Sr Study Operations Specialist

We are hiring a Senior Study Specialist (SS) to join a Global Study Operations team.

Is this the role you are looking for If so read on for more details, and make sure to apply today.

In this role, you will support and/or lead key clinical study activities including site oversight, vendor management, TMF maintenance, and cross-functional study execution. You will work with increasing independence to ensure study quality, timelines, compliance, and budget adherence.

Key Responsibilities

• Support study setup, documentation, and feasibility/site selection activities
• Oversee CRO deliverables including IRB/EC submissions and approvals
• Manage essential study documents and TMF compliance
• Support investigator training, meetings, and updates
• Coordinate vendor oversight, budgets, and clinical trial insurance
• Contribute to risk identification and cross-functional study meetings

Requirements

• BA/BS (life sciences, nursing, health-related field xwzovoh preferred) or equivalent experience
• Clinical research/pharma/biotech experience required
• Experience with CRO/vendor oversight and budget/SOW management
• Strong understanding of clinical trial operations and compliance

If this sounds like a fit, apply now.