Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
Office based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry renowned onboarding and training programs designed to accelerate professional development
Ongoing training and continuous learning opportunities throughout your career
An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
Competitive compensation programs that recognize and reward performance
Comprehensive health, wellness, retirement, and PTO benefits
Office based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
End-to-end management of the clinical study agreement (CSA) process for global, multi-site clinical trials
Develop the study-specific CSA strategy with the Sponsor and internal stakeholders
Develop country-specific CSA templates
Present progress to internal and external stakeholders ensuring deliverables are met within agreed upon timelines.
Bachelor’s degree in life-sciences or relevant legal or business field;
Clinical Trial experience;
CRO experience preferred;
International Contract and budget negotiation experience;
3+ years of management or oversight experience;
Ability to effectively influence others;
Exceptionally strong communication skills;
Advanced knowledge of Microsoft Word, Excel, and PowerPoint.
