We are working with a fast growing organization who is seeking to bring on experienced Clinical Research Associates located nationwide. The role requires limited to no travel and offers a tremendous opportunity to partner with a growing, high-quality and innovative team.
Responsibilities
- Interact with personnel from study Sponsors, investigational sites, vendors, and functional groups to enable quality and on-time execution of clinical trials.
- Identify potential sites for participation in clinical trials.
- Perform protocol/site feasibility and Pre-Study Visits to recommend qualified sites.
- Participate in Investigator Meetings, CRA and Study Coordinator training sessions, and assist sites with study-related questions as needed.
- Provide feedback to study manuals, Case Report Form completion guidelines, monitoring plans, informed consents, recruitment materials, and monitoring tools, as needed.
- Perform Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits in compliance with the approved protocol and monitoring plan.
Requirements
- Bachelor’s degree in a life science or related field of study
- Minimum of 3 – 5+ years monitoring experience
- Oncology Radiopharmaceutical experience required