Safety Data Coding Executive CLIN BIOSCIENCES

2.0 - 5.0 years

0 - 0 Lacs

hyderabad, noida, united arab emirates

On-site

Roles and Responsibilities: Perform coding of Adverse Events , Medical History, Indications, and Concomitant Medications using MedDRA and WHO Drug Dictionary. Ensure accurate and consistent data entry within global safety databases. Review case narratives and source documents to assign appropriate codes. Maintain compliance with ICH, GVP, and company SOPs. Coordinate with case processors, medical reviewers, and QA teams to resolve coding discrepancies. Stay updated with MedDRA and WHO-DD version updates and apply changes. Participate in coding audits, quality control, and data consistency checks. Support safety signal detection and regulatory queries with coded data. Qualifications: Bachelor...

Posted 3 months ago

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MedDRA Coder Drug Safety CLIN BIOSCIENCES

1.0 - 3.0 years

0 - 0 Lacs

pune, noida, united arab emirates

On-site

We are seeking a highly detail-oriented MedDRA Coder to support our Drug Safety and Pharmacovigilance operations. The ideal candidate will be responsible for the accurate and consistent coding of adverse event terms using MedDR , ensuring compliance with regulatory and quality standards. Roles and Responsibilities Code Adverse Event terms using MedDRA for clinical trials, post-marketing safety reports, and spontaneous reports. Ensure consistency and accuracy in medical terminology coding across safety databases. Collaborate with safety physicians, case processors, and medical reviewers to ensure appropriate interpretation and classification. Maintain knowledge of current MedDRA updates and i...

Posted 3 months ago

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Drug Safety Coding Specialist CLIN BIOSCIENCES

2.0 - 4.0 years

0 - 0 Lacs

pune, noida, united arab emirates

On-site

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. Maintai...

Posted 3 months ago

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