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Global drug and device development services

Clinical Trial Associate

Clinical Research OperationsPosted on Nov 9
Full-timeWarsaw, PolandNo salary listed

About the Job

Requirements

  • A bachelor's degree in a scientific or healthcare-related field is required.
  • At least one year of experience as a Clinical Trial Associate or Study Coordinator is required.
  • Knowledge of clinical trial processes, regulations, and guidelines is required.
  • The ability to work full time from the client's office in Warsaw is required.

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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