Be a key player in clinical research with BeOne as a Senior Clinical Study Start-Up Specialist, working remotely from Canada. Drive productive study start-up processes while ensuring compliance with industry regulations.

In this essential full-time role, your responsibilities will span across managing study submissions and enhancing site activation timelines. You will utilize your 3+ years of experience in clinical operations, leveraging ICH/GCP knowledge and improving workflows. Your efforts directly contribute to the ongoing fight against cancer through creative research solutions.

Key Responsibilities:
• Coordinate study start-up processes and site selection
• Drive rapid completion of tasks from selection through activation




• Manage document preparation for central IRB submission
• Ensure accurate data entry and filing in CTMS and eTMF
• Assist in optimizing local workflows for better outputs

Requirements:
• Bachelor's degree or higher in a scientific field
• Minimum 3 years in clinical research settings
• Understanding of ICH/GCP and country regulations
• Strong ability in document management and negotiation
• Experience in biotech, pharmaceutical, or CRO settings

Empower clinical trials with your expertise at BeOne.
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📌 Senior Clinical Study Start Up Specialist Manitoba
🏢 BeiGene
📍 Manitoba