job title: Associate analyst-clinical trial supply(merck)

Your Role:

Successful candidate to join our Global CTS (Clinical Trial Supply) team in delivering exceptional support and services, including Finance, Contracts, eTMF Operations, Database Management, and KPI Management and also will be responsible for managing the day-to-day operations of the Global CTS team, ensuring high-quality support, and driving process improvements.

Who You Are:

Minimum Requirements:

• Postgraduate degree in Life Sciences, Biotechnology, or MPharm.

• Experience: 2 to 7 years.

Preferred Requirements:

• Support the coordination and management of clinical supply projects, including planning, scheduling, budgeting, and resource allocation.

• Archive clinical supply documentation in internal and external GMP and GCP systems.

• Organize and control the compilation of documents for approval by the competent person.

• Check the content and completeness of technical specifications, documents, and contract annexes, and archive them appropriately.

• Manage project documentation, including project plans, status reports, and meeting minutes.

• Create and review supply contracts and control budget/invoice approvals within the defined framework.

• Support post-trial reviews and identify opportunities for process improvement.

• Assist the Clinical Supply Manager and Coordinator with other project-related tasks as required.

• Ensure full GMP compliance and documentation for clinical supply activities, including returns, destruction, and full global traceability of Investigational Medicinal Products.