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Clinical Research Coordinator

Job in Kimberley, Cranbrook / EK, BC, Canada
Listing for: Placements24
Full Time position
Listed on 2026-10-15
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60000 - 90000 CAD Yearly CAD 60000.00 90000.00 YEAR
Job Description & How to Apply Below
Location: Kimberley

About the Role

Our client is seeking a dedicated and organized Clinical Research Coordinator to join their team in Kimberley . This hybrid role plays a vital part in the successful execution of clinical trials, ensuring compliance with protocols and regulatory standards. You will be responsible for managing patient recruitment, data collection, and participant follow-up, working closely with investigators, study sponsors, and regulatory bodies.

This position requires strong organizational skills, attention to detail, and a commitment to advancing medical research through ethical and efficient trial management.

Key Responsibilities
  • Recruit, screen, and enroll eligible participants for clinical trials according to protocol requirements.
  • Collect, manage, and maintain accurate and complete study data, ensuring data integrity and confidentiality.
  • Schedule and coordinate study visits, including assessments, procedures, and sample collection.
  • Educate participants about study procedures, risks, and benefits, ensuring informed consent is obtained and maintained.
  • Monitor participants for adverse events and report them promptly according to regulatory guidelines.
  • Liaise with investigators, study sponsors, regulatory agencies, and other stakeholders to ensure smooth trial operations.
Requirements
  • Bachelor's degree in a life science, nursing, or related field;
    Master's degree preferred.
  • Minimum of 3 years of experience as a Clinical Research Coordinator or similar role.
  • Thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., FDA, ICH).
  • Experience with electronic data capture (EDC) systems and clinical trial management software.
  • Excellent organizational, communication, and interpersonal skills.
  • Ability to manage multiple priorities and work effectively in a hybrid setting.
Benefits
  • Competitive salary and potential for annual bonuses.
  • Comprehensive health, dental, and vision insurance coverage.
  • Retirement plan options.
  • Generous paid time off and holidays.
  • Opportunity to contribute to life‑saving medical advancements.
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