The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports, case management, and ensuring compliance with regulatory requirements in the healthcare domain.

The Safety Data Lead role at Merck is responsible for analyzing and interpreting adverse experience reports for investigational and marketed products, ensuring compliance with regulatory requirements and internal processes. This involves data entry, case management, and collaboration with stakeholders to resolve issues and optimize processes within the pharmacovigilance domain.

The Safety Data Lead analyzes and interprets adverse experience reports for investigational and marketed products, ensuring compliance with regulatory requirements and internal processes. This role involves data entry, case management, and collaboration with stakeholders to resolve issues and optimize processes within the pharmacovigilance domain.

The Safety Data Lead role at Merck focuses on the analysis, interpretation, and data entry of adverse experience (AE) reports for investigational and marketed products. This position requires compliance with regulatory requirements and internal processes, collaboration with stakeholders to resolve issues, and support for optimizing case management activities. The role operates under the supervision of a GPVCM Manager and involves applying clinical knowledge and understanding of pharmacovigilance processes.

The Safety Data Lead is responsible for analyzing and interpreting adverse experience (AE) reports, managing cases for investigational and marketed products, and collaborating with stakeholders to ensure compliance with regulatory requirements and internal processes within the pharmacovigilance domain.

Associate Director, Launch Excellence role at Merck, focusing on shaping and executing product launches in the pharmaceutical industry. This role translates enterprise priorities into launch strategies, manages cross-functional stakeholders, and drives launch execution to accelerate impact. It involves developing launch frameworks, best practices, and serving as a PMO for priority assets.

The Associate Director, Launch Excellence PMO at Merck will support new launch brands by managing plans, tracking actions, and identifying risks. This role involves cross-functional coordination to ensure readiness and drive execution, with an emphasis on learning and improving launch approaches.

Associate Director, Marketing Excellence role at Merck, focusing on refining brand marketing strategy, enhancing market insights, strengthening data-driven decisions, and improving customer engagement and execution excellence within the pharmaceutical industry. Responsibilities include shaping marketing frameworks, capability building, and piloting new approaches. Requires 8+ years of experience in pharmaceutical strategic marketing or commercial leadership.

This role focuses on translating global medical goals into local strategies and tactics to improve patient outcomes in China within a defined therapeutic area, likely oncology. Responsibilities include building trust with the scientific community, providing medical input to brand strategy and lifecycle management, supporting clinical trials, generating study concepts from local data, and collaborating with internal and external stakeholders. The role also involves reviewing promotional materials and ensuring compliance with local laws and company regulations.

Area Manager for Vaccine Alliance & Customer Engagement in Henan, China. Responsibilities include dealer management, customer engagement, ecosystem building, and ensuring compliance within the vaccine market. Requires 5+ years of experience in the pharmaceutical or sales management, preferably in vaccines.

Area Manager for Vaccine sales and customer engagement in China, focusing on dealer management, customer relationship building, ecosystem development, and ensuring compliance within the pharmaceutical industry.

This role is responsible for driving business growth through product portfolio strategy, identifying strategic opportunities, and fostering cross-functional collaboration within the Pharma and Specialty Business Unit (PSBU). Key duties include performing data analysis, developing performance monitoring dashboards, supporting go-to-market strategies, building financial models for forecasts, and collaborating with stakeholders to monitor performance and streamline processes.

Director of Compliance at Merck in Shanghai, responsible for providing daily compliance consultations, reviewing business activities, managing compliance initiatives and projects, facilitating committee meetings, developing training materials, leading internal investigations, and handling government inquiries. The role requires strong knowledge of pharmaceutical compliance and regulatory affairs.

Manager, Vaccine Health Development role at Merck in Urumuqi, China, focusing on implementing access strategies, developing KDM coverage plans, and managing key projects. Requires field access experience, client management, and cross-team collaboration skills. Experience in the vaccine field and RM/RPM experience are preferred.

Senior Manager for Internal Communications at Merck, focusing on managing and leading key internal communication initiatives like Annual Meetings and townhalls. The role involves creative design, project management, and developing innovative plans for employee engagement while highlighting company strategic priorities. Requires a Bachelor's degree in Communications or Marketing, 10+ years of experience, and strong skills in project planning, execution, copywriting, and stakeholder collaboration.

This role focuses on supporting and facilitating learning and development activities within the FLSL/SLSL commercial and compliance sectors of Merck's pharmaceutical business. The Senior Training Manager will collaborate with business leaders to understand needs, design and execute learning plans, and ensure successful learning outcomes. The role involves consulting, delivery of training, and acting as a liaison between the L&D function and business units to drive desired business results through enhanced capabilities.

Project lead for early clinical research in China for GYN programs, focusing on developing products towards registration, engaging KOLs, and preparing for regulatory submission.

The Safety Data Lead role at Merck focuses on analyzing and interpreting adverse experience (AE) reports for investigational and marketed products, ensuring compliance with regulatory requirements and internal processes within Global Pharmacovigilance Case Management (GPVCM). This role involves data entry, collaboration with stakeholders, and supporting process optimization. It requires a healthcare or life sciences degree and understanding of pharmacovigilance regulations.

Responsible for processing adverse experience (AE) reports with high quality and compliance in the global safety system for investigational and/or marketed products, under the direction and supervision of a Global Pharmacovigilance Case Management Manager. Performs triage, analysis and interpretation of AE data following Company Standard Operating Procedures (SOPs) and guidelines. Supports business processes important to Global Pharmacovigilance Case Management operations and works closely with other staff within the organization as well as cross-functionally.

Manager responsible for ensuring patient safety, high-quality data, and compliance with company requirements and regulations in clinical trials within a specific country. This role involves implementing local/global processes, identifying improvement opportunities, supporting audits and inspections, and overseeing quality control and training activities.