Spring 2021 Intern - Clinical Trial Study Start Up
Job Summary
Our clinical operations activities are growing rapidly, and we’re currently seeking several part-time, office-based interns to support groups within our Site Activation and Maintenance department. These groups play a key role in the study start-up and clinical trial management process at Medpace. If you want an exciting position with potential to grow into a full-time role upon completion of your degree, then this is the opportunity for you!
Responsibilities
We are considering interns for the following groups:
Regulatory Submissions
- Efficiently manage and successfully execute all aspects of study start-up
- Collaborate with Institutional Review Boards (IRBs)
- Prepare regulatory documents, including Informed Consent Forms
Site Payments
- Develop, maintain, and analyze investigator grant cost estimates budgets for Phase I-IV clinical research projects from Request for Proposal (RFP) through project completion
- Coordinate the calculation of periodic payments to investigators
- Assist with monthly/quarterly IG project evaluation, including estimating, analyzing, and forecasting IG revenue/expenses by project in support of company revenue recognition
Site Contracts
- Responsible for preparing, negotiating, tracking and finalizing the Confidentiality Agreements (CDA), Clinical Trial Agreements (CTA), Budgets and Letters of Indemnification (LOI) as well as Amendments to these documents, as needed
- Manage all required contractual agreements with investigator sites
- Liaises with internal customers to review contract or budget areas that impact final execution of site contracts
Qualifications
- High School Diploma, pursuing Bachelors or Masters degree in business or life science preferred
- Excellent organizational and prioritization skills
- Knowledge of Microsoft Office
- Availability to work a minimum of 20 hours per week in our Cincinnati, OH office