
Director, Global Clinical Supply, Due Diligence and Integration (Hybrid)
Merck
Summary
Global Clinical Supply (GCS) organization within our Company's Research Laboratories is accountable for managing the 'end-to-end' integrated clinical supply chain across our Research & Development Division enabling the execution of all our clinical trials with a #No patient left behind mindset. GCS supports more than 300 Phase I-IV clinical trials run inhouse, 400+ outsourced or run by partners as well as our Company's ISS clinical trials (300+). GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites across more than 60+ countries, all in accordance with US and WW regulations, company policies and Standard operating procedures.
Job description
The Global Clinical Supplies (GCS) Due Diligence and Integration (DDI) Lead plays a critical leadership role in unlocking the value of breakthrough science and advancing our Company's growing portfolio. The Director supports front-end diligence efforts and spearheads the end-to-end clinical supply chain integration of Business Development & Licensing (BD&L) assets. Leading from pre-deal supply chain evaluation through complete business hand-off, the Director operates at the cross-functional intersection of the Integration Management Office (IMO), clinical trial operations, CMC development, regulatory affairs, quality, procurement, and finance. The incumbent provides strategic leadership and end-to-end accountability for the supply chain integration team, ensuring newly acquired assets, strategic alliances, and collaborative portfolios are seamlessly transitioned into standard operations without disruption to business continuity and clinical trial timelines. The Director brings strong business acumen, emotional intelligence, enterprise leadership, and change management capability to shape asset transition strategies, during complex integration lifecycles.
Key Responsibilities
- Represent GCS on Due Diligence teams - synthesize cross-functional inputs (clinical, CMC etc) to define clinical supply chain risk posture, project clinical supply demand and estimate resource/budget requirements.
- Assess impact of BD&L transaction structures (e.g., acquisitions, ring-fence, collaborations etc) to clinical supply chain operational risks, connecting cause and effect, utilizing organizational expertise to implement and influence risk mitigation plans.
- Partner across the E2E supply chain to drive integration strategy and transition into our company's stable operations (business as usual), while ensuring business continuity of ongoing clinical studies.
- Facilitate structured knowledge management from legacy partners to GCS.
- Support strategic talent retention and integration of legacy colleagues into our Company's network.
- Proactively manage stakeholders and escalate risks to GCS and cross-functional leadership and governance.
- Lead GCS leadership reviews for assigned integrations.
- Drive process optimization initiatives and tools to support continuous improvement of asset integration activities.
- Upskill the organization leveraging learnings from integration activities to improve the GCS clinical supply chain and network.
Position Qualifications
Education Minimum Requirement: Bachelor's degree in STEM, Business, or related field.
Required Experience and Skills
- A minimum of 8 years of experience in clinical supply chain, CMC, integration, or clinical roles within the pharmaceutical industry.
- Proven track record of leading complex, cross-functional project teams through planning, execution, and closeout to deliver milestone targets.
- Ability to build trust and support colleagues, utilizing a high degree of emotional intelligence (EQ).
- Acts as a facilitator and mentor empowering others to succeed.
- Strong abilities in Governance and stakeholder management.
- Understands and provides input into decision-making process around investment of time, resources and spend for Global clinical supplies.
- Is comfortable operating in ambiguous environments and delivering high-quality risk assessments with minimal data inputs under tight timelines.
- Exercises prudence and judgement and maintains strict confidentiality while sharing sensitive information.
- Excellent written and verbal communication skills; Ability to digest complex data sets and translate into appropriate executive summary for senior leadership.
Preferred Experience and Skills
- Strategic Planning, demand-supply
- Project management skills / certification
- Prior experience with clinical supply planning, BD&L, trial operations, and/or production operations
Requirements
- Bachelor's degree in STEM, Business, or related field
- A minimum of 8 years of experience in clinical supply chain, CMC, integration, or clinical roles within the pharmaceutical industry
- Proven track record of leading complex, cross-functional project teams through planning, execution, and closeout to deliver milestone targets
- Ability to build trust and support colleagues, utilizing a high degree of emotional intelligence (EQ)
- Acts as a facilitator and mentor empowering others to succeed
- Strong abilities in Governance and stakeholder management
- Understands and provides input into decision-making process around investment of time, resources and spend for Global clinical supplies
- Is comfortable operating in ambiguous environments and delivering high-quality risk assessments with minimal data inputs under tight timelines
- Exercises prudence and judgement and maintains strict confidentiality while sharing sensitive information
- Excellent written and verbal communication skills
- Ability to digest complex data sets and translate into appropriate executive summary for senior leadership
- Strategic Planning, demand-supply
- Project management skills / certification
- Prior experience with clinical supply planning, BD&L, trial operations, and/or production operations
Benefits
- Medical, Dental & Vision
- Retirement benefits
- 401(k)
- Paid holidays
- Vacation
- Compassionate leave
- Sick days
- Annual bonus
- Long-term incentive
Company overview
Merck & Co., Inc., known as Merck in the United States and Canada and MSD (Merck Sharp & Dohme) internationally, is a premier American multinational pharmaceutical company headquartered in Rahway, New Jersey. Founded in 1891 as the U.S. subsidiary of the German Merck Group, the company became independent following World War I and has since grown into one of the world's largest biomedical companies, ranking fourth globally by revenue. Merck operates across three core business segments: pharmaceuticals, vaccines, and animal health products. The company is renowned for its groundbreaking research and development, having brought numerous life-saving medicines to market including Keytruda (pembrolizumab), a leading immunotherapy for cancer treatment that generated $29.5 billion in 2024 revenue, and Gardasil, a revolutionary HPV vaccine. With approximately 75,000 employees worldwide, Merck maintains a robust pipeline of innovative therapies focused on oncology, vaccines, hospital acute care, cardiology, neuroscience, virology, immunology, and diabetes. The company invests heavily in R&D, spending $17.9 billion in 2024 alone, demonstrating its commitment to advancing scientific discovery. Merck's legacy spans over 130 years of bringing hope to humanity through important medicines and vaccines, operating with a purpose to use leading-edge science to save and improve lives globally while fostering an inclusive workforce and responsible business practices.