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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 24 days ago - UpvoteDownvoteShare Job
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The Sr. Manager will have the opportunity to provide category management, sourcing and contracting expertise in clinical outsourcing of global Phase 1b-Phase 3 clinical trials. MBA or JD preferred.
$70 an hourExpandApply NowActive JobUpdated 17 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. Gilead Sciences is continuing to hire for all open roles.
Full-timeExpandApply NowActive JobUpdated 19 days 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 24 days ago - UpvoteDownvoteShare Job
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Previous experience working in a matrixed environment to implement cell-based biomarker assay development and validation employing innovative approaches to support clinical trials. Formed in late 2022, with founders from Stanford University School of Medicine and Forty Seven Inc. (acquired by Gilead in 2020 for $4.9B), Inograft aims to develop life-changing therapies by applying proven stem cell therapies to areas of significant unmet medical need, including genetic disorders, autoimmune diseases, aging, and organ transplant.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 28 days 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 23 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 28 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 24 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 24 days ago - UpvoteDownvoteShare Job
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Manage and deliver technical program for the fermentation pilot plant to support field trials at customer’s sites, process scale up, new market development and production of mems. Significant travel to domestic and international locations might be required to support field trials.
$280,000 a yearFull-timeExpandApply NowActive JobUpdated 28 days 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 24 days ago - UpvoteDownvoteShare Job
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Strong knowledge of Good Clinical Practice (GCP) and US and international regulations for clinical trials. At least 1 year of Clinical Research experience in medical device clinical trials.
$145,880 a yearFull-timeExpandApply NowActive JobUpdated 5 days 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 24 days ago - UpvoteDownvoteShare Job
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You will provide programming support to statisticians in production of summary tables, data listings and graphs required for clinical trials, and CDISC datasets for regulatory submission. This position requires a comprehensive knowledge of SAS and CDISC standards, project and resource management, regulatory filing experience, and a broad understanding of the pharmaceutical drug development process.
$205,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Supports practices relating to pharmacy dispensing based on IRB approved clinical trials. Knowledge of Medical terminology and abbreviations; pharmacology and pharmacological nomenclature; medical therapeutics, pharmacokinetics, and disease states.
Part-timeExpandApply NowActive JobUpdated 4 days ago
trials job in Belmont, CA
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