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Global drug and device development services

Project Manager 2 - Laboratory

Project ManagementConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's degree or local equivalent in Science, Business, or a related field.
  • At least 2 years of experience working in a clinical laboratory, clinical trials, or customer management/account management role in a life science-related organization.
  • At least 2 years of project management experience in a service area serving clinical trials, such as IVRS, Clinical Supplies Packaging and Distribution, Medical Imaging, Data Management, or Electronic Data Capture.
  • Working familiarity with Word, Excel, and PowerPoint.
  • Must have the legal right to work in the country where the role is based.

Responsibilities

  • Act as the sponsor's main contact for central laboratory services, following up and responding to clinical study-specific inquiries from sponsors, physicians, clinical research associates, contract research organization representatives, and the ICON Site Services Department.
  • Review newly assigned protocols and amendments; coordinate and manage completion of the Clinical Laboratory Worksheet and communicate information as required to other departments within ICON Laboratories and, where appropriate, ICON Clinical CRO.
  • Enter protocol parameter information into PACS/ICOLIMS and other systems for new or amended protocols; prepare and quality-check clinical study-specific materials.
  • Set and maintain communication guidelines throughout each study by creating and updating the study-specific Communication and Escalation Plan; ensure adherence to the protocol-specific monitoring plan; maintain clinical study-specific files and ensure documents are properly maintained and archived at study closure.
  • Provide sponsors with study management reports and support with the ICOLabs system; inform the team leader about study progress.
  • Proactively monitor the study budget.
  • Set timelines for and monitor the progress of shipment requests for storage samples, and verify data.
  • Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meetings, Bid Defenses, or Initiations.
  • Develop new tools and train new employees.
  • Perform additional relevant responsibilities as requested by management.

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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