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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Associate Director - Triage and Medical Review

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeHyderabad, Telangana, IndiaNo salary listed

About the Job

Requirements

  • MD or MBBS with active Indian registration or eligibility.
  • 10 or more years of industry experience, including 7 or more years in pharmacovigilance.
  • Hands-on experience with Individual Case Safety Report review, narrative authoring, causality assessment, expectedness determination, and MedDRA coding.
  • Expert knowledge of ICH E2A, E2B, and E2D, as well as FDA and EMA pharmacovigilance regulations.
  • Proficiency with Argus Safety or equivalent safety databases.
  • Strong clinical judgment and the ability to provide clear written rationale.

Responsibilities

  • Oversee Individual Case Safety Report medical review and accurate data capture in Argus.
  • Lead triage harmonization and end-to-end case quality across the India POD.
  • Review narratives, author analyses, and develop causality rationales and reporting decisions.
  • Guide expectedness determinations against programmes, products, and approved labeling.
  • Oversee clinically appropriate MedDRA coding for adverse events and medical history.
  • Partner with pharmacovigilance, risk management, and clinical teams before regulatory submissions.
  • Support compounds, resolve case issues, develop standard operating procedures, improve processes, and prepare for inspections.
  • Explore artificial intelligence technologies to strengthen pharmacovigilance activities.

Desired Qualifications

  • Global development or marketed product experience is preferred.
  • GPS POD or insourced pharmacovigilance experience is advantageous.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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