Clinical Study Manager

Bernards, New Jersey US Global Channel Management, Inc.

Company Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best “talent “ for the job.


Clinical Study Manager needs 5 years relevant experience is required with a BSc, 3 years with a MS/MPH, or 2 years with PharmD/PhD/MD

Clinical Study Manager requires:

  • Phase II/III Oncology trial experience strongly preferred
  • Global trial experience strongly preferred
  • Experience working in both sponsor and CRO organizations strongly preferred
  • Candidates with a nursing diploma/assoc degree with substantial experience may be considered for this position.
  • clinical
    or basic research in a Pharmaceutical company, a Medical
    device/Diagnostic company, Academic Research Organization (ARO) or
    Contract Research Organization (CRO). CRA experience is preferred. Time
    spent directly in a medical environment (e.g. as a Study Site
    Coordinator) is also considered relevant.

Clinical Study Manager duties are:

  • Develop
    project cross-functional, integrated study plan to study start up
    (in-house) and validate and manage to the overall study implementation
    plan provided by the CRO. Participate in site selection and site
    qualification with (study team and CRO).
  • Contribute to
    operational delivery aspects of the protocol and lead document review
    & coordination for the protocol and amendments.
  • Additional medical writing tasks may involve ICF, CRF guidelines, IB and safety communications, DSUR, IND.

Additional Information


6 months