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Global Clinical Supply Regions Head (Hybrid)

Posted 30 Aug 2025
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Work experience
10 to 20 years
Full-time / part-time
Full-time
Job function
Salary
$169,700 - $267,200 per year
Degree level
Required language
English (Fluent)
Deadline
8 September 2025

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Lead Strategic Operations for Global Clinical Supply Regions

Job Description

The Global Clinical Supply Regions Head is responsible for providing strategic input, oversight and operational leadership to the activities of GCS in the regions and countries to support the execution of our company's clinical trials (300+ studies) portfolio globally across more than 60 countries. Special attention is needed to the cross functional collaboration between Global Clinical Supply (GCS) and Global Clinical Trial Operations (GCTO) team in conducting our company's clinical trials.

Major Activities and Responsibilities:

  • Active member of GCS Logistics and Regions Leadership team, ensuring customer and key stakeholder focus in GCS core activities
  • Managing the group of Regional leads (P5 and P4) in the different regions, providing leadership and managing performance and ensuring talent hiring, development and retention
  • Establish the appropriate communication channels & decision-making processes between GCS and GCTO, including engagement with Clinical and Regulatory Organizations - communication channels
  • Monitor all Clinical Protocols being supported by GCS to enable the distribution of supplies in the regions through effective collaboration, communication and distribution plans with the other functions in GCS
  • Pro-actively identify potential issues that could interfere with the delivery and utilization of supplies and collaborate in the resolution of issues and/or opportunities for operational improvements
  • Develop global strategies around distribution needed to continuously improve compliance, capabilities and efficiencies in the delivery of Clinical Supplies
  • Lead the implementation and operational adoption of Global Distribution Strategies with the regions, providing effective feedback to Global Clinical Supply as well as support & training to Global Clinical Trial Operations
  • Lead the development and implementation of strategic process improvement initiatives that will continuously improve business performance with a particular focus on the efficiency & effectiveness of our company's Clinical Supply Chain
  • Support the roll out of global practices and processes

Education and Skills Required:

  • Bachelors required (Masters preferred) with at least 10 years’ experience in clinical supplies or clinical trials
  • Demonstrated ability to understand and navigate the nuances of international clinical supplies distribution
  • Demonstrated ability to understand and operate in cultural diverse situations.
  • Demonstrated leadership skills including excellent ability to lead in a matrix environment and in a highly effective collaborative way
  • Demonstrated success in leading project teams or partners to achieve results; line management experience is a plus but not required.
  • Excellent communication skills with the ability to engage confidently and persuasively with senior leadership, influencing decision-making and outcomes
  • Demonstrates a strong sense of urgency and proactive approach to problem resolution
  • Understanding of regulatory frameworks in Clinical trials or clinical supplies, GCP, GDP & GMP, trade compliance

Required Skills: Budget Development, Clinical Information Systems, Clinical Supply Chain Management, Clinical Testing, Clinical Trials Logistics, Communication, Communication Management, Communication Methods, Customer Due Diligence (CDD), Customer Satisfaction, Customer Value Management, Distribution Management, Feasibility Studies, Management Process, Multitasking, People Leadership, Performance Monitoring, Process Improvement Projects, Process Improvements, Risk Management, Site Initiation, Status Reporting, Strategic Thinking, Subcontract Management

Preferred Skills:

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.

Employee Status: Regular

Travel Requirements: 25%

Flexible Work Arrangements: Hybrid

Shift: 1st - Day

Hazardous Material(s): n/a

MSD als werkgever
Keer op keer nieuwe uitdagingen aangaan, dat is wat bij je moet passen als je bij MSD aan de slag wilt. Want continu verbeteren is een van onze drijfveren. Dat geldt zowel voor werkprocessen als voor medewerkers. Gedrevenheid, teamwork en eigen initiatief zijn van groot belang. Bij MSD kun je je op allerlei manieren ontwikkelen. In de…


MSD als werkgever
Keer op keer nieuwe uitdagingen aangaan, dat is wat bij je moet passen als je bij MSD aan de slag wilt. Want continu verbeteren is een van onze drijfveren. Dat geldt zowel voor werkprocessen als voor medewerkers. Gedrevenheid, teamwork en eigen initiatief zijn van groot belang. Bij MSD kun je je op allerlei manieren ontwikkelen. In de diepte, door je te specialiseren in je vak. Maar ook door jezelf te verbreden en door te groeien naar een leidinggevende functie. Internationaal of juist heel lokaal, er zijn talloze andere mogelijkheden om stappen te zetten in je loopbaan, te rouleren in functies of te groeien in je functie. Werken bij MSD is werken in een dynamische high tech omgeving van internationale allure, die toch sterk lokaal geworteld is in Oss, Haarlem en Boxmeer.

Pharmaceutical
Haarlem
5,600 employees