Safety Data Lead I

Merck Merck · Pharma · Beijing, China

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.

What you'd actually do

  1. Performing analysis, interpretation, and data entry of adverse event reports from a wide range of sources and therapeutic areas, demonstrating increasing proficiency in clinical knowledge, Global Pharmacovigilance Case Management (GPVCM) processes and regulatory guidelines.
  2. Providing support or leading operational activities appropriate to level of experience and expertise.
  3. Collaborating with internal and external stakeholders to resolve issues of varying complexity to guarantee process standardization and adherence and ensure compliance with reporting requirements.
  4. Supporting simplification and optimization of case management activities to enhance overall effectiveness.

Skills

Required

  • Case Management
  • Clinical Knowledge
  • Data Processing
  • Data Quality Assurance
  • Pharmacovigilance
  • Process Standardization
  • Regulatory Compliance
  • Regulatory Requirements

Nice to have

  • English Language
  • Ensure Compliance
  • Japanese Language
  • Time Management

What the JD emphasized

  • regulatory requirements
  • compliance