Offer summary
Qualifications:
Bachelor's degree or equivalent qualification, 5+ years experience for PM, 8+ for SrPM, Experience in clinical supplies is preferable, Strong knowledge of Microsoft Office suite, Relevant experience in clinical trial environments.
Key responsabilities:
- Manage full supply chain for global trials
- Develop study specific plans and updates
- Mentor junior team members and guide on projects
- Ensure compliance with company/client requirements
- Participate in process improvement initiatives