Offer summary
Qualifications:
Bachelor’s Degree in scientific or healthcare discipline, 7+ years in managing studies at pharmaceutical, biotech, or CRO, 3+ years oncology clinical research experience, CRO/vendor oversight on complex studies required, Oncology therapeutic experience required.
Key responsabilities:
- Manage and oversee Legend Biotech pipeline studies.
- Collaborate with cross-functional teams for study operations.
- Develop and manage study timelines and metrics.
- Ensure compliance with regulatory guidelines and SOPs.
- Maintain audit-ready clinical trial documentation.