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Medpace

Global CRO delivering full-service clinical trials

Proposal Writer

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

About the Job

Requirements

  • A PhD in a life science field is required.
  • Strong initiative to learn.
  • Strong written and oral communication skills.
  • Project management skills and the ability to prioritize multiple projects and tasks.

Responsibilities

  • Lead proposal planning meetings as needed to identify issues and client requirements, recommend proposal and study strategies, encourage multidisciplinary discussion among subject-matter experts, and establish timelines and deliverables while holding internal stakeholders accountable.
  • Extract relevant content from subject-matter experts and consolidate it into a meaningful proposal narrative.
  • Include relevant data visualization materials in documents.
  • Review and analyze Request for Proposal and Request for Information documents to understand client requirements and help identify missing information.
  • Identify information to address in proposal text and collate follow-up questions when additional information is needed.
  • Draft standard documents in accordance with the agreed strategy and sponsor requirements, often within expedited timelines.
  • Contribute to assigned process-improvement initiatives and support their implementation.
  • Define action plans and timelines, and manage and determine modifications needed to ensure proposal alignment with client requirements and business strategies.
  • Perform quality control and peer review, participate in document finalization, and distribute documents to the customer and internal departments.

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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