Welcome page Returning Candidate? Log back in! Feasibility Coordinator Job Locations Germany-Munich Category Feasibility & Proposals 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 new graduates.

Responsibilities Coordinate feasibility assessments and deliver high quality, accurate feasibility data to internal and external teamsDevelop preliminary proposal strategy for site and country selectionPerform outreach to investigative sites to obtain indication and protocol specific feedbackPresent feasibility results to members of the proposal team to assure correct assumptions were applied and strategy is in line with our therapeutic and operational experienceCreate study-specific feasibility questionnaires, cover letters, and other feasibility-related documentsAssist project teams with preparation for bid defense meetings; andSupport departmental process improvement initiatives and general departmental administrative functions Qualifications Bachelors degree in life sciences required, Masters or PhD preferredAnalytical thinker with great attention to detailAbility to prioritize multiple projects and tasks within tight timelinesExcellent written and verbal communication skillsFluency in English languageSome clinical research experience is beneficial; andWorking 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). 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 packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-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 2024Continually 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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