MedDRA Coder Drug Safety CLIN BIOSCIENCES
CLIN BIOSCIENCES
Office Location
Full Time
Experience: 1 - 1 years required
Pay: INR 2600000 - INR 3800000 /year
Type: Full Time
Location: Noida
Skills: meddra coding, Pharmacovigilance, drug safety, argussafety, codingspecialist, caseprocessing, medicalcodingpv, clinicalsafety
About CLIN BIOSCIENCES
Job Description
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
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Code Adverse Event terms using MedDRA for clinical trials, post-marketing safety reports, and spontaneous reports.
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Ensure consistency and accuracy in medical terminology coding across safety databases.
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Collaborate with safety physicians, case processors, and medical reviewers to ensure appropriate interpretation and classification.
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Maintain knowledge of current MedDRA updates and implement changes into the safety database.
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Perform quality checks and reconciliation of coded data.
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Support regulatory submissions by ensuring properly coded safety data.
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Participate in coding conventions, coding guideline development, and audit preparedness.
Qualifications
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Bachelors degree in Life Sciences, Pharmacy, Nursing, or related field.
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1-3 years of experience in drug safety coding using MedDRA
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Knowledge of global regulatory guidelines.
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Excellent communication and attention to detail.
Interested to apply can share CV or call/WhatsApp to 9342735755