Feasibility Coordinator

Medpace; London; On-site; GBP 30,000 - 50,000; Full time

Job description

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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