Study Start Up and Regulatory Affairs Specialist
ErgomedUnited Kingdom only
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The Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise, ensures regulatory compliance, and serves as a key liaison between internal teams, clients, and external stakeholders Accountable for delivery of assigned study start-up and regulatory milestones within defined scope.
Make independent decisions within assigned scope regarding regulatory processes and documentation approaches.
Handles medium-complexity regulatory environments, including multi-country requirements where applicable.
Leads study start-up and regulatory activities for assigned countries or projects of medium complexity, ensuring delivery in line with timelines, quality standards, and regulatory requirements.