Safety Data Lead I

Merck Merck · Pharma · Beijing, China

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.

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 Data Cleaning
  • Clinical Knowledge
  • Data Processing
  • Pharmacovigilance
  • Process Standardization
  • Regulatory Compliance
  • Regulatory Requirements

Nice to have

  • English Language
  • Ensure Compliance
  • Time Management

What the JD emphasized

  • regulatory requirements
  • compliance