Medpace is seeking interns to support the Regulatory Submissions team within the Site Activation and Maintenance (SAM) Department to maintain start-up timelines, review and collect regulatory documents, and proactively identify solutions to regulatory issues.
Requirements
- Knowledge of Microsoft Office
Responsibilities
- Provide support to the study start-up team through completion of compliance tasks
- Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF)
Other
- High School Diploma, pursuing Bachelors degree in business or life science preferred
- Excellent organizational and prioritization skills
- Availability to work a minimum of 20 hours per week in our Cincinnati, OH office. Full-time preferred.
- Travel: None
- Flexible work environment
