Drug Safety Coding Specialist CLIN BIOSCIENCES
CLIN BIOSCIENCES
Office Location
Full Time
Experience: 2 - 2 years required
Pay: INR 2600000 - INR 3800000 /year
Type: Full Time
Location: Hyderabad
Skills: drug safety, Pharmacovigilance, caseprocessing, clinicalsafety, medicalcodingpv, argussafety, codingspecialist
About CLIN BIOSCIENCES
Job Description
We are seeking an experienced Drug Safety Coding Specialist with a strong background in pharmacovigilance terminology and regulatory coding standards.
Roles and Responsibilities
-
Perform accurate and consistent coding of adverse events, medical history, lab terms, and concomitant medications using MedDRA and WHO-DD.
-
Review and validate terms in Individual Case Safety Reports (ICSRs) to ensure alignment with global PV standards.
-
Perform recoding or dictionary version updates in compliance with regulatory requirements.
-
Collaborate with case processors, medical reviewers, and data management teams to resolve coding discrepancies.
-
Ensure compliance with ICH-GCP, GVP, and internal SOPs.
-
Maintain and update code lists and contribute to coding conventions development.
-
Support training of new team members on dictionary use and coding best practices.
-
Participate in audits, inspections, and quality control checks related to coding.
Qualifications
- B.Pharm / M.Pharm / PharmD / MBBS / BDS / B.Sc. Life Sciences
- MedDRA coding training or pharmacovigilance certification is a plus
- 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