Entry Clinical Trials Feasibility Specialist

Medpace; Cincinnati (OH); On-site; USD 42,000 - 65,000; Full time

Benefits offered by this job

Competitive pay

Health benefits

PTO

WFH after training

Job summary

Medpace, the Cincinnati-based global clinical research organization, seeks an Entry Feasibility Coordinator to join our clinical operations team. You will analyze data from internal and public sources to inform country selection and enrollment planning for global clinical trials.

You will coordinate feasibility assessments, develop site and country strategies, and present results to ensure alignment with therapeutic experience.

Qualifications

• Bachelor's degree in life sciences required; advanced degrees preferred.
• Analytical thinker with attention to detail.
• Ability to prioritize multiple projects within tight timelines.
• Excellent written and verbal communication skills.

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.
• Coordinate outreach to investigative sites to obtain indication and protocol specific feedback as needed to support feasibility strategy.
• Assist project teams with preparation for bid defense meetings.
• Support departmental process improvement initiatives and general departmental administrative functions.

Skills

Analytical thinking

Attention to detail

Communication skills

Education

Bachelor's degree in life sciences

Masters or PhD preferred

Job description

We are currently seeking an Entry 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.

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 project teams with 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;
• Analytical thinker with great attention to detail;
• Ability to prioritize multiple projects and tasks within tight timelines;
• Excellent written and verbal communication skills.

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 mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office based culture with occasional WFH that provides flexibility for eligible positions after training
• Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

• A modern corporate campus designed to support collaboration and productivity
• Multiple on-site dining options in the heart of Madison Square
• Free on-site parking
• Convenient access to on-site 24-7 fitness and wellness facilities

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.