Study Delivery Senior Associate

About the Role The Study Delivery Senior Associate provides essential global study management support to clinical study teams, ensuring timely, high-quality, and compliant study execution. They partner with Study Managers to deliver start-up and conduct activities, own specific study tasks and support risk monitoring and issue management, escalating early warning signals with proposed solutions to relevant stakeholders. The Study Delivery Senior Associate will be assigned to individual study teams and specialize in processes supporting many study teams throughout their study lifecycle, enabling opportunities to gain varied experience in study management. What You'll Do

• Lead the development and maintenance of study-level trackers, dashboards, timelines, and tools (e.g., vendor management, sample tracking, drug supply planning) to ensure accuracy and visibility.
• Coordinate logistics for investigator meetings, trial events, and site communications.
• Manage assigned start-up activities, including system setup, access management, and document readiness, ensuring completion to required standards.
• Use study dashboards and reports to monitor global enrollment, data flow, and quality indicators, taking proactive action to address deviations and risks.
• Lead delivery of assigned risk and quality management activities
• Track and report study progress, coordinating with Study team and vendors to resolve operational issues and maintain compliance.
• Deliver assigned components of global recruitment and retention strategies to help ensure enrollment targets are achieved.
• Manage Study Training system activities and oversight
• Build and maintain effective relationships with internal study team members, vendors and investigator sites
• Act as a point of contact for routine study updates, ensuring stakeholders are informed and aligned.
• Identify, prioritize, and escalate risks effectively to support swift, informed decisions.
• Lead vendors and supplier set-up to ensure quality, speed, and consistency in deliverables.
• Maintain and monitor clinical trial systems (e.g., CTMS). What We're Looking For
• Experience in global study management, including start-up, conduct, risk and quality management, and issue escalation.
• Ability to use study dashboards and reports to monitor enrollment, data flow, and quality indicators; proactive risk mitigation.
• Strong coordination and communication skills to manage logistics and vendor/site interactions.
• Familiarity with CTMS and other clinical trial systems; focus on data integrity and compliance.
• Ability to build and maintain relationships with internal study teams, vendors and investigator sites.
• Strong problem-solving skills and the ability to prioritize and escalate risks appropriately.