Research Coordinator Phlebotomist

6 days ago


Ottawa, Ontario, Canada Clinical Research of Ontario Full time
Clinical Study Coordinator Job Description

The Clinical Study Coordinator is responsible for coordinating and executing clinical research studies while ensuring the safety and well-being of study participants.

  • Participant Care and Support:
    • Perform clinical assessments and monitor the health of participants throughout the study.
    • Administer investigational products according to study protocols.
    • Collect and process biological specimens for analysis.
    • Monitor participants for adverse events and report findings.
  • Participant Recruitment and Engagement:
    • Screen and recruit participants based on study inclusion/exclusion criteria.
    • Obtain and document informed consent.
    • Provide education and ongoing support to participants.
  • Study Coordination:
    • Collaborate with investigators and sponsors to implement study protocols.
    • Schedule and coordinate participant visits and procedures.
    • Ensure proper storage and handling of investigational products.
  • Data Collection and Documentation:
    • Accurately document participant data in case report forms or electronic data capture systems.
    • Maintain detailed records of all study activities.
  • Compliance and Quality Assurance:
    • Ensure adherence to Good Clinical Practice and regulatory guidelines.
    • Report adverse events and protocol deviations promptly.
  • Qualifications:
    • Bachelor's degree in a Science related field.
    • Previous experience as a Clinical Research Coordinator is required.
    • Familiarity with GCP, FDA, ICH, and other clinical research regulations.


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