Director, Feasibility

Medpace; London; On-site; GBP 80,000 - 120,000; Full time

Job summary

A leading clinical research organization is seeking a Director, Feasibility, who will assess new clinical trial opportunities. This role requires a strong clinical background and expertise in trial management, driving collaborations across teams to enhance study efficiency globally.

Benefits

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths for professional growth

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualifications

• 5-7 years of project management/clinical trial management/feasibility experience in clinical research.
• Thorough knowledge of feasibility processes.
• Advanced understanding of operational aspects of clinical trials.

Responsibilities

• Evaluate and support new clinical trial opportunities.
• Work strategically with Medical Experts and Regulatory Submissions team.
• Collaborate with Investigators and country managers.

Skills

Analytical thinker

Attention to detail

Leadership

Communication

Education

Bachelors degree

Masters/PhD preferred

Job description

Responsibilities

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

• 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). 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, employing 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.

Medpace Perks

• 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

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets

• 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

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.