Become a key player as a Clinical Research Coordinator overseeing clinical trials and ensuring adherence to GCP regulations. This role is based in office and requires exceptional detail orientation.
In this Clinical Research Coordinator position, you will manage the complete lifecycle of clinical studies including recruitment, data collection, and compliance with regulatory guidelines. Your expertise will guarantee that research protocols are followed and that participant data remains accurate and confidential.
Key Responsibilities:
• Manage all aspects of participant coordination and consent
• Ensure compliance with Health Canada and ICH-GCP
• Collect and enter study data into EDC systems
• Maintain subject files and regulatory documentation carefully
• Monitor for adverse events and communicate effectively
Requirements:
• Bachelor’s degree in life sciences or related field
• 1-3 years of clinical research experience expected
• Phlebotomy certification is required
• Familiarity with EDC systems such as Medidata
• Strong communication and organizational capabilities
Leverage your clinical research experience to enhance study conduct and maintain the highest standards for research integrity.
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