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Medpace

Global CRO delivering full-service clinical trials

Clinical Data Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a Life Science or related field is required.
  • Strong attention to detail, communication skills, and the ability to prioritize and multitask effectively are required.
  • Experience with Excel and Word is required.

Responsibilities

  • Validate entry database designs.
  • Report project metrics and data trends.
  • Identify data conflicts and issues on projects.
  • Work with personnel from global research sites to resolve data conflicts.
  • Reconcile data from multiple sources.
  • Create and update study documentation on projects.
  • Participate as part of a team on various projects.

Desired Qualifications

  • Previous experience working with research and statistical data, ideally in a pharmaceutical or contract research organization setting.

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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