Protocol CSPM: Clinical Trial Supply Leader

Merck & Co.; Rahway (NJ); Hybrid; USD 117,000 - 184,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Benefits package

Job summary

Merck is seeking a Protocol Clinical Supplies Project Manager (CSPM) to design strategic and operational plans for clinical supplies across assigned studies. You will be the primary GCS contact to internal and external stakeholders and will present at Clinical Trial Teams and product-development meetings.

You will balance E2E product development needs with patient-centric supply stability, collaborating with clinical development, regulatory, quality, and other supply chain areas, while

Qualifications

• Bachelor's degree in scientific, business, or related field.
• 5+ years of project management experience.
• 5+ years planning and coordination of supply chain activities.
• Excellent communication and negotiation skills.

Responsibilities

• Serve as primary GCS contact for assigned studies and stakeholders.
• Develop timelines for clinical-supply needs per study and coordinate sourcing, manufacturing, packaging, and distribution.
• Support change controls and deviation investigations as required.
• Prepare clinical supply documentation and participate in Investigator Meetings.

Skills

Analytical Thinking

Clinical Supplies Management

Clinical Supply Chain Management

Clinical Trial Management

Data Analysis

MRP

Project Management

Stakeholder Management

Strategic Planning

Supply Chain

Education

Bachelor's Degree in scientific, business, or related discipline

Tools

SAP

Oracle

Excel

PowerPoint

Word

Job description

Merck is seeking a Protocol Clinical Supplies Project Manager (CSPM) to design strategic and operational plans for clinical supplies across assigned studies. You will be the primary GCS contact to internal and external stakeholders and will present at Clinical Trial Teams and product-development meetings.

You will balance E2E product development needs with patient-centric supply stability, collaborating with clinical development, regulatory, quality, and other supply chain areas, while