Be a key player in clinical research with BeOne as a Senior Clinical Study Start-Up Specialist, working remotely from Canada. Drive efficient 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 innovative 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 environments • 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. #J-18808-Ljbffr

📌 Senior Clinical Study Start-Up Specialist (Winnipeg)
🏢 BeiGene
📍 Winnipeg