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Responsibilities include post award invoicing and monitoring of all industry sponsored clinical trials and some other funded clinical research if the sponsor requires an invoice for payment of CPT coded items and services.
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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.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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We are seeking a highly motivated and detail-oriented Remote Clinical Research Associate III to join our dynamic team. This role is crucial for the successful execution of clinical trials in women’s fertility, where you will be responsible for overseeing site management and monitoring activities.
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Knowledge of federal rules and regulations and sponsor requirements related to research administration of grants and contracts, specifically clinical trials, required. + Works with the SOM SRMS Training Manager to implement Standard Operating Procedures for clinical research/trials.
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Contact appropriate individuals (e.g., study site staff or study site Clinical Research Associate) regarding incomplete, inaccurate, or missing photos, acetate tracings, and other Endpoint and Specialty Services Core Lab documents as required by the project.
$115,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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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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Conducts all clinical trials (studies) according to ICH GCP, local regulations, study protocol and company processes. No previous experience in clinical research years of required, but must have general medica lpractitioner diagnosis and treatment proficiency.
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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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The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials. This position is intended to support clinical research and all clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher.
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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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DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an MD or DO for our clinical research site in Atlanta, GA to serve as a sub-investigator on clinical research trials.
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