Pharmacovigilance Terminology Analyst CLIN BIOSCIENCES
CLIN BIOSCIENCES
Office Location
Full Time
Experience: 3 - 3 years required
Pay: INR 2400000 - INR 3600000 /year
Type: Full Time
Location: Qatar
Skills: Medical Coding, drug safety, Pharmacovigilance, pv case processing, safety database
About CLIN BIOSCIENCES
Job Description
Roles and Responsibilities
- Manage and maintain medical and product coding dictionaries (MedDRA, WHO-DD) used in pharmacovigilance case processing.
- Review and validate coded terms for adverse events (AEs), medical history, concomitant medications, and indications in safety databases (e.g., Argus, ARISg).
- Ensure coding is consistent, accurate, and aligned with global PV standards and sponsor-specific conventions.
- Support MedDRA version upgrades and dictionary migration activities across global safety platforms.
- Work closely with case processors, medical reviewers, and data managers to resolve coding queries and discrepancies.
- Create and maintain coding conventions, SOPs, and coding rulebooks.
- Assist in quality control (QC) audits and prepare for regulatory inspections.
Qualifications
- Bachelors or Masters in Pharmacy, Life Sciences, Biotechnology, or related fields
- 3-6 years of experience in pharmacovigilance or a related field
- Strong analytical and problem-solving skills
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
Interested to apply can share CV or call/whatsapp to 9342735755