Spclst, Clinical Data Mgmt
MSDBeijing, China
Posted January 16, 2026
Full Time
About the Company
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
Job Description
The Safety Data Lead I is 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.
Requirements
- Bachelor’s degree or above in Health Care or job-related disciplines.
- Advanced writing/reading and intermediate speaking/listening Korean & English language skills.
- Productive Communication: Demonstrate an open and respectful communication style that actively acknowledges other's ideas in any circumstance and selecting the correct stakeholders.
- Business & Operations Management: Understand and correlate processes and responsibilities within and between pillars and how they are aligned with GPVCM priorities.
- Regulatory & Compliance Management: Apply compliance requirements knowledge to ensure adherence to regulations.
- Disease Area Knowledge (Sub Competencies): Have knowledge to expand the scope of Case Processing within or across therapeutic area(s)