Safety Data Lead I

Merck Merck · Pharma · Beijing, China

The Safety Data Lead is responsible for analyzing and interpreting adverse experience (AE) reports, managing cases for investigational and marketed products, and collaborating with stakeholders to ensure compliance with regulatory requirements and internal 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 Cleaning
  • Clinical Data Management
  • Data Analysis
  • Data Processing
  • Data Quality Assurance
  • Ensure Compliance
  • Pharmacovigilance
  • Regulatory Requirements

Nice to have

  • English Language
  • Japanese Language
  • Process Standardization
  • Time Management

What the JD emphasized

  • compliance with regulatory requirements
  • regulatory requirements