Spclst, Clinical Data Mgmt

Merck Sharp & Dohme Corp

Case processing responsibilities
Adverse experience report handling
Global pharmacovigilance sop adherence
The Safety Data Lead I is responsible for processing adverse experience reports with high quality and compliance in the global safety system

Job Summary

  • The Safety Data Lead I is responsible for processing adverse experience reports with high quality and compliance in the global safety system.
  • This role requires independently meeting Key Performance Indicators while serving as a point of contact for resources and guidelines.
  • The position involves assisting with root cause analysis and implementing action plans to ensure regulatory adherence.

Matching Summary

The Safety Data Lead I is responsible for processing adverse experience reports with high quality and compliance in the global safety system.

Skills & Requirements

Must-have

  • Case Processing responsibilities
  • Adverse Experience report handling
  • Global Pharmacovigilance SOP adherence

Nice-to-have

  • Root cause analysis assistance
  • Cross-functional collaboration skills
  • Therapeutic area knowledge expansion

Key Requirements

  • Bachelor's degree in Health Care or related discipline
  • Advanced Korean and English writing/reading skills
  • Intermediate Korean and English speaking/listening skills

Work Rights

Not specified

Tailored Resume

Cover Letter