Clinical Research Associate definition

Clinical Research Associate or "CRA" means the person assigned by POI to monitor one or more Study sites.
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Clinical Research Associate or "CRA" means the person assigned by POI to monitor one or more Study Sites.
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Clinical Research Associate or "CRA" means the person assigned by ALLPHASE to monitor one or more Study Sites.
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Examples of Clinical Research Associate in a sentence

  • Completion of the Clinical Trial is defined as the date on which the closeout visit occurs between the Consultant and the Company’s Clinical Research Associate (or the Company’s Study Monitor) after the final patient enrolled in the study completes their last clinical visit.

  • All used vials will be retained in the institution's pharmacy until the Clinical Research Associate performs a complete drug accountability audit.

  • Clinical Research Associate travel time will be invoiced at an hourly rate of $150.

  • Zkoušející: Monitor: The representative (i.e., Clinical Research Associate or Clinical Monitor) employed by Sponsor, WCT or other agency appointed by WCT who is responsible for assisting Investigator with the initiation of the Study at the Centre and for monitoring the progress and performance of the Study by Investigator thereafter Monitor: Zástupce (tj.

  • Project Coordinator II, Sr. Technical Editor $95.00 Clinical Data Coordinator, Clinical Research Associate 11.

  • Clinical Research Organisation (Optional Clause) Whereas to conduct the Trial, the Sponsor has contracted the services of _____, a Contract Research Organisation with registered address in _____ and Tax ID No. _____, (hereinafter the "CRO"), to perform the following functions: _____ _____ _____ Clinical Research Associate The Sponsor has designated Mr/Ms _____ as the Clinical Research Associate (hereinafter, the "CRA") with ID No. _____.

  • Investigator XXX Zkoušející lékař XXX Monitor The representative (i.e., Clinical Research Associate or Clinical Monitor) employed by Sponsor, WORLDWIDE or other agency appointed by WORLDWIDE who is responsible for assisting Investigator with the initiation of the Study at the Centre and for monitoring the progress and performance of the Study by Investigator thereafter.

  • CEO $[***] EVP, Commercial $[***] VP, Scientific Affairs $[***] Manager, Clinical Affairs $[***] Clinical Trials Manager $[***] Clinical Research Associate $[***] Data Administrator $[***] Office Manager $[***] Consultants [***] Note: Rates may be adjusted periodically to reflect increases in compensation and/or benefit costs.

  • EXAMPLE OF PERSONNEL PROFILE - CLINICAL --------------------------------------- This study will be managed by 1 Principal Clinical Research Associate, 4 Clinical Research Associates (based in the UK, Spain and Germany) and assisted by 1 Clinical Studies Assistant.

  • Podle národních etických pokynů by pouze CRA měl mít přístup k výsledkům laboratorních testů a jiným záznamům o pacientovi/subjektu hodnocení potřebným k ověření 5.4 Monitoring The Clinical Trial will be monitored by a CRO designated Clinical Research Associate (CRA).