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Position Overview: As a Principal Statistical Programmer with a specialized focus on PK/PD, you will play a pivotal role in the design, execution, and analysis of clinical trials to support the development of our promising drug candidates.
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LCI has developed a strong clinical trials infrastructure across all its sites, enabling oncologists in urban and rural settings to accrue to cancer trials. The Levine Cancer Institute clinical trials office has a robust team devoted to Non-treatment Interventional and Retrospective Research providing similar research and statistical support.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Minimum of 5years of experience in developing software for clinical trials using the SAS system. Develop software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies.
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The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every, single interaction.
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As part of the Atrium Health Cancer Enterprise that sees over 20,000 new cancer cases per year the ideal candidate will develop collaborative relationships with the Levine Cancer Institute in Charlotte, North Carolina that will help to optimize care and to provide clinical trials for patients in Macon, GA.
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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 Investigator for our site in Charlotte, NC. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes.
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The Clinical Research Coordinator (CRC) is central to conducting and managing clinical trials, tasked with obtaining informed consent, executing study protocols, handling human specimens, and ensuring meticulous documentation and communication.
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Assists with clinical, regulatory, business, and other documentation associated with oncology research projects/clinical trials within department. Coordinates clinical, regulatory, business, and other research- related activities and documentation for clinical trials conducted, follows industry standards and applicable regulations including FDA/OHRP guidance, GCP and ICH.
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Description & SummaryA career in Digital Business Architecture will provide you with the opportunity in structuring the enterprise in terms of its governance structure, business processes, and business information.
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Participation in clinical trials can be a very rewarding experience. Participation in clinical trials can be a very rewarding experience. Not only do you get free access to cutting-edge medical treatment, but you are also contributing to science all whilst getting paid.
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The Clinical Research Associate (CRA) / Clinical Trial Liaison plays a crucial role in the preparation, execution, and oversight of clinical trials. The CRA will ensure that trials adhere to Good Clinical Practices (GCP) and client-specific procedures, while implementing Risk-Based Monitoring practices for Phase II – IV trials.
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The Clinical Trials Assistant (CTA II) performs clinical research development activities with senior research staff for the IDCRC and assists in development, implementation, and oversight of IDCRC multi-site clinical research studies (from protocol development through study closeout.
$65,000 a yearFull-timeExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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The Clinical Trial Navigator (CTN)II is a specialized research professional responsible for the coordination and administration of clinical trials under the direction of the Manager of Clinical Trial Operations and the Principal Investigator or designee.
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AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data.
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clinical trials jobs in Charlotte, NC
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