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Familiarity with data management and visualization tools and collaborating with computational biology to analyze complex data sets emerging from clinical trials. Knowledge of clinical trial methodology, regulatory requirements governing clinical trials, companion diagnostics/in vitro diagnostics, protocol design, and/or experience in development strategy preferred.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Work closely with GxP Quality Assurance and functional areas responsible for the conduct of clinical research (e.g., Clinical Operations, Clinical Development, Biostatistics and Data Management, Pharmacovigilance, etc.
$230,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Working to ensure all 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 Client’s products.
ExpandApply NowActive JobUpdated 10 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.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Clinical Operations plays a key role in ensuring all Client 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.
$64 an hourExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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By unlocking the information present in microbial cell-free DNA, we're helping doctors quickly solve their most challenging cases, providing industry partners with access to the microbial landscape to accelerate biomarker discovery and clinical trials, discover novel microbes, to ultimately reduce patient suffering worldwide.
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As such, you will provide scientific input into design & implementation of clinical trials, their delivery, clinical data review and data cleaning, interpretation of results, reporting successfully on time, and activities required for worldwide registration of the product ( clinical input to NDA/BLA.
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Comprehensive knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials. experience with EDC and IXRS set up and development and/or review of clinical data management conduct (e.g. eCRFs, CRF guidelines.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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You will act as a liaison between cross-functional groups to effectively execute clinical trials. Our client has a strong pipeline that has recently started to gain attention due to promising clinical data.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Job Description POSITION OVERVIEW:Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas. Responsible for Clinical Operations activities conducted by the affiliate that are required by local regulations and/or usual practice to support clinical trials.
$185,350ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Proven experience in data management within clinical trials or a related field. Our client is seeking an experienced Clinical Data Manager to ensure the integrity and accuracy of data collected through Case Report Forms (CRFs) and other tools.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Collaborate with Clinical Development (including PV/Safety), Regulatory Affairs, and Development Operations (including Clinical Operations, Data Management, and Biostatistics), CROs and clinical sites to support overall GCP compliance and inspection readiness.
$230,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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They will work with a multidisciplinary team that includes data scientists, molecular biologists, clinical laboratory scientists, and physicians to support key company objectives that include automation and process optimization of the UroAmp assay pipeline, expansion of UroAmp-supported drug trials, and development of novel NGS assays and applications.
$160,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all CDS activities including selection and application of data acquisition standards, Data Management Plan, selection of quality risk indicators, third party study data due diligence.
$155,900 a yearFull-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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G., patient enrollment, site selection, and data collection) with other BeiGene functions (primarily those represented on CST) to support clinical trials delivery within the drug development process.
Full-timeExpandApply NowActive JobUpdated 9 days ago
clinical trials data jobs in San Mateo, CA
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