Safety Data Lead I

Merck Merck · Pharma · Beijing, China

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.

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

  • Clinical Data Management
  • Data Analysis
  • Data Processing
  • Data Quality Assurance
  • English Language
  • Japanese Language
  • Pharmacovigilance
  • Regulatory Requirements

Nice to have

  • Ensure Compliance
  • Internal Processes
  • Time Management

What the JD emphasized

  • regulatory requirements
  • Global Pharmacovigilance Case Management (GPVCM) processes
  • reporting requirements