Global Clinical Trials Feasibility Coordinator

Medpace

Cincinnati (OH)

On-site

USD 42,000 - 65,000

Full time

13 days ago
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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

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.

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