Feasibility Coordinator

TN United Kingdom; London; On-site; GBP 30,000 - 60,000; Full time

Job summary

An established industry player is seeking a Feasibility Coordinator to enhance global clinical operations. This role involves collaboration across clinical, medical, and regulatory teams, focusing on strategic insights for country selection and enrollment in clinical trials. Ideal candidates will have a solid academic background in life sciences, strong analytical skills, and the ability to manage multiple projects efficiently. Join a forward-thinking organization that values people and purpose, and be part of a team dedicated to advancing healthcare solutions.

Benefits

Flexible Work Environment

Competitive Compensation and Benefits

Structured Career Growth

Employee Appreciation Events

Health and Wellness Initiatives

Qualifications

• Bachelor's degree in life sciences required; Master’s or PhD preferred.
• Strong analytical skills with attention to detail and communication.

Responsibilities

• Coordinate feasibility assessments and deliver accurate data.
• Develop site and country selection strategies for trials.

Skills

Analytical Skills

Communication Skills

Project Management

Attention to Detail

Education

Bachelor's Degree in Life Sciences

Master's Degree or PhD

Tools

Feasibility Databases

Job description

Social network you want to login/join with:

Feasibility Coordinator Position

We are currently seeking a Feasibility Coordinator to join our global clinical operations team. This role involves working cross-functionally with clinical operations, medical, and regulatory teams, researching databases, and obtaining feedback from investigative sites to provide strategic insights on country selection and enrollment planning for global clinical trials. Candidates with a clinical background and research expertise are encouraged to apply. Entry-level positions are also available for those transitioning from academia into industry.

Responsibilities

• Coordinate feasibility assessments and deliver high-quality, accurate data to internal and external teams;
• Develop preliminary site and country selection strategies;
• Perform outreach to investigative sites for indication and protocol-specific feedback;
• Present feasibility results to proposal team members to ensure correct assumptions and strategies;
• Create feasibility questionnaires, cover letters, and related documents;
• Assist with bid defense preparations; and
• Support process improvement initiatives and departmental administrative functions.

Qualifications

• Bachelor's degree in life sciences required; Master’s or PhD preferred;
• Strong analytical skills with attention to detail;
• Ability to prioritize multiple projects within tight timelines;
• Excellent communication skills in English;
• Some clinical research experience is beneficial;
• Knowledge of feasibility processes and databases is highly desirable.

About Medpace

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV services to biotech, pharma, and medical device industries. Headquartered in Cincinnati, Ohio, with over 5,000 employees across more than 40 countries, our mission is to accelerate the development of safe and effective therapeutics through scientific discipline and local expertise.

Why Join Medpace?

We value People, Purpose, and Passion. Our work over the past 30+ years has positively impacted countless lives. Join us to make a difference tomorrow.

Perks and Recognition

• Flexible work environment
• Competitive compensation and benefits
• Structured career growth
• Employee appreciation events
• Health and wellness initiatives

Recognized by Forbes as one of America's Most Successful Midsize Companies (2021-2024) and recipient of CRO Leadership Awards from Life Science Leader magazine.

Next Steps

A Medpace team member will review your application and contact you for next steps.

EO/AA Employer M/F/Disability/Vets