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 environment.
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.
