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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