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 setting.

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.
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📌 Oximio Project Specialist in Pharma (Manitoba)
🏢 Oximio
📍 Manitoba