Meeveem
HomeHow Meev worksJobsCompanies
Career Hub
NHS Pay CalculatorIndustry InsightsCareer GuidesRoles Library
For employersSign inFind my fit
HomeHow Meev worksJobsCompanies
Career HubNHS Pay CalculatorIndustry InsightsCareer GuidesRoles Library
For employersSign inFind my fit
Meeveem
Your career coach,
built for health professionals.

For candidates

How Meev worksNHS Pay CalculatorAll JobsCareer HubContactSign In

Popular searches

Radiographer jobsRegulatory affairs jobsMedical writer jobsNursing jobs in LondonClinical research jobsPharmacovigilance jobs

For employers

How Meeveem works for employersBook a demo
© 2026 Meeveem Ltd · Registered in England & Wales
TermsPrivacyCookies
Medpace logo

Medpace

Feasibility Coordinator

Feasibility Coordinator

LondonOn-Site
Permanent

Feasibility Coordinator

Medpace

Full-Time
Sign up to unlock the estimation.Sign up to unlock the estimation~£28,000 - £38,000per annum· Meev estimate

Posted 4 days ago

Description

Feasibility Coordinator
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 enrolment 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.

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
  • Assist project teams with preparation for bid defense meetings; and
  • Support departmental process improvement initiatives and general departmental administrative functions

Qualifications
  • PhD in life-sciences or 2 years experience in CRO (Clinical Trials) 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; and
  • Working knowledge of feasibility processes and databases is highly desirable

We ask that you please submit your CV in English

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 mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
Competitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-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.
Medpace cover
Medpace logo

Medpace

Global clinical research careers connecting UK health expertise with trials that matter

LondonContract Research1000+
Medpace logo

Medpace

Contract Research

Use your UK clinical registration to shape research that reaches patients worldwide. Medpace offers London roles where nursing and other regulated expertise strengthen trial design, safety and delivery.

Click to learn more
Medpace logo

Medpace

Contract Research

Use your UK clinical registration to shape research that reaches patients worldwide. Medpace offers London roles where nursing and other regulated expertise strengthen trial design, safety and delivery.

Similar jobs

  • Clinical Trial Site Relationship Coordinator (German Speaking)MedpaceLondon, On-Site
  • Clinical Trial Site Relationship Coordinator (Finnish Speaking)MedpaceLondon, On-Site
  • Clinical Trial Site Relationship Coordinator (Polish Speaking)MedpaceLondon, On-Site
  • Clinical Trial Site Relationship Coordinator (Hungarian Speaking)MedpaceLondon, Hybrid