Global Clinical Supply Project Lead

MSD Malaysia; West Point (PA); On-site; USD 110,000 - 170,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision care

401(k) retirement plan

Paid holidays

Vacation

Sick leave

Compassionate leave

Job summary

Merck & Co., Inc. is seeking a Protocol Clinical Supplies Project Manager to design strategic plans for clinical supplies across assigned studies. You will serve as the primary GCS contact for internal and external stakeholders and represent GCS at clinical development meetings.

Strong pharma process knowledge and cross-functional collaboration are required. Responsibilities include establishing timelines for supply needs, coordinating with sourcing, manufacturing, and distribution, and driving

Qualifications

• Bachelor’s degree in scientific, business, or related field.
• At least 5 years in project management and in planning/scheduling of supply chain activities.
• Experience communicating with stakeholders across levels and cross-functional teams.
• Familiarity with GMP/GCP and clinical supply documentation.

Responsibilities

• Act as a key stakeholder on Clinical Trial Teams and set timelines.
• Collaborate with regulatory, quality and supply chain teams on topics.
• Establish study-specific timelines and signal for sourcing, manufacturing, packaging, distribution.
• Analyze risks and develop mitigation strategies for review with partners.
• Author clinical supply docs for labeling, packaging, and CMC activities.
• Support IVR system development and UAT for studies.
• Participate in change controls, deviation handling, and process improvements.

Skills

Project Management

Clinical Trial Management

Stakeholder Management

Analytical Thinking

Strategic Planning

Interpersonal Skills

GMP/GCP Knowledge

Education

Bachelor’s Degree in science/business/related

Tools

SAP

Oracle

Excel

PowerPoint

Word

Job description

Merck & Co., Inc. is seeking a Protocol Clinical Supplies Project Manager to design strategic plans for clinical supplies across assigned studies. You will serve as the primary GCS contact for internal and external stakeholders and represent GCS at clinical development meetings.

Strong pharma process knowledge and cross-functional collaboration are required. Responsibilities include establishing timelines for supply needs, coordinating with sourcing, manufacturing, and distribution, and driving