Safety Data Lead I

Merck Merck · Pharma · Beijing, China

The Safety Data Lead role at Merck is responsible for analyzing and interpreting adverse experience reports, managing cases for investigational and marketed products, and collaborating with stakeholders to ensure compliance with regulatory requirements and internal processes. This role focuses on data entry, analysis, and process optimization within pharmacovigilance.

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
  • Pharmacovigilance
  • Regulatory Compliance
  • Regulatory Requirements
  • Safety Management

Nice to have

  • Adverse Drug Reactions
  • English Language
  • Ensure Compliance

What the JD emphasized

  • regulatory requirements
  • compliance