Clinical Research Associate (FL)

Category: CRA
Job #: 10636
Location: Florida
Job Type: 1099
Rate / Salary Range: Competitive Rate

One of our Sponsor Partners is looking for a long term relationship with a Contract CRA to work on a Phase III Oncology Hematology Study in Florida.  Must be able to start immediately and have at least 50% utilization available.

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.
  • Oversee management of patient recruitment and enrollment tracking.
  • Provide training to sites on the study protocol, study conduct, CRF completion and data management expectations.
  • Complete site qualification, site initiation, interim/routine monitoring and closeout visits.
  • Ensure essential document collection for completeness per regulatory requirements.
  • Demonstrate knowledge of on-site monitoring to ensure compliance with GCPs, study protocols, and SOPs. Manage one or multiple studies.
  • Monitor product supplies/accountability.
  • 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; this experience should be recent (i.e. - no longer than 2 years ago).
  • Experience working within Oncology studies required with experience in Oncology Hematology being a plus
  • Willing to travel as required.
  • Proficient with EDC

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