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clinical research in Phoenix

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  1. Patient Recruitment Specialist

    Radiant Research, Inc. (radiantresearch.com) is comprised of 22 wholly-owned premier clinical research centers nationwide. Our clinical research centers provide a critical service to biopharmaceutical companies by recruiting study participants into clinical research, conducting the clinical research protocol and collecting the data necessary to support the safety and efficacy of the drug company's product to the FDA. Our client list includes every major pharmaceutical company and contract research ...

  2. Budgets and Contracts Account Manager

    Clinical Research Advantage, Inc. (CRA) is the largest Clinical Trial Management Network in the U.S. servicing the pharmaceutical, biotechnology, and medical device industries. CRA has completed over 1,800 clinical trials in its 20 years of existence. CRA is comprised of community-based Investigators with an experienced staff of Clinical Research Coordinators and currently operates at over 70 locations across the country.   CRA is currently seeking a full-time Budgets & Contracts Account Manager in ...

  3. $5K Sign On Bonus- CRA  Monitors Needed - Set Yourself Up for Success

    CRAs - Join Covance and receive a $5000 Sign On Bonus! Meet the CRA hiring team at the ACRP conference - email [email removed].   Set yourself up for SUCCESS with Early Clinical Development! Now is the time to join our growing business where you have supportive management and a cohesive team. At Covance, you are not just a number. We value you and your hard work...we want you to succeed.   URGENT Need for Oncology Monitors! Calling all Experienced Clinical Research Associates / CRAs / Monitors ...

  4. Senior Clinical Research Associate

    Senior Regional Clinical Research Associate Identifies potential investigators, contract research organizations and outside vendors. Collects required documentation for review by Project Manager to make a selection decision. Conducts site visits pre-study, at study initiation, at regular intervals during the study and at study closeout. Prepares a variety of reports and letters in accordance with study SOPs and industry standards. Collects, reviews and processes regulatory documents. Ensures ...