Clinical Trial Material Manager

Purpose and Scope :

Responsible for planning, coordinating, and managing clinical trial material (CTM) activities for various global clinical supply programs. Monitors inventory and evaluates trends. Summarizes and presents information to teams and management and readily coaches others using expertise. Lends experience for the betterment of the department and manages complex supply chain issues.

Responsibilities and Accountabilities :

• Attends clinical study team meetings and proactively develops packaging and labelling solutions and documentation to support the lifecycle of clinical studies for multiple complex programs with a low level of oversight.
• Produces detailed plans including budgets, forecasts, and timelines, and is responsible for ensuring timelines are met. Executes on compound / drug related supply chain activities including packaging, labelling, and distribution documentation with first-pass quality.
• Plans and monitors packaging and distribution activities and provides input and solutions for
• continual improvement and implements suggested improvements. .
• Establishes and closely monitors project budgetary spend and looks for areas of cost optimization.
• Supports staff development through coaching on process knowledge. Serves as a consultative resource in review of staff documentation and provides instruction for improvement.
• Responsible for implementing departmental solutions and may lead efforts to implement new processes.
• Represents function on cross-functional improvement teams and communicates progress to
• staff on regular basis.

Required Qualifications :

Preferred Qualifications :