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The Clinical Trials Office (CTO) at UCSD's Moores Cancer Center administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical companies, and physician investigators.
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Demonstrated experience in clinical trials research including budget negotiations and invoicing per clinical trial agreement. CANCER CENTER/Clinical Trials Office. Translational research is carried out every day in the hundreds of clinical trials of promising new therapies offered through UC San Diego Health, and in the drive of our researchers and clinician-scientists who are committed to having a significant impact on patient care.
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We specialize in executive searches at all levels inR&D, Drug Discovery, Translational Biomarkers, Precision Medicine, Immunotherapy, Companion Diagnostics, Pharmaceutical Manufacturing & Clinical Trials through to commercialization.
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Quantum Leap Healthcare Collaborative (QLHC) is seeking an exceptional Data Scientist with strong analytical and computational skills to support multiple complex clinical trials in Oncology and COVID. The Data Scientist is responsible for performing data analytical and programming activities in these trials, which may be Phase I, II and III pharmaceutical trials and medical device trials evaluating new biomarkers and/or therapeutics.
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The Department of Neurology is seeking a Statistical Programmer Analyst who will support the BIOS Clinical Trials Coordinating Center's (CTCC) Research Program and Clinical Trials Unit, which manages multi-center, 20+ million dollar federally funded clinical trials and multiple site-specific pharmaceutical sponsored trials.
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The individual will also contribute to the overall CMC strategy, planning, and execution; provide regulatory documentation for all phases of clinical trials and commercialization; and play a role in CDMO management for other CMC areas including analytical and drug product.
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Description The David Geffen School of Medicine, Department of Urology is seeking to hire a Full Time Senior Study Coordinator for pharmaceutical and industry sponsored, investigator initiated, and NIH-sponsored clinical trials.
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Oversight of the creation of a compelling scientific communications and publication plan based on the clinical trials conducted within Pfizer Oncology. Oncology medical professional with strong experience (at least 9 years if MD, ClinPharm or MD-PhD, at least 15 years if PhD or PharmD) in the pharmaceutical or biopharma industry with clinical development, and/or medical affairs experience.
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The RN Clinical Trials Coordinator Senior (RN CTC) will coordinate, manage, and assist physicians in enrolling and monitoring patients on all drug-industry sponsored and the NCI-funded clinical trials for the LSUHSC Cancer Center.
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Sanofi is seeking an accomplished analytical research and development scientist to join the Analytics grou plocated in Cambridge Crossing, MA. The Analytics group combined with Synthesis Development, Biopharmacy and Early Formulation Development constitutes the Early Development organization in the US (EDUS) which provides the CMC expertise to advance projects from late-stage research through early clinical development up to Phase 2 clinical trials.
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Serve as the SME for important toxicology/Safety topics in areas such as safety biomarker analysis, genetic, endocrine, reproductive toxicology, applications of scientific methods to delineate appropriate mode-of-actions on emerging safety issues and the assessment of human relevance of the nonclinical findings in support of the planned and ongoing clinical trials.
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Regulatory Compliance: Develop and maintain an in-depth understanding of relevant regulations, guidelines, and standards (e.g., FDA, EMA, ICH) applicable to autologous and allogeneic cell therapy clinical trials.
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Independently manage interactions with clinical monitors, data management, safety, regulatory, pharmaceutical science, QA team members etc., both internally and externally including our CRO Partners, to ensure ongoing performance alignment.
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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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Implement and develop ultra-high throughput bio-analytical platforms for various chemical, pharmaceutical, and ADME screens. Interface with clinical sample submitters and coordinate resources for their study support, where applicable.
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