Job Description
12-month contracted role — Global Study Operations (GSO)
A global leader in rare genetic disease therapeutics is seeking a Senior Study Specialist to join their Global Study Operations team on a 12-month contract. This role supports the successful execution of clinical studies by overseeing site monitoring, vendor management, and study documentation to ensure timely delivery and high-quality data.
About the Role:
As a Senior Study Specialist, you’ll be at the heart of our clinical trials—helping to oversee site monitoring, vendor management, and study execution from Phase 1 through post-approval. You’ll support the team to ensure smooth operations, quality data, and timely delivery, directly contributing to advancing life-changing treatments.
What You’ll Do:
1. Lead or assist in site and vendor oversight
2. Help develop study documentation and training materials
3. Manage regulatory documents and ensure compliance
4. Track investigator payments and clinical trial insurance
5. Support study startup, site management, and risk mitigation
6. Facilitate internal and external meeting coordination
7. Maintain essential study documents and trial master files
8. Collaborate with cross-functional teams and represent GSO in meetin...