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The person will support Infectious Disease Physician Investigators in clinical research ranging from observational trials to investigational drug/product trials, including investigator-initiated, government funded, and industry-sponsored trials.
$42,953 - $77,315 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Interface with UVA investigators, the Clinical Trials Office, contracting, IRB etc. Responsibilities for the Director will include support for the UVA/Riverside Clinical Trials Alliance and all its activities and support for program building for the Riverside Clinical Trial Service Line and Clinical Trials Office.
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As a part of Clinical Trials Scientific Affairs, the Principal Scientist will support testing, method development and validation. Collaborate with Research & Development, Scientific Affairs, and Laboratory staff in any way applicable to support Clinical Trials.
$115,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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Project management skills to oversee the administrative operations of the clinical trials program; knowledge of strategies for recruiting human subjects. It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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Assist with Otsuka's clinical trials program, including registrational, post-marketing and Investigator-Sponsored Trials (ISTs), health economic outcomes research, other specific medical collaborations; provide clinical expertise and feedback regarding operational management of clinical trials to ensure optimal site selection and performance.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Thermo Fisher Scientific values the health and wellbeing of our employees.
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The Associate will be a member of the Biorepository and Biomarker Core and be involved in clinical trials, translational research, and basic science research. · Clinical data extraction for biomedical research and clinical trials.
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A Clinical Research Coordinator I is asked to perform an increasing complexity of tasks to facilitate clinical trials at Virginia Mason, working with a variety of sponsors ranging from large pharma and biotech sponsors to small non-profit grant awards.
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Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) is preferred. Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification, along with a minimum of two years additional professional experience, will be considered in place of degree.
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This role plays a pivotal role in coordinating and overseeing clinical operations of all assigned Clinical Research Nurse and Clinical Trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research studies.
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This role will be within the ophthalmology program and will be responsible for management of the day-to-day operations of one or more phase 1-3 clinical trials including trial start up, conduct and close out activities.
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Act as a clinical research pharmacist consultant by collaborating with domestic and international clinical research networks to develop and implement clinical trials, direct start-up activities, coordinate clinical site preparation/renovation, assess factors that may significantly affect a site’s clinical research and pharmacy capacity/operations, and devise solutions and/or approaches to mitigate potential issues.
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Job DescriptionJob SummaryWalgreens RWE Real World Evidence Clinical Trials is seeking an Account Director, RWE Clinical Trials with proven business development, client management, and stakeholder management skills to drive the success of the Walgreens RWE Clinicals Trials business segment.
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With 15+ years of experience in this space, our teams have supported 1000s of clinical trials, 100s of EDC builds for a multitude of Sponsors/CROs. With a long-standing alliance with Medidata (now Dassault Systems), the leading EDC platform solution provider, we have been successfully implementing Medidata’s best-of-the-breed products to help execute very complex mega-trials for our premium customers.
ExpandApply NowActive JobUpdated 7 days ago
clinical trials jobs Title: operations sr specialist
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