Experienced Contract Specialist

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based and hybrid Contract Specialist to join our Clinical Operations team in Munich. This position plays a key role in the study start-up and clinical trial management processes at Medpace. The Site Contract Specialist will advance the start-up of our projects. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

• Oversees negotiations of clinical study agreements (CSA´s) on a study level and drives CSA document finalization and execution, including contractual language & terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract & budget negotiators.
• Acts as first-line subject matter expert for all such CSA elements on assigned studies for internal stakeholders. Advises stakeholders on issue resolution within the context of assigned studies.
• Plans contract execution strategy for assigned studies-including forecast of site-specific contractual execution timelines with as much accuracy as possible and coordinates with internal study team stakeholders to ensure that CTA strategy is aligned with overall study start-up plans and expectations overall.
• Works closely with internal stakeholders to prepare site contractual templates, including payment terms, in order to drive successful negotiation of contracts and budgets.
• Maintains document status reports, and updates department tools/systems and team members on a regular basis;
• Collaborates with internal legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues.
• Manages site level discussions with internal team stakeholders around fair market value of investigator budgets and payment terms within corporate and industry standards during negotiation with sites.

• Bachelor's degree; preferable in Law or Sciences.
• Relevant work experience in contract management within clinical research
• Prior contract negotiation experience preferred;
• Strong attention to detail and excellent communication skills; and
• Excellent knowledge of German and English.

Travel:None

We kindly ask to submit applications in English. We would appreciate if you could indicate the status of your work permit if needed.