Entry Level Life Sciences Info Session - Munich - October 27th
About the role
Medpace is hosting a virtual info session for Bachelor's, Master's and PhD students in life sciences.
The session is scheduled for October 27th at 11:00 AM; a pre-screening will be conducted and selected candidates will receive a MS Teams invite to join.
Responsibilities
- The event will present example entry-level positions and discuss their responsibilities.
- Regulatory Submissions Coordinator: prepare, review and file clinical trial applications for Germany, Austria and Switzerland (DACH); communicate with research sites in DACH to collect essential documents before site enrollment; provide input on regulatory submissions documents and maintain study start-up timelines through internal and external collaboration.
- Clinical Research Associate: complete a comprehensive training program to monitor sites independently; travel to non-local, national study sites 60-80% of the time; communicate with medical staff and clinical research physicians on site.
- Clinical Trial Site Relationship Coordinator: provide ongoing site support including feasibility assessments and business opportunity discussions; act as site relations partner to build and retain assigned-site relationships; conduct regular performance reviews to ensure quality study delivery.
Requirements
- Qualification: Bachelor's, Master's or PhD in Life Sciences or related fields.
- Location requirement: willing to work office-based in Munich.
Preferred qualifications
- Preferred: interest in office-based roles with on-site mentorship and participation in onboarding and ongoing training programs.
- Preferred: interest in roles with defined career paths and clear advancement opportunities.
Skills
Collaboration and communication skills to work with physicians, scientists and cross-functional teams in an interactive environment that supports decision making and continuous learning.
Work arrangement
Office-based culture with occasional work-from-home flexibility for eligible positions after training.
Compensation
Medpace offers competitive compensation programs that recognize and reward performance.
Benefits
- Benefits highlighted include comprehensive health, wellness, retirement and PTO benefits, company-sponsored social events, and structured onboarding plus ongoing training.
- Please note: benefits may vary by country.
Company context
Medpace is a full-service clinical CRO providing phase I–IV clinical development services to biotechnology, pharmaceutical and medical device industries; the company employs more than 6,500 people across 40+ countries and leverages in-country regulatory and therapeutic expertise across major therapeutic areas.
Joining Medpace offers exposure to cross-functional collaboration and work focused on bringing therapies to market while supporting scientific excellence and patient outcomes.
Additional employer context: the source lists Purpose-Driven Work, a Collaborative Culture, accessible leadership, Continuous Growth & Development, and other employee benefits.
Relevant source disclaimer
A Medpace team member will review applications and contact candidates whose profiles match current needs; only selected applicants will be contacted.