As a Study Start Up Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
**What you will be doing**:- Manages start-up activities for assigned studies at the regional level including supporting site identification/site recruitment/site selection, central and local submissions, site contracts, essential document preparation, Investigational Product (IP) release, site initiation visits (SIVs) readiness, and overall regional site activation readiness to ensure deliverables meet quality and regulatory requirements, project timelines, budget, and sponsor expectations.
- Ensures that clinical delivery project team members and any other cross-functional team members needed to support regional site activations understand responsibilities and performance standards.Reviews metrics and other information sources to monitor team and individual performance, providing feedback to individual and functional...