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Medpace

Global CRO delivering full-service clinical trials

Medical Writer - Hematology/Oncology

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

About the Job

Requirements

  • A PhD in Life Sciences with a focus in Hematology and/or Oncology research, clinical or nonclinical.
  • Ability to synthesize complex information into a clear and concise format appropriate for the target audience.

Responsibilities

  • Write, edit, and maintain high-quality, complex clinical and regulatory documents, including clinical study reports, protocols, Investigator’s brochures, and IND and NDA modules.
  • Coordinate and conduct quality control reviews.
  • Communicate and collaborate with Sponsors and Medpace subject matter experts.
  • Manage multiple projects and tasks simultaneously while meeting deadlines.
  • Maintain an understanding of and compliance with company processes, industry guidelines, and regulations.

Desired Qualifications

  • Prior experience in the CRO, pharmaceutical, or medical writing industries is advantageous but not required.

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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