Director, Feasibility

Medpace; City of Westminster; On-site; GBP 125,000 - 150,000; Full time

Job summary

A leading clinical research organization is seeking a Director, Feasibility, to lead within their global Proposals and Feasibility team. The role involves evaluating new clinical trial opportunities and collaborating with medical experts and managers to optimize study execution worldwide. Ideal candidates should have a strong clinical background, project management experience, and great analytical skills. The organization is recognized for its impactful work, competitive compensation, and supportive work environment.

Benefits

Flexible work environment

Competitive compensation and benefits package

Structured career paths

Qualifications

• 5-7 years of project management/clinical trial management experience in clinical research.
• Thorough knowledge of feasibility processes.
• Ability to work independently in various scenarios.

Responsibilities

• Evaluate and support new clinical trial opportunities.
• Collaborate with clinical trial managers and medical experts.
• Strategize conducting studies globally.

Skills

Project management

Clinical trial management

Analytical thinking

Leadership

Communication

Education

Bachelor's degree

Masters/PhD (preferred)

Job description

We are currently seeking a Director, Feasibility, who will be an integral team leader within our global Proposals and Feasibility team. This position will evaluate and support new clinical trial opportunities by working strategically with Medpace Medical Experts, Clinical Trial Managers and our Regulatory Submissions team. By collaborating with Investigators and international country managers, as well as analysis of multiple data sources, this individual will strategize the most efficient scenario to conduct various studies globally. If you are an individual with a strong clinical background and expertise in clinical trial management, please review the following career opportunity.

Qualifications

• Bachelor's required, Masters/PhD preferred
• 5-7 years of project management/clinical trial management/feasibility experience in clinical research; CRO experience 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 is a full‑service clinical contract research organization (CRO). We provide Phase I‑IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti‑viral and anti‑infective. Headquartered in Cincinnati, Ohio, we employ more than 4,000 people across almost 40 countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Benefits

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility