Experienced Clinical Trials Feasibility Coordinator

Medpace; Cincinnati (OH); On-site; USD 60,000 - 100,000; Full time

Job summary

Join a forward-thinking organization as an Experienced Clinical Trials Feasibility Coordinator, where you will play a crucial role in the global clinical operations team. This position involves working cross-functionally with various teams, analyzing data to provide strategic insights on country selection and enrollment planning for clinical trials. If you have a clinical background and a passion for data analysis, this opportunity is perfect for you. Be part of a team that positively impacts patient lives and drives the development of effective medical therapeutics.

Benefits

Flexible work environment

Competitive PTO packages, starting at 20+ days

Competitive compensation and benefits package

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Community involvement with local nonprofit organizations

Discounts on local sports games, fitness gyms and attractions

Modern, ecofriendly campus with an on-site fitness center

Structured career paths with opportunities for professional growth

Discounted tuition for UC online programs

Qualifications

• 3-5 years of feasibility experience within a CRO.
• Ability to prioritize multiple projects within tight timelines.

Responsibilities

• Coordinate feasibility assessments and deliver high-quality data.
• Develop preliminary proposal strategy for site and country selection.
• Assist with review of work developed by junior coordinators.

Skills

Analytical thinking

Attention to detail

Communication skills

Project management

Education

Bachelor's degree in life sciences

Master's or PhD in life sciences

Job description

Experienced Clinical Trials Feasibility Coordinator

Job Locations

United States-OH-Cincinnati

Category

Feasibility & Proposals

Job Summary

We are currently seeking an Experienced 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, as well as through analyzing data from internal and public data sources , 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 and an interest in data analysis, 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;
• 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;
• As needed to support feasibility strategy, coordinate outreach to investigative sites to obtain indication and protocol specific feedback;
• Assist with review of work developed by more junior feasibility coordinators;
• Collaborate with operational team members in preparation for bid defense meetings; and
• Support departmental process improvement initiatives and general departmental administrative functions.

Qualifications

• Bachelors degree in life sciences required, Masters or PhD preferred;
• 3-5 years of feasibility experience within a CRO;
• Analytical thinker with great attention to detail;
• Ability to prioritize multiple projects and tasks within tight timelines; and
• Excellent written and verbal 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 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.

Cincinnati Perks

• Cincinnati Campus Overview
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with local nonprofit organizations
• Discounts on local sports games, fitness gyms and attractions
• Modern, ecofriendly campus with an on-site fitness center
• Structured career paths with opportunities for professional growth
• Discounted tuition for UC online programs

Awards

• Named a Top Workplace in 2024 by The Cincinnati Enquirer

• 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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