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Reporting to the Clinical Research Manager of Blood & Marrow Transplantation and Cell Therapy (BMT-CT), the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to to manage data, enroll and follow patients on trial, and assist with regulatory and financial requirements of the trials.
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Reporting to Clinical Research Manager for Radiation Oncology, the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to manage data, enroll and follow patients on trial and assist with regulatory and financial requirements of the trials.
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With its foundations in engineering disciplines, the company's platforms vertically integrate proprietary hardware, software, bioinformatics, chemistries, and molecular biology to advance basic research, target validation, and clinical trials.
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For more information, please visit our website at Clinical Research AssociateA 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 yearExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The Pediatric Oncology Research Nurse (R-RN2) will be under the direction of the Associate Director of Pediatric Oncology Clinical Research, applying medical knowledge and experience to oversee and direct clinical course of research participants in clinical trials.
$154,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month 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.
$309,703Full-timeExpandUpdated 18 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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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.
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Working knowledge of clinical research, Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials. Partner with other clinical research colleagues to meet business needs in the field including site re-training, data collection for timely database locks and resolution of critical issues.
$105,000 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Weve developed a proprietary AI-guided antibody discovery platform as a solid foundation for innovative biologics with diverse formats (e.g. mAb, bispecific antibody and fusion proteins), and other diverse modalities such as ADC, mRNA, and CART. Well-funded and supported by our unique research, development, and clinical validation ecosystem under our corporate umbrella, the team encompasses industry veterans with proven track records of bringing novel biologics to global clinical trials.
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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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Location: Redwood City, CA or HybridPrimary Responsibilities• Working cross-functionally with R&D, Medical Affairs, Customer Success, Laboratory Operations, Clinical Operations, Engineering, Marketing, and Business Development teams to collect requirements and create/maintain a product roadmap that addresses clear business goals.
Full-timeExpandUpdated 18 days ago - UpvoteDownvoteShare Job
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Significant experience participating in cross-functional projects and teams with responsibilities related to clinical trials, pharmacovigilance or other drug development activities. Thorough knowledge of standards, systems, policies and procedures that enable QMS operations and compliance within the biopharma industry, including Good Laboratory Practices (GLP), Good Clinical Practices (GCP), Good Clinical Laboratory Practices (GCLP), Good Pharmacovigilance (GVP) and Electronic Systems Compliance (ESC.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Interactswith HCPs as a scientific resource to support activities aligned with the Medical Plan including advisory boards, speaker development and clinical trials. Collaborate with medical affairs and clinical organization to support patient enrollment in our companys sponsored clinical trials with site recommendations.
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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
clinical trials jobs in Palo Alto, CA
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