Offer summary
Qualifications:
Bachelor's degree or equivalent experience, 2+ years in clinical trial environment, Knowledge of clinical supply operations, Strong proficiency in Microsoft Office, Excellent written and verbal English skills.
Key responsabilities:
- Support global clinical trials' supply chain
- Develop study-specific plans for projects
- Coordinate internal teams and provide updates
- Ensure compliance with company and regulatory requirements
- Participate in ongoing training for new regulations