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Global Channel Management, Inc. jobs

  1. Clinical Supplies Management Specialist

    Madison, NJ
    Clinical Supplies Management Specialist needs 6+ years of Clinical Supply / Clinical Packaging / Project Coordination experience...
  2. Clinical operations associate

    Irvine, CA
    Clinical operations associate needs B.A/B.S. with some experience in a clinical research environment Clinical operations associat...
  3. Regional Operations Manager

    Corona, CA
    Regional Operations Manager needs 5 years monitoring experience in a pharmaceutical or device company or clinical research organiz...
  4. Sr. Associate Clinical Trial Management Payrolling

    Irvine, CA
    Sr. Associate Clinical Trial Management Payrolling needs (4) years clinical research experience or related experience with a Bache...
  5. Research and Development

    Cincinnati, OH
    3 days, 8hrs/day, Tuesday-Thursday Research and Development needs 4 year Science/Technical or higher degree Research and Dev...
  6. Scientist III

    Irvine, CA
    Scientist III needs ocular therapeutics experience Scientist III requires: Masters or bachelors degree in biology or related fi...
  7. Sr. Associate Clinical Trial Management

    Irvine, CA
    Sr. Associate Clinical Trial Management needs (4) years clinical research experience or related experience with a Bachelors Degree...
  8. SR. IxRS Lifecycle Support Specialist ( remote)

    Irvine, CA
    SR. IxRS Lifecycle Support Specialist needs 5 7 years working with IxRS vendors SR. IxRS Lifecycle Support Specialist requires:...
  9. Program Manager Clinical Development

    Madison, NJ
    Program Manager Clinical Development needs 4 years of clinical/research experience in the pharmaceutical/device industry Program...
  10. Clinical systems reporting associate

    Irvine, CA
    Clinical systems reporting associate needs Basic understanding of Good Clinical Practices, ICH guidelines, PhRMA code, clinical re...
  11. Clinical Technical Writer

    Madison, NJ
    Clinical Technical Writer needs 2 years' experience in Regulatory Affairs experience Clinical Technical Writer requires: Minimu...
  12. Safety Surveillance Associate III

    South San Francisco, CA
    Safety Risk Leads (SRLs) perform proactive Safety Surveillance (SS) and Risk Management (RM) to effect product safety signal detec...
  13. Clinical Technical Writer

    Madison, NJ
    Clinical Technical Writer needs 2 years' experience in Regulatory Affairs experience Clinical Technical Writer requires: Minimu...
  14. Part time Product Researcher

    Mason, OH
    Monday- Friday-30 hours max per week Part time Product Researcher needs hair Care Products Research systems and activities experi...
  15. Clinical research specialist

    Irvine, CA
    Clinical research specialist needs 2 years experience in clinical research Clinical research specialist requires: Strong working...

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