Senior Clinical Research Associate
Company: MEP Health
- Location: Overland Park, United States
- Seniority: Senior
- Employment type: Full-time
- Posted: Today
- Offer language: English
Job description
Clinical Trial Monitor (Phase I, Healthy Volunteers)
Conduct independent monitoring for Phase I clinical trials across local research facilities and external investigator sites.
Key Responsibilities
- Perform monitoring visits and oversee on-site trial activities.
- Review and verify trial data, regulatory documents, and other study documentation.
- Assess protocol compliance and ensure adherence to study requirements.
- Identify discrepancies, document findings, and prepare monitoring reports.
- Coordinate with site personnel and internal clinical operations teams to resolve issues and support quality.
Qualifications & Skills
- Experience monitoring clinical trials and evaluating source data/documentation.
- Strong understanding of clinical protocol requirements and regulatory expectations.
- Excellent attention to detail, documentation skills, and analytical ability.
- Effective communication and collaboration with cross-functional stakeholders.
- Ability to work independently and maintain high quality and compliance standards.
