Global Clinical Supplies Program Lead

Merck & Co.; West Point (PA); On-site; USD 85,000 - 120,000; Full time

Job summary

Merck & Co. is offering a unique opportunity for transitioning service members through a 12-week fellowship program in clinical supply management. This role involves overseeing the clinical supply chain for multiple trials, requiring expertise in project management and planning.

Candidates should have a strong background in managing clinical supply activities and demonstrate leadership skills. This is an exciting chance to gain valuable professional experience while contributing to meaningful work in clinical trials.

Qualifications

• At least 8 years of experience in project management.
• At least 3 years of experience in planning, scheduling, coordination, and processing of clinical supply activities.
• Understanding of MRP systems and demand planning principles.
• Demonstrated ability to negotiate and resolve conflicts.

Responsibilities

• Design strategic and operational plans for assigned clinical studies.
• Serve as the primary GCS point of contact for protocols.
• Interact with various organizations to address drug supply related topics.
• Oversee all bulk drug supply management and allocation.

Skills

Project management

Planning and scheduling

Strong communication skills

Time-management

Problem-solving

Microsoft Excel proficiency

Education

Bachelor's degree in a scientific, business, or related discipline

MS/MBA preferred

Tools

SAP

Microsoft Project

Data analytics/visualization software

Job description

Merck & Co. is offering a unique opportunity for transitioning service members through a 12-week fellowship program in clinical supply management. This role involves overseeing the clinical supply chain for multiple trials, requiring expertise in project management and planning.

Candidates should have a strong background in managing clinical supply activities and demonstrate leadership skills. This is an exciting chance to gain valuable professional experience while contributing to meaningful work in clinical trials.