User Researcher à United States

Location: Remote - fully remote opportunity, Bethesda, MD area (candidates within a 3 hour drive or easy / short plane ride to DC and Northern, VA may also be considered). All site visits will be in Bethesda, MD location.

Start Date: 03/31/2025
End Date: 07/30/2025 (extension possible)

Assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols. Ensures coordination of interim and closeout activities associated with clinical trials to ensure timelines and metrics are met and maintained throughout the study. This is a contract traveling CRA position if necessary.

• Good knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, and company SOPs.
• Good knowledge of therapeutic area assigned; oncology.
• Preferred experience working with NCI.
• Strong knowledge of ICH/GCP Guidelines and EDC process.
• Ability to establish rapport with site personnel/colleagues.

• 5+ years in clinical monitoring, in particular oncology therapeutic experience.

Ref: #568-Clinical