Study Specialist II – Global Study Operations

Study Specialist II – Global Study Operations (12 Month Contract)

We're currently supporting an exciting opportunity with a leading rare disease biotechnology company for a Study Specialist II to join their Global Study Operations team.

This role will play a key part in supporting the delivery of Phase I-IV and post-approval clinical studies, working closely with Study Managers, CROs, vendors, and cross-functional stakeholders to ensure high-quality study execution.

Key Responsibilities

• Support study planning, execution, and operational delivery activities.
• Contribute to site feasibility, site management, and investigator support.
• Oversee essential study documentation and Trial Master File (TMF) management.
• Support vendor oversight and management, including CROs and specialist vendors.
• Coordinate regulatory document collection and study start-up activities.
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