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Medpace

Global CRO delivering full-service clinical trials

Feasibility Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in life sciences is required.
  • A minimum GPA of 3.5 is required.
  • Five years of feasibility experience within a contract research organization (CRO) is required.
  • Prior experience managing staff is required.
  • Ability to prioritize multiple projects and tasks within tight timelines is required.
  • Excellent written and verbal communication skills are required.

Responsibilities

  • Conduct feasibility assessments for strategic or high-priority clients in support of proposal development for new business opportunities, and provide accurate feasibility data to internal and external teams.
  • Present feasibility results to proposal-team members to ensure correct assumptions are applied and strategy aligns with therapeutic and operational experience.
  • Coordinate outreach to investigative sites as needed to obtain indication- and protocol-specific feedback in support of feasibility strategy.
  • Manage, mentor, train, and guide more junior team members, including entry-level feasibility coordinators.
  • Collaborate with project teams to support preparation of proposal documents and bid-defense meetings.
  • Suggest and support improvements to feasibility processes and templates, and implement systems to ensure timely and accurate production of feasibility data, analysis, and text.

Desired Qualifications

  • A master's degree or PhD is preferred.
  • An analytical mindset and strong attention to detail are desired.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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