Responsibilities:
- Conduct qualification, initiation, monitoring, and closeout visits for research sites
- Communicate with medical site staff and ensure investigator compliance
- Verify investigator qualifications, training, and resources
- Review medical records and research source documentation
- Verify subject eligibility and accurate data reporting
- Assess patient recruitment and retention success and offer improvement suggestions
- Complete monitoring reports and follow-up letters
Qualifications:
- Bachelor’s degree in a health or life science related field preferred
- Clinical Research Coordinator experience is advantageous
- Willingness to travel approximately 60-80% nationally
- Familiarity with Microsoft Office
- Strong communication and presentation skills
Why Medpace: Medpace is a full-service clinical contract research organization dedicated to accelerating the global development of safe and effective medical therapeutics. Joining Medpace means being part of a team committed to supporting groundbreaking drug and device development while enjoying competitive compensation, benefits, and internal growth opportunities.
What to Expect Next: Interested candidates are encouraged to apply online. Qualified applicants will be contacted for an interview. Medpace is an Equal Opportunity/Affirmative Action Employer.
WARNING: Beware of phishing scams. Medpace employees will never ask for payment as part of the application process.