This role provides high-level administrative support to the VP of International Market Access and their leadership team. Responsibilities include managing complex schedules, calendars, travel, expenses, planning meetings, onboarding new employees, and creating purchase orders. The role also involves monitoring spend vs. budget, supporting departmental initiatives, coordinating special projects, and authoring communications. The ideal candidate has extensive experience as a Senior Administrative Associate, advanced computer skills, and strong attention to detail.

Executive Director, Clinical Data Management Regional Head – Europe, responsible for leading global geographic strategy and performance, translating functional area and GDMS strategic imperatives into region-specific priorities and plans. Partners with GDMS and GCTO leaders to drive global alignment, standardization, and transformation of data-management practices, representing their function and geography network in GDMS LT forums, and ensuring resource excellence, capability growth, and operational readiness worldwide. Requires enterprise-level expertise in GDMS data operations, governance, and digital enablement strategy, with a strong understanding of end-to-end data management processes and systems. Deep knowledge of ICH/GCP guidelines is essential.

The Associate Director, Quality Operations is responsible for ensuring GMP compliance for clinical supply functions at the Werthenstein site. This role involves managing quality activities, supporting compliance-based programs, solving complex problems, improving quality systems, and overseeing SOP management. The position also includes coordinating regulatory inspections, advising on GMP compliance for facilities and equipment, and acting as a Quality representative for manufacturing programs.

Associate Director, Joint Clinical Assessment (JCA) Dossier Content role within Merck's Global Medical & Value Capabilities (GMVC) EMEAC Hub. Responsible for developing and writing product-specific JCA Dossiers in accordance with EU HTAR requirements. This involves engaging with stakeholders, understanding dossier templates and procedures, representing GMVC in dossier generation teams, and ensuring the incorporation of relevant content from cross-functional experts. The role requires close collaboration with Market Access, HTA statistics, regional Medical Affairs, Regulatory, and Global Value & Implementation teams to align dossier content with the value strategy and ensure timely execution of tasks. Key responsibilities include leading the writing of dossiers, assuring timely development of sections, providing input into strategic options, ensuring content availability, communicating with country medical teams, conducting literature searches, staying updated on process rules, ensuring compliance with standards and regulations, and overseeing systematic literature reviews. The role also involves leveraging technical tools and digital solutions to streamline dossier creation and maintenance.

Internship role in Process & Support Operations at Merck, focusing on supporting early-phase clinical therapies manufacturing. Responsibilities include operational support, administrative tasks, data entry, GMP/EHS standards adherence, material handling, and continuous improvement tasks within a manufacturing environment. Requires a Bachelor/Master's degree in a relevant discipline and proficiency in MS Office and German/English.

Associate Director role focused on expanding sustainable access to medicines and vaccines in low- and middle-income countries (L&MICs) through commercially viable models and partnerships. Drives partnership-enabled solutions, pipeline planning, and business development to ensure market reach and long-term growth.

Associate Director, Lead of Laboratory Compliance, Metrology, and Validation for a global analytical organization within a pharmaceutical company's Research Laboratories Division. Responsibilities include managing a team, overseeing GMP documentation and SOPs, handling investigations and change records, driving harmonization of analytical procedures, and supporting audit and inspection activities. Requires experience in pharmaceutical/related industry supporting GMP analytical laboratory testing or QA, in-depth knowledge of regulations, and team leadership experience.

Key Account Manager responsible for end-to-end management of strategically relevant national and international veterinary corporate clients within the Companion Animal Business Unit in Switzerland. Ensures sustainable growth, strong long-term customer partnerships, and consistent implementation of corporate account strategies.