Global Clinical Supply Director: DD&I & Integration

Msd; Pennsylvania; Hybrid; USD 173,000 - 273,000; Full time

Job summary

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, invites a Director to lead Global Clinical Supply Due Diligence and Integration. The role oversees end-to-end integration, risk assessment, and strategic execution across early to late-stage clinical trials, ensuring continuity and compliance.

Hybrid work option in PA/NJ; required 8+ years in clinical supply chain or related fields, with strong leadership, governance, and stakeholder management skills.

Qualifications

• Bachelor's degree in STEM, Business, or related field required.
• Minimum of 8 years of experience in clinical supply chain, CMC, integration, or clinical roles in pharma.
• Experience leading cross-functional project teams to deliver milestones.
• Strong governance and stakeholder management abilities.
• Comfort with ambiguity and delivering high-quality risk assessments with limited data.

Responsibilities

• Lead due diligence and clinical supply chain integration of BD&L assets to ensure seamless, compliant transitions.
• Represent GCS on due diligence teams and define supply chain risk posture, demand, and resource needs.
• Drive integration strategy across E2E supply chain and ensure business continuity of ongoing studies.
• Lead leadership reviews for assigned integrations and drive process optimization for continuous improvement.

Skills

Change Management

Communication

Cross Functional Projects

Cross-Functional Teamwork

Emotional Intelligence

Enterprise Thinking

Project Management

Leadership

Stakeholder Engagement

Supply Chain

Education

Bachelor's degree in STEM, Business, or related field

Job description

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, invites a Director to lead Global Clinical Supply Due Diligence and Integration. The role oversees end-to-end integration, risk assessment, and strategic execution across early to late-stage clinical trials, ensuring continuity and compliance.

Hybrid work option in PA/NJ; required 8+ years in clinical supply chain or related fields, with strong leadership, governance, and stakeholder management skills.