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These activities may occur at various stages of the clinical trials, including study start-up, maintenance, close-out, and/or archival. High school diploma/GED and at least 2 years of relevant experience in clinical trials research.
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The Chair has endowment support and a generous start-up package and will have the opportunity for close collaboration with the Brian D. Jellison Cancer Institute at Sarasota Memorial Hospital as well as other oncology centers in the area.
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May collaborate with study investigators, nurses, study coordinators, and study sponsors to coordinate study start-up activities, which include collection and distribution of regulatory, budget, contract, and coverage analysis documents.
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Serve as Contributing Scientist/Principal Investigator on GLP and Non-GLP studies, and as scientific resource for junior staff, peers and Study Directors. Method development, qualification, validation and execution of study sample analysis for evaluation of toxicological and biological endpoints in support of preclinical studies as well as for clinical studies.
$90,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Function as a Clinical Data Manager (CDM) to coordinate the day-to-day support of CDM results from study start-up through to database lock to receipt of final study outputs for clinical studies outsourced to contract research organizations.
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The candidate will be accountable for clinical trial study start up, maintenance, and close out. The Protocol Project Manager (PPM) will work within a specified oncology disease program and serve as the main point of contact between the study team including faculty and clinical research coordinators (CRC), outside entities such as sponsors, and various departments within UCSF providing support.
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As lead of the Study Core Team the CS will lead via a matrix organization Epidemiology, Biostats, Clinical Operations, Medical/Scientific Affairs, Regional, Pfizer laboratory assay group, and external team members.
$145,400 - $269,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Requires basic knowledge and techniques to conduct various experiments in molecular biology and protein chemistry and the ability to adapt to new technologies related to the research projects. Experience Required: Five years of experience in scientific or experimental research work.
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Informs Investigator Initiated Study (IIS) strategy and can act as Docent for IISs. The Associate Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions (HCPs, Patients and Payers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines, and value proposition); safeguarding patient safety (risk minimization activities and safety surveillance activities.
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Represents AbbVie at external meetings including investigator meetings, scientific association meetings, etc. Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in the design of protocols preferred.
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Here, you can apply your scientific curiosity in Biology, Animal Science, Zoology, Animal Behavior, Veterinary Technology, Dairy Science, Equine Science or similar majors to pursue advances in animal welfare and research the effectiveness, safety and toxicity of drugs in early development animal research studies.
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Research Engineer serves as principal investigator for multiple research projects investigating electronic assembly processes, assembly materials, interconnect reliability or novel assembly manufacturing equipment as they relate to existing or developmental electronic packaging technologies.
$92,000 - $107,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Additionally, duties include start-up responsibilities, eIRB/IBC/PSR submissions and overall workflow facilitation for our study start-up team. Assists in developing website or other social media for marketing/recruiting based on assigned clinical research study.
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The Research Scientist - Clinical requires a PhD degree in Population Health Sciences, Epidemiology or other clinical arena (e.g., Nursing) and a minimum of two years related postdoctoral clinical research experience.
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The research social scientist in the Animal Human Policy Center (AHPC) plays a key role in a social science research study on the federal Animal Care (AC) program, which implements that Animal Welfare Act and the Horse Protection Act throughout the United States.
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clinical research investigator study start up jobs Company: Cedars Sinai
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