Contract (option to Perm) Clinical Research Associates

Category: CRA
Job #: 10785
Utilization: 50-100%
Location: West, Southwest, Midwest or Northeast US
Job Type: Contract to Perm
Therapeutics: No Specific TA Required

We have an opportunity with a great Partner to become a full-time part of their team. They have an immediate need for CRAs in the West, Southwest, Midwest or Northeast US with a Bachelor's Degree and at least 50% utilization. This is a contract position with the option of converting to Perm (100% utilization) within 6-12 months based on performance. This is a great way to diversify your therapeutic experience.

Job Responsibilities:
  • Act as the "Site Manager" ensuring relationship with site(s) are positive, issues are resolved quickly, and communications are strong across all verticals.
  • Assist with the development of study manuals, CRFs, monitoring standards, site study tools and other study materials as required.
  • Develop and implement site recruitment, selection and initiation plan.
  • Manage and drive patient recruitment and enrollment tracking.
  • 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:
  • Must have a minimum 3 years' recent experience as a fully dedicated Regional, Home-Based, Field Monitor for a CRO or Pharma
  • Must be located in the West, Southwest, Midwest or Northeast US and flexible on nationwide travel
  • 50% Utilization required now (100% within 6-12 months)
  • A Bachelor’s degree or experience as a nurse (or similar medical background) is required
  • Diverse therapeutic experience is a plus

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