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clinical research in Phoenix

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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. Home-Based Clinical Research Associate

    Precept Life Sciences is seeking experienced Regional CRAs across the country for permanent positions with several leading CROs. On average, CRAs are assigned to an average of 12 sites across 1-3 protocols. Study and site assignment will vary depending on monitoring duration/frequency, location of sites and complexity of trial. CRAs are expected to be 80% billable, with approx. 60% travel. We are looking for CRAs that are not just field monitors, but those that manage all aspects of the site ...

  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 / ...

  4. Home-Based Clinical Research Associate

    Precept Life Sciences is seeking experienced Regional CRAs across the country for permanent positions with several leading CROs. On average, CRAs are assigned to an average of 12 sites across 1-3 protocols. Study and site assignment will vary depending on monitoring duration/frequency, location of sites and complexity of trial. CRAs are expected to be 80% billable, with approx. 60% travel. We are looking for CRAs that are not just field monitors, but those that manage all aspects of the site ...

  5. Home Based Regional CRA

    Our client is currently seeking Regional CRAs with a minimum of 2 years of Phase 1 experience for a safety study. 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/sponsor communications. Conducts monitor assessments, documents, and communicates the ...