Enhance your career with Oximio as a Project Specialist in clinical trial management, focusing on compliance and operational execution. Play a vital role in pharmaceutical research.

Oximio is on the lookout for a Project Specialist to support its clinical trial projects effectively. This role requires 1-3 years of experience in project coordination or a related life sciences environment. You will work in close collaboration with various teams, ensuring project milestones are met while maintaining compliance with regulatory standards in a GMP workplace.

Key Responsibilities: • Coordinate clinical trial project activities effectively • Support packaging, labeling, and shipping operations • Maintain detailed documentation on procedures • Assist with audit preparation and compliance checks • Train junior staff in packaging processes

Requirements: • Bachelor's degree or equivalent education • Familiarity with GMP and quality assurance processes • Strong organizational and detail-oriented skills • Proficient in MS Office tools • Ability to handle multiple tasks and priorities

Become an integral part of Oximio’s mission to improve patient outcomes through effective clinical research processes.

📌 Oximio Project Specialist in Pharma (Winnipeg)
🏢 Oximio
📍 Winnipeg