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Medpace

Global CRO delivering full-service clinical trials

Medical Writer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listedIn-person

About the Job

Requirements

  • A PhD degree in a life science is required.
  • Strong computer skills and project management skills are required.
  • A high attention to detail is required.
  • Strong written and oral communication skills are required.

Responsibilities

  • Write Investigational New Drug (IND) modules, New Drug Application (NDA) modules, and other related regulatory documents.
  • Write clinical study reports, protocols, and protocol amendments.
  • Coordinate quality control reviews of those documents and maintain audit trails of changes.
  • Interact closely with the sponsor and other Medpace subject matter experts.

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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