/pharmacodynamic, translational biomarker, and/or manufacturing data.
$270,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This position plays a crucial part in ensuring the successful conduct of clinical trials in adherence to the protocols, company SOPs, GCP, and other relevant regulatory requirements, underscoring our steadfast commitment to industry regulations and standards.
$279,000 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Performs GLP, cGMP, QSR, GCP (Coordinate with external GCP auditors as required for compliance in clinical trials) and 21 CFR Part 11 audits/inspections. Regulated work conducted by SRI staff includes safety testing, clinical manufacturing and Phase I-IV clinical trials.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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As a member of the Clinical Trials leadership team, the Director will contribute to the strategic direction and operational excellence of the company’s clinical research initiatives supporting the Clinical Trial department mission.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Works with Study Biostatisticians and Clinical Research Scientists to assist with innovative trial design, simulation and execution, and develop adaptive trials software tools as appropriate.
Full-timeExpandApply NowActive JobUpdated 26 days ago
clinical trials jobs in Menlo Park, CA
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