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Global drug and device development services

Global Clinical Trial Associate

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeWarsaw, Poland

About the Job

Requirements

  • A bachelor's degree in a scientific or healthcare-related field is required.
  • At least 1 year of experience as a Study Coordinator or Clinical Trial Associate is required.
  • Knowledge of clinical trial processes, regulations, and guidelines is required.
  • Fluent English is required.
  • The employee must have the legal right to work in the country where the role is based.

Responsibilities

  • Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
  • Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
  • Support the preparation of study-related materials, such as informed consent forms and case report forms.
  • Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
  • Contribute to the tracking and reporting of clinical trial metrics and milestones.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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