Clinical Administrative Coordinator

1 month ago


Montreal, Quebec, Canada ICON plc Full time

Join Our Team as a Clinical Administrative Coordinator

At ICON plc, our diverse teams empower us to enhance our partnerships with clients and advance our mission to improve patient outcomes.

Core Values: Accountability & Delivery, Collaboration, Partnership, and Integrity.

We aspire to be the Clinical Research Organization that consistently delivers excellence to our clients and patients at every interaction.

In this role, you will thrive in a dynamic and supportive environment, collaborating with some of the brightest and friendliest professionals in the industry, while playing a pivotal role in shaping the future of clinical research.

Key Responsibilities:

  • Be an integral member of the study team, gaining clinical and corporate insights into the conduct of clinical trials.
  • Provide comprehensive administrative support to Project Managers and Clinical Trial Managers, focusing on global inspection readiness.
  • Engage in extensive training as this is a developmental position.
  • Assist project teams with the organization and maintenance of clinical study documentation, including preparation for audits and final reconciliation.
  • Support the processing of Data Collection Forms, ensuring proper logging, tracking, and quality control.
  • Participate in quality control audits of clinical study documentation.
  • Help project teams track trial progress by updating Clinical Trial Management systems and providing access to study/client systems.
  • Run, review, and analyze study reports for accuracy, collaborating with project teams to ensure timely updates.
  • Assist in coordinating site/study-related payments as necessary.
  • Serve as a contact for clinical sites for basic inquiries and assist in project team meetings, including preparation of meeting minutes and agendas.
  • Support the coordination of various status and tracking reports, including team member tracking and training.
  • Collaborate with internal and external colleagues to achieve project objectives and timelines.
  • Keep the Project Manager or Clinical Operations Designee informed of any issues requiring attention.

Qualifications:

A Bachelor's degree or local equivalent in life sciences or a related field is required (an associate degree in nursing is also applicable).

Our success is driven by the quality of our people. We prioritize building a culture that rewards high performance and nurtures talent. Our annual bonuses reflect the achievement of performance goals for both the organization and individual contributors.

We offer a comprehensive range of health-related benefits for employees and their families, along with competitive retirement plans and life assurance, allowing you to save and plan confidently for the future.

ICON plc is committed to equal employment opportunities for all qualified applicants, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

If you require reasonable accommodation due to a medical condition or disability during the application process or to perform essential job functions, please inform us through the appropriate channels.



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