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ADDITIONAL JOB RESPONSIBILITIES:The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials and mixed methods research specific to LGBTQ+ populations.
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Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA) or equivalent certification, preferred. 5 years of relevant experience as a clinical research associate or clinical research coordinator is required.
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The ideal CRA will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
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Oversees the management of all research-relevant Institute components, including the Cancer Clinical Trials Office, Shared Resources, Disease-specific/Strategic Centers, Office of Community Engagement, Office of Diversity, Equity, and Inclusion, and education programs.
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The Clinical Research Site Director will join a global company dedicated to facilitating clinical trials and clinical research for the pharmaceutical, medical device and biotechnology industries.
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The SCI - Clinical Trials Office (SCI CTO) is an integral component of the Stanford Cancer Institute since the vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting.
$109,557 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The ideal candidate will have Senior Clinical Research Coordinator Experience and strong management skills. Ensure that all clinical trials are conducted according to GCP, FDA, and ICH guidelines, as well as sponsor and protocol requirements.
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Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts.
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Three years of experience in clinical research in a medical/behavioral setting, with knowledge about the conduct of clinical trials, research principles, and methodologies/study design.
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Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.
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As a Clinical Research Physician, you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization.
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Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
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Coordinates implements and evaluates clinical research trials, studies and projects. + Assists in writing research grants, publications in medical and nursing literature, study materials, brochures and correspondence.
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M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs.
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Most trials don't require much effort and will be located near you. Potentially get paid to access the most cutting edge medicines combating your disease. Whether you are healthy, or have a specific illness, we'll connect you with the right trial.
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clinical trials research jobs Title: research in Brookhaven, GA
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