About this role
About the Role This posting represents opportunities across Medpace’s multiple functional areas. Medpace is a global organization with over 5,000 dedicated employees focused on making a difference in people’s health and lives, offering training, growth opportunities, and flexibility across roles in clinical operations, information technology, finance, labs, regulatory affairs, biometrics, commercial operations, clinical safety, business development, medical affairs, and quality assurance.
What You'll Do
- Support the clinical trial process from study start-up to closeout within Clinical Operations, collaborating cross-functionally to ensure successful study execution.
- Contribute to IT initiatives that modernize software solutions, infrastructure, and user experiences, including software development and IT operations.
- Assist Finance & Accounting activities such as analysis, reporting, budgeting, forecasting, and period closing.
- Participate in laboratory services, including routine safety testing, biomarker analysis, bioanalytical services, imaging services, and project management efforts.
- Help ensure regulatory approvals and continued compliance by interfacing with regulatory authorities and project teams.
- Assist data collection, cleaning, and analysis across Medpace sites to produce reliable results (Biometrics).
- Support business development and the bid process, and help manage contracts for clinical trials.
- Provide medical leadership and resources for planning, execution, and reporting of studies through the Medical Department.
- Support quality assurance activities to ensure safety, data integrity, and reliability of trial and lab results.
What We're Looking For
- Not specified in the posting. Roles and qualifications vary by functional area.
Nice to Have
- Not specified.
Compensation & Benefits
- Not disclosed in the posting. The page highlights opportunities for training, growth, and flexibility within a global organization.