Offer summary
Qualifications:
Bachelor's degree or equivalent qualification, 2+ years experience in clinical trials environment, Effective written and verbal communication skills, Strong Microsoft Office suite knowledge, Basic understanding of clinical supply operations.
Key responsabilities:
- Support supply chain for global clinical trials
- Develop study specific plans for assigned projects
- Coordinate efforts with internal teams and update project reports
- Ensure compliance with GxP requirements
- Participate in ongoing training on new regulations