Director, Feasibility
We are currently seeking a Director, Feasibility, who will be an integral team leader within our global Proposals and Feasibility team. If you are an individual with a strong clinical background and expertise in clinical trial management, please review the following career opportunity.
Responsibilities
- Evaluate and support new clinical trial opportunities
- Working strategically with Medpace Medical Experts, Clinical Trial Managers and our Regulatory Submissions team.
- Collaborating with Investigators and international country managers
- Analysis of multiple data sources
- Strategize the most efficient scenario to conduct various studies globally.
Qualifications
- Bachelors required, Masters/PhD preferred
- 5-7years of project management/clinical trial management/feasibility experience in clinical research, CRO experienced preferred
- Analytical thinker with great attention to detail
- Thorough knowledge of feasibility processes
- Advanced understanding of operational aspects of clinical trials
- Ability to work independently
- Outstanding leadership, and communication skills
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
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.
Responsibilities
- Evaluate and support new clinical trial opportunities
- Working strategically with Medpace Medical Experts, Clinical Trial Managers and our Regulatory Submissions team.
- Collaborating with Investigators and international country managers
- Analysis of multiple data sources
- Strategize the most efficient scenario to conduct various studies globally.
Qualifications
- Bachelors required, Masters/PhD preferred
- 5-7years of project management/clinical trial management/feasibility experience in clinical research, CRO experienced preferred
- Analytical thinker with great attention to detail
- Thorough knowledge of feasibility processes
- Advanced understanding of operational aspects of clinical trials
- Ability to work independently
- Outstanding leadership, and communication skills
