Jobs at MSD Animal Health Technology Labs

Leads global primary market research procurement within Marketing Procurement, managing a $150M spend category. Develops global sourcing and category strategies, drives transformational procurement initiatives, manages stakeholders and suppliers, oversees sourcing and contracting, delivers savings and performance KPIs, and builds procurement talent and succession plans.

Leads clinical quality management for UK-sponsored clinical trials, ensuring patient safety, data integrity, GCP compliance, audit and inspection readiness. Responsibilities include quality improvement, regulatory and process leadership, quality control visits, site oversight, issue investigations, CAPA management, vendor qualification, and training development. The role serves as a local subject-matter expert, partners with cross-functional and global teams, and uses digital and AI-enabled tools to improve quality oversight and trend analysis.

Leads clinical trial site management and monitoring across assigned protocols, ensuring ICH/GCP, regulatory, data integrity, patient safety, and company compliance. Conducts site selection, validation, initiation, monitoring, and close-out visits; manages documentation, recruitment, performance issues, audits, and inspections. Partners with investigators, vendors, regulatory bodies, and internal teams, maintains CTMS and eTMF records, contributes to process improvement, and mentors junior CRAs. The role requires extensive monitoring experience and approximately 65–75% domestic and international travel.

Leads the development and writing of product-specific EU Joint Clinical Assessment dossiers for pharmaceutical products. Coordinates cross-functional contributors across Medical Affairs, Market Access, Regulatory, statistics, and value teams; ensures accurate, compliant, scientifically robust content aligned with value strategy. Oversees systematic literature reviews, conducts literature searches, manages dossier timelines and templates, supports country communication, and applies digital tools to streamline dossier creation and maintenance.

Provides scientific leadership and technical oversight for external partners conducting small-molecule process chemistry. Leads synthetic route design, route scouting, process optimization, impurity control, scale-up, API delivery, risk mitigation, and technical decision-making. Collaborates across chemistry, engineering, analytical, quality, and external teams; evaluates data and development proposals; supports technology transfer, quality, compliance, continuous improvement, and mentoring.

Supports UK oncology marketing strategy and execution across product lifecycles. Responsibilities include developing omnichannel campaigns, interpreting customer insights, managing content approvals under the ABPI Code, coordinating agencies and cross-functional teams, testing engagement channels, tracking KPIs, and managing campaign budgets.

Supports end-to-end marketing campaign execution across field and digital channels. Coordinates plans, timelines, assets, approvals, compliance, version control, and cross-functional delivery. Partners with digital, brand, medical, compliance, analytics, and agency teams; supports journey setup, publishing, testing, optimization, and performance reporting. Interprets campaign data, identifies improvement opportunities, and applies test-and-learn insights to improve future execution quality.

Leads regional medical-affairs strategy and execution for pulmonary hypertension across EU5 and Canada. Guides country teams, chairs cross-functional regional forums, translates global priorities into regional plans, engages scientific leaders and external stakeholders, organizes advisory events and symposia, supports data-generation studies, reviews investigator-initiated proposals, and manages patient-support, educational, and risk-management programs. Requires recognized pulmonary hypertension expertise and collaboration across commercial, outcomes research, policy, and market access functions.

Manages UK regulatory activities for oncology pharmaceutical products, including regulatory strategy, submissions, marketing authorisation lifecycle maintenance, product information, packaging, compliance, and communication with the MHRA. Advises internal stakeholders on UK and EU regulations, supports product launches and acquisitions, identifies compliance risks, and represents Regulatory Affairs in cross-functional initiatives.

Conduct observational epidemiology and real-world evidence studies supporting infectious disease and vaccine programs. Design protocols, develop analysis plans, analyze large U.S., UK, and European healthcare datasets, interpret findings, and prepare regulatory and scientific materials. Collaborate with clinical, regulatory, safety, statistics, health economics, and commercial teams. Contribute to product safety, risk management, publications, presentations, and advancement of epidemiologic methods, including causal inference and propensity-score approaches.

Leads global digital and AI compliance within the Privacy and Digital Trust Office. Develops AI governance policies, risk assessments, third-party due diligence, incident reporting, and technical controls for agentic AI. Advises business and technical stakeholders on responsible AI adoption, data protection, emerging regulations, and risk mitigation. Translates legal requirements into operational guidance, monitors regulatory developments, represents compliance on governance committees, and builds cross-functional partnerships across a global organization.