Director - Study Start-Up Project Management
Medpace, Inc.•Cincinnati, OH
•Onsite
About The Position
We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the Clinical Operations leadership team and requires a strong understanding of how study start-up and regulatory submissions are integrated with other clinical operations functions throughout Medpace. Study Start-Up/Regulatory Submissions experience within a CRO is required.
Requirements
- Bachelor’s degree in Life Sciences or related field
- 8+ years as a study start-up senior leader within a CRO
- Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills
- Strong customer focus with ability to manage challenging priorities and remain flexible and adaptive in stressful situations
- Excellent written and oral communication
- Experience managing and developing a team
Nice To Haves
- Advanced degree is preferred
Responsibilities
- Contribute directly to the growth and strategic development of a large, global Study Start-Up team
- Develop and identify continuous improvement opportunities of internal processes
- Oversee Study Start-Up/Regulatory Submissions activities and timelines to ensure they are in accordance with Medpace standard operating procedures and study protocols
- Provide input on new business development opportunities
- Develop and maintain relationships with clients
Benefits
- Competitive bonus program
- Sign-on/relocation bonus
- Equity awards
- Comprehensive health, wellness, retirement, and PTO benefits
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What This Job Offers
Job Type
Full-time
Career Level
Director
