FSP CRA I (Entry Level) - open for Study Coordinators, aCRA and CTAs

Monitors investigator sites with a risk-based monitoring approach, applying root cause analysis and problem-solving skills to ensure compliance. Conducts monitoring tasks according to the approved monitoring plan and maintains regular contact with investigative sites. Ensures that required essential documents are complete and in place, and provides trial status tracking and progress update reports to the team.

Bachelor's degree in a life sciences related field or a Registered Nursing certification. Minimal clinical monitoring experience in clinical trials or health sciences field with formal training in medical terminology and anatomy. Valid driver's license where applicable.