Clinical Study Site Coordinator

1 week ago

Ottawa, Ontario, Canada Natural Factors Full time
Job Summary

We are seeking a highly skilled Clinical Study Site Coordinator to join our team at Natural Factors. The successful candidate will be responsible for ensuring the smooth operation of clinical studies at our site, with a focus on oncology experience.

About the Role

This is an exciting opportunity for a detail-oriented and organized individual to work in a fast-paced environment. As a Clinical Study Site Coordinator, you will be responsible for coordinating clinical trials, managing study documentation, and collaborating with internal stakeholders to ensure timely completion of projects.

Main Responsibilities
  • Study Coordination: Coordinate clinical trials from initiation to closure, ensuring compliance with regulatory requirements and company policies.
  • Documentation Management: Manage and maintain accurate and up-to-date study documentation, including case report forms, informed consent forms, and adverse event reports.
  • Collaboration and Communication: Collaborate with internal stakeholders, including investigators, monitors, and project managers, to ensure timely completion of projects and address any issues that may arise.
  • Traffic Management: Ensure that all study-related activities are conducted efficiently and effectively, minimizing delays and maximizing productivity.
Requirements

To be successful in this role, you will need:

  • A minimum of 1 year of experience in a clinical research setting, preferably in oncology.
  • Strong organizational and time management skills, with the ability to prioritize tasks and manage multiple projects simultaneously.
  • Excellent communication and interpersonal skills, with the ability to build strong relationships with internal stakeholders.
  • Proficiency in local language (English) and proficiency in French.
Estimated Salary Range

$60,000 - $80,000 per annum, depending on experience.

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