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Medpace

Global CRO delivering full-service clinical trials

Director of Feasibility & Proposals

Proposal ManagementConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree is required; an advanced degree is preferred.
  • At least five years of project management or clinical trial management experience in clinical research is required; contract research organization experience is preferred.
  • Advanced knowledge of drug development, clinical trial management, operational procedures, and Good Clinical Practice guidelines is required.
  • The candidate must demonstrate the ability to interact effectively face-to-face with sponsors and represent the company in external settings.
  • The role requires strong leadership, writing, problem-solving, time-management, planning, organizational, written and verbal communication, and quality decision-making skills.

Responsibilities

  • Directly manage the proposal team.
  • Mentor and lead proposal writers preparing proposals, rebids, and exhibits, ensuring strategic quality control and adherence to timelines.
  • Review requests for proposals, identify capacity issues, and negotiate deadlines with Business Development Executives as needed.
  • Participate in pre-request-for-proposal client meetings.
  • Partner with Business Development, Medical, and Operations personnel to design effective proposals.
  • Contribute strategic operational content to proposals.
  • Review and revise proposal content to articulate a clear, compelling trial execution strategy.
  • Participate in client discussions and respond to requests for information after proposal delivery.
  • Lead enhancements to proposal development tools and processes.
  • Stay current on industry tactics and strategies related to proposal development.
  • Perform other projects and responsibilities as assigned.

Desired Qualifications

  • Contract research organization experience.
  • An advanced degree.

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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