Support clinical research initiatives as a Clinical Research Unit Coordinator. This role focuses on project management, clinical data oversight, and ensuring adherence to SOPs and GCP.
As a temporary full-time coordinator, you will assist the Clinical Program Manager in administration and execution of clinical trials. Your duties will encompass maintaining procedural documents, fostering communication among clinical teams, and managing study timelines. This is a vital role to streamline operations and enhance trial success.
Key Responsibilities:
• Coordinate compliance with Good Clinical Practices
• Develop and update clinical documents
• Maintain an organized system of SOPs
• Serve as primary contact for study documentation
• Ensure timely supply and equipment readiness
Requirements:
• Relevant bachelor's degree mandatory
• Minimum 2 years of applicable experience
• Research setting experience is a plus
• Proficiency in MS Office applications
• Exceptional communication and problem-solving skills
Leverage your skills in clinical trial management to elevate the efficiency and quality of research activities in this collaborative setting.
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Apply on Kit Job: kitjob.ca/job/2g8vcz
📌 Coordinator for Clinical Trial Operations (Halifax Regional Municipality)
🏢 Nova Scotia Health Authority
📍 Halifax Regional Municipality
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