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clinical research in Houston

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  1. Director of Clinical Systems and Pharmacology (Located in New Jersey)

     Fantastic opportunity in northern New Jersey for an expert Director of Clinical Systems and Pharmacology!  The individual will be based in the Department of Clinical and Exploratory Pharmacology, and will also be a member of the Interdisciplinary Program in Pharmacometrics which links pharmacometric experts across the Scientific Core Platforms.  You will also be involved with modeling activities and as appropriate serve as the project team representative. Working with internal and external ...

  2. Clinical Project Manager (Global)

    Global PM Desired Skills & Experience •          College/University degree in life sciences, RN preferred •          At least 5 years of prior industry experience •          At least 2 years of experience at a position of Clinical Project Manager •          Previous CRO experience required •          Therapeutic experience - Oncology a plus. •          Participation in at least three clinical research projects in the capacity of a Clinical Project Manager •          Proficiency in standard MS ...

  3. Home Based Regional CRA

    Our client is currently seeking contract and permanent direct-hire Regional CRAs with a minimum of 2 years of experience in Cardiovascular studies, preferably in Myocardial Infarction and/or device.   Major Roles and Responsibilities: Demonstrates management of all clinical investigative sites according to the Federal Code of Regulations, Good Clinical Practices, ICH Guidelines, local regulations, and Clinipace SOPs and/or Sponsor SOPs. Creates quality written trip reports, tracking, and site ...

  4. Senior Clinical Research Associate

    We are currently looking to hire Permanent Regional CRAs Job Description   The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, ...