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The Associate Director for Translational Research will partner with the AD of Clinical Science to prioritize clinical trials and partner with the AD for Community Outreach and Engagement to ensure that translational oncology initiatives are aligned with the MCC catchment area high priority cancer.
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Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Communication, Curiosity, Data, Data Analysis, Design of Experiments (DOE), Detail-Oriented, Drug Development, Drug Discovery Process, Ethics, Gene Therapy, Group Problem Solving, Immunology, Inventory Management, Laboratory, Large Group Presentations, Leading Project Teams, Life Science, Machine Learning (Ml), Medical Research {+ 9 more.
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The Research Coordinator will assist in the conduct of Clinical Trials by ensuring protocol compliance, filing adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
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Near-term focus will be on leading the legal support for supply chain, clinical trials and regulatory issues and will evolve to also include supporting commercialization capabilities. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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The Manufacturing Technician I will be responsible for conducting cGMP manufacturing of solid oral and liquid oral pharmaceutical dosage forms for Phase I and Phase II clinical trials. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
$46,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Provide internal safety monitoring for clinical trials in collaboration with the Study Medical Director and Drug Safety team. 5+ years of experience in the design and conduct of autoimmune clinical trials.
$240,000 a yearFull-timeExpandUpdated 2 months ago - UpvoteDownvoteShare Job
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Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
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The practice is actively involved in research and currently involved in multiple clinical trials. State of the art cardiology office with top tier diagnostic equipment including nuclear, echo, and vascular accreditation.
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This position is in San Diego, CA. The USC Keck School of Medicine – Alzheimer’s Therapeutic Research Institute (ATRI) is an academic institute committed to advancing the development of new treatments for Alzheimer’s Disease (AD) through innovative clinical trials.
$94,988.05 a yearExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Facilitate education & information concerning all ongoing clinical trials as well as training & monitoring research staff assigned to these protocols. The position requires demonstrated leadership skills and vast knowledge of clinical data, data registries, & clinical research activities related to pediatric hematology and oncology.
$76.45 an hourFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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The role will provide TMF SME expertise across all therapeutic areas and research phases and will be required to work closely with R&D teams and Contract Service Providers (CSPs) as clinical trials are crafted and conducted.
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Job Title: Clinical Research AssociateJob DescriptionSeeking a proactive and diligent Clinical Research Associate (CRA) to manage all aspects of clinical trials from monitoring to close-out.
$38 - $58 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Ensure that multiple novel ideas on site engagement and optimization to improve clinical trials quality and delivery are generated and considered in alignment with broader strategic initiatives.
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Within the School of Medicine, Dermatology is a high-volume and productive administrative unit, and the staff collectively manage the pre- and post-award activities for a large and diverse portfolio of sponsoring agencies, working with federal, industry and non-profit sponsors on contracts, grants and clinical trials.
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As an extension to the Avacare study teams, this position will embed with study teams to support the identification and scheduling of eligible patients into clinical trials. + Ability to read and understand protocols and informed consents for clinical trials, and assess subject eligibility criteria.
$58,800 a yearFull-timeExpandApply NowActive JobUpdated Today
clinical trials jobs in San Diego, CA
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