Senior Study Specialist
SSS_4300719699
Posted: 15/09/2025
- London Area, United Kingdom (Hybrid)
- Contract
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:
- Lead or assist in site and vendor oversight
- Help develop study documentation and training materials
- Manage regulatory documents and ensure compliance
- Track investigator payments and clinical trial insurance
- Support study startup, site management, and risk mitigation
- Facilitate internal and external meeting coordination
- Maintain essential study documents and trial master files
- Collaborate with cross-functional teams and represent GSO in meetings
Who You Are:
- Proactive, agile, and collaborative
- Experienced in study execution, compliance, and vendor oversight
- Knowledgeable in drug development and therapeutic areas
- Detail-oriented with strong communication skills
Qualifications:
- BSc or higher in nursing, life, or health sciences preferred (or equivalent experience)
- Experience managing external vendors (CROs, labs, imaging)
Ready to help transform rare disease care?
Apply now and be part of a team that truly makes a difference!
Sashmika Sakthi
Senior Candidate Consultant
