bioLytical is seeking an Associate for Clinical Research in Richmond, BC, on a one-year contract. The role is pivotal in supporting clinical trials and regulatory compliance efforts.

As an Associate, you will work closely with the Chief Scientific Officer to manage the implementation of multiple studies within the product portfolio. Bring your expertise in clinical operations and strong analytical skills to solve logistical challenges within clinical trials.

Key Responsibilities:
• Write and manage trial protocols and related documents
• Analyze data and compile essential clinical documentation
• Ensure study site compliance with set protocols
• Train staff on protocol and documentation requirements
• Conduct meetings and monitor study progress

Requirements:
• Bachelor’s degree in Biological Science or equivalent
• At least 3 years of clinical operations experience
• Familiarity with FDA regulations ...