Global Clinical Supply Planning Lead

Job Description The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full portfolio of clinical trials.• GCS is accountable for the planning, sourcing, labelling,- packaging -and delivery of clinical supplies to clinical sites globally. The GCS Planning (Planning) organization is the key interface between clinical development teams and the operational/executional arms within the business.• • - - This - role works with in the Planning- Execution and Inventory -Management- Section of the GCS Planning organization.-- W orking independ e ntly, the Inventory Manager- Clinical Supplies Project Manager- ( IM- CSPM) - creates - strategic and operational plans associated with- the downstream activities -of- clinical supplies -for their assigned stud ie s . - - The primary function of the -IM CSPM -is planning the- availability- of materials and subsequent movement through our depot network -and further- through to distribution and management of materials- to the -clinical site. - The incumbent must have- demonstrated -understanding of E2E product development process & connectivity between functions supporting pipeline (i.e. clinical development, CMC, supply chain, & human health), and balancing needs of patients & ensuring stable supply of product.- • - - Primary activities include, but are not limited to: - - Participates- on -the- Clinical Trial Team - (CTT) - and- collaborates closely with- other functional area representatives to negotiate timelines and strategy for clinical supplies . - Interacts with- key partner s in both GCS (Logistics and Trade, Distribution, Operations- etc.) as well as - other- organizations such as -G lobal- C linical- T rial- O perations (GCTO) - headquarter -and r egional colleagues and- Global Development Quality -(GDQ) -to address clinical supply related topics. - Responsible and accountable for- establishing -the timelines for clinical•supply•needs•per pro tocol- and- ensuring a robust- signal for packaging - and distribution for- Clinical Finished Goods (CFGs) - Analyzes and- anticipates - clinical study -risks as they relate to clinical supply chain deliverables and prepares, analy ze s, and/or- develops -mitigation strategies for review with clinical partners and senior leaders.- - Responsible and accountable for- utilizing -key - tools /systems - such as IRT & Microsoft PowerApps ,- SWMS, Veeva, MEDS, MyLearning, and other Microsoft Applications -in the management of clinical supplies for assigned studies. - Works directly in the SAP system to- ensure a robust and- consolidated -forecast for- CFGs is maintained .- - - Report- clinical supply chain- incidents to support the gathering of- metrics- in GCS- to describe business health . Participate in- root causing -to- identif y -areas for operational improvement. - Participates in initiation and- timely - processing- of change controls- through collaboration with GCS Planning and other cross functional stakeholders and- in accordance with -established GCS planning SOPs/BPs and QMS Topic 3.4 Change Control Procedures and Work Instructions.- - Participates in- authoring and timely processing of deviation records as well as support s - deviation investigations as required. - Participate s -in critical non-pipeline- and compliance- activities in support of- GCS P lanning (e.g., process improvement initiatives, subject matter expert roles,- SOP/BP development/maintenance,- cross functional projects, etc.) - Participates in -supporting regulatory agency inspections for assigned trials as- required . - Demonstrates high capability to solve unstructured problems, make informed risk decisions considering both technical & business risks, & influence portfolio decisions with facts and data • - Demonstrates ability to balance strategy with ability for tactical execution and has strong ownership & accountability of assigned work • - Focus on Customers & Patients. - Make rapid, disciplined decisions. - Demonstrates Ethics & Integrity. - Required Experience and Skills:- - B achelor's Degree in business , supply chain management, engineering or scientific discipline or- High School Diploma with- 10+ years- equivalent- industry- experience in Pharmaceutical Clinical Supply (packaging, labeling,- logistics -and clinical supply inventory management)- - - At least- 5- year s - of- experience in project management- - At least- 5 -years of experience in planning, scheduling, coordination and processing of supply chain activities, or the equivalent • - Excellent Communication & Interpersonal Skills:- a bility -to effectively communicate with stakeholders at various levels, including cross-functional teams, senior management, external vendors, and clinical sites. Strong negotiation, influencing, and relationship-building skills to ensure alignment and collaboration in the supply planning process. • - Project Management Skills:- s trong -knowledge of the principles of project management and clinical customer relationship management. - Technical Proficiency: f amiliarity with supply chain systems and software ( e.g. -SAP or Oracle) and demand planning principles -as well as Microsoft Excel, PowerPoint, and Word - Strong Analytical &- Problem Solving -Skills: ability to analyze complex data,- identify -trends, and make data-driven decisions to- optimize -supply chain processes. - Flexibility & Adaptability:- Demonstrates -ability to thrive in a fast-paced and dynamic environment, with the capability to adapt quickly to changing business needs and priorities. • - Detail Oriented & Organized:- s trong attention to detail in managing complex supply chain- activities;- ability -to multitask, prioritize tasks, and meet tight deadlines. • - Continuous Improvement Mindset: Proactive approach to- identify -process inefficiencies, develop solutions, and drive continuous improvement initiatives within the clinical supply planning function. - Proficiency -in using supply chain management systems and software, including experience with ERP systems (e.g., SAP), demand planning tools, and inventory management systems. - Proven record in project / portfolio management. - Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP) is highly desirable. - - Preferred Experience and Skills: - - - Results-orientation with the proven ability to execute on collaborative projects and develop subject matter- expertise • • - Knowledge of order management, supply chain- operations -and document control. • - #eligibleforERP GCScareer26 #MSJR Required Skills: Adaptability, Adaptability, Business Risks, Change Management, Clinical Development, Clinical Supplies Management, Clinical Supply Chain Management, Clinical Trial Management, Complex Data Analysis, Cross-Functional Leadership, Data Analysis, Demand Planning, Detail-Oriented, Deviation Investigations, Good Manufacturing Practices (GMP), Interpersonal Relationships, Inventory Management, Key Performance Indicators (KPI), Materials Requirements Planning (MRP), Portfolio Management, Process Improvement Projects, Project Management, Risk Management, Supply Chain Optimization, Supply Chain Systems {+ 2 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.- For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is $117,000.00 - $184,200.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits.- Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at . You can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: -We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: -We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully- Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. -No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.- Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 10% Flexible Work Arrangements: Hybrid Shift: 1st - Day Valid Driving License: Yes Hazardous Material(s): No Job Posting End Date: 06/3/2026 *A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID: R398212 #J-18808-Ljbffr