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Medpace

Global CRO delivering full-service clinical trials

Director of Proposals

Proposal ManagementConfirmed live in the last 24 hours
Full-timeLondon, UKNo salary listed

About the Job

Requirements

  • A bachelor's degree is required; an advanced degree is preferred.
  • At least 5 years of project management or clinical trial management experience in clinical research is required; CRO experience is preferred.
  • Advanced knowledge of drug development, clinical trial management, operational procedures, and Good Clinical Practice guidelines is required.
  • The candidate must effectively interact face-to-face with sponsors and represent the company in external settings.
  • Strong leadership, writing, and problem-solving skills are required.
  • Superior time management, planning, organizational, written and verbal communication, and quality decision-making skills are required.

Responsibilities

  • Directly manage the proposal team.
  • Mentor and lead Proposal Writers in preparing strategic proposals, rebids, and exhibits, with rigorous 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 Operational personnel to design effective proposals.
  • Contribute strategic operational content to proposals.
  • Review and revise proposal content to ensure a clear, compelling strategy for executing the trial is articulated.
  • Participate in client discussions and respond to requests for information following proposal delivery.
  • Lead enhancement of proposal development tools and processes.
  • Stay abreast of industry tactics and strategies regarding proposal development.
  • Undertake other projects and responsibilities as assigned.

Desired Qualifications

  • CRO 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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