Clinical Research Associate (VA)


Category: CRA
Job #: 10642
Location: Norfolk, VA
Job Type: 1099
Rate / Salary Range: Competitive Rate

One of our Sponsor partners is looking for a Contract CRA to perform monitoring tasks for 2 clinical sites. On-site visits required at the VA location, the other site is 100% remote. Some key points of this position include:

  • Strong experience required in RBM; both as a monitor or as someone who has provided feedback to an RBM monitoring plan
  • No specific therapeutic experience is required
  • Experience monitoring / working with Women’s studies / Contraceptive studies is a plus
  • Competitive Pay Rate
Job Responsibilities:
  • Provide training to sites on the study protocol, study conduct, CRF completion and data management expectations.
  • Ensure essential document collection for completeness per regulatory requirements.
  • Serve as a liaison with Investigators, Institutions and sites to provide support during the conduct of the clinical trial and serve as a resource for protocol and procedures.
  • Demonstrate knowledge of on-site monitoring to ensure compliance with GCPs, study protocols, and SOPs.
    Manage one or multiple studies.
  • Monitor product supplies/accountability including proper storage, dispensation, and disposal.
  • Manage study completion activities including CRF collection, query resolution, record archiving and site closeout activities.
  • Review in-house data and study tables.
  • Mentor, coach and provide guidance to clinical staff as appropriate.
  • Supervise and train other employees as appropriate.
Job Qualifications:
  • Minimum 3 years' experience as a fully dedicated regional, home based, field monitor for a CRO or pharma
  • Within driving distance to Norfolk, VA; overnight hotel stay OK as needed/required

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