6-month contract — Global Study Operations (GSO)
A global leader in rare genetic disease therapeutics is seeking a Global Study Specialist II to join their Global Study Operations team on a 6-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 Study Specialist II, 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!