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Feasibility Coordinator

Medpace

Greater London

On-site

GBP 30,000 - 50,000

Full time

30+ days ago

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Job summary

Join a forward-thinking clinical research organization as a Feasibility Coordinator, where you will play a key role in global clinical trials. This entry-level position offers a unique opportunity to work cross-functionally with clinical operations, medical, and regulatory teams. You will be responsible for conducting feasibility assessments, developing proposal strategies, and ensuring high-quality data delivery. With a supportive environment and structured career paths, this role is ideal for individuals looking to transition from academia into the industry. Be part of a mission-driven team that positively impacts patient lives through innovative research.

Benefits

Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths
Company-sponsored employee appreciation events
Employee health and wellness initiatives

Qualifications

  • Bachelor's degree in life sciences required; Master's or PhD preferred.
  • Strong analytical and communication skills are essential.

Responsibilities

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

Skills

Analytical thinking
Attention to detail
Communication skills
Project management
Clinical research knowledge

Education

Bachelor's degree in life sciences
Master's or PhD in life sciences

Tools

Feasibility databases

Job description

Job Summary

We are currently seeking a Feasibility Coordinator, who will be a member of our global clinical operations team. By working cross-functionally with our clinical operations, medical and regulatory submissions teams, researching internal and public domain databases, as well as through obtaining direct feedback from investigative sites, this individual will provide strategic insights on country selection and enrollment planning for global clinical trials. If you are an individual with a clinical background and expertise in clinical research, please review the following career opportunity. Entry-level positions are also available for those making the transition from academia into industry.

Responsibilities
  • Coordinate feasibility assessments and deliver high quality, accurate feasibility data to internal and external teams;
  • Develop preliminary proposal strategy for site and country selection;
  • Perform outreach to investigative sites to obtain indication and protocol specific feedback;
  • Present feasibility results to members of the proposal team to assure correct assumptions were applied and strategy is in line with our therapeutic and operational experience;
  • Create study-specific feasibility questionnaires, cover letters, and other feasibility-related documents;
  • Assist project teams with preparation for bid defense meetings;
  • Support departmental process improvement initiatives and general departmental administrative functions.
Qualifications
  • Bachelor's degree in life sciences required, Master's or PhD preferred;
  • Analytical thinker with great attention to detail;
  • Ability to prioritize multiple projects and tasks within tight timelines;
  • Excellent written and verbal communication skills;
  • Fluency in English language;
  • Some clinical research experience is beneficial;
  • Working knowledge of feasibility processes and databases is highly desirable.
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 5,000 people across 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.

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