Associate, Clinical Research (1 year Contract)
Richmond, BC

Overview

This one-year contract position supports in-house clinical operations and assists in the development and implementation of multiple studies for bioLytical’s product portfolio. The role collaborates closely with the Chief Scientific Officer and addresses logistical challenges, resolves issues related to clinical trials, and ensures compliance with regulatory requirements.

Key Responsibilities

• Integrate product knowledge to design, write, and manage trial protocols and study documentation, including ethics applications.
• Conduct data analysis and compile scientific, regulatory, and research documents.
• Ensure study sites and activities adhere to industry protocols and study terms.
• Train and oversee site staff on product tests, protocol requirements, source documentation, and case report form completion.
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