About the Role
As junior MedDRA Coders to support pharmacovigilance operations for global clinical trials and post-marketing safety activities. This role is ideal for professionals with hands-on AE coding experience who are looking to grow in a regulated, global environment.
Key Responsibilities
Perform Adverse Event (AE) coding using the latest MedDRA dictionary
Apply Standard MedDRA Queries (SMQs) accurately
Ensure consistency and compliance with SOPs, MedDRA conventions, and regulatory guidelines
Support data cleaning, query resolution, and reconciliation activities
Collaborate with PV, clinical, and data management teams
Requirements
2–5 years of experience in MedDRA coding
Strong understanding of AE/SAE coding workflows
Familiarity with ICH, GCP, and global PV regulations
Experience working with safety databases (Argus, ArisG, or equivalent) is a plus
Attention to detail and strong documentation skills