Key Responsibilities:
- Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with protocols.
- Communicate with medical site staff, including coordinators and clinical research physicians.
- Verify investigator qualifications, resources, and site facilities.
- Ensure accurate data reporting through medical record and research source documentation verification.
- Oversee regulatory document review and investigational product accountability.
- Assess site patient recruitment and retention success, offering improvement suggestions.
- Complete monitoring reports and follow-up letters summarizing significant findings and recommended actions.
Qualifications:
- Bachelor’s degree in a health or life science-related field.
- Previous experience as a Clinical Research Coordinator is advantageous.
- Willingness to travel 60-80% nationally.
- Proficiency in Microsoft® Office.
- Strong communication and presentation skills.
Benefits:
- Dynamic work environment with diverse responsibilities.
- Exposure to multiple therapeutic areas.
- Opportunity for career advancement, including mentoring and management roles.
- Competitive pay with potential travel bonuses.
About Medpace:
Medpace is a leading full-service clinical contract research organization (CRO), providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
Apply now to embark on a rewarding journey that impacts healthcare on a global scale.