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Pharmacovigilance Associate

Novotech
NovoTech
0-3 years
Not Disclosed
India
10 April 6, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Associate | Full-Time | India
Experience Required: 0-3 years

Job Description:
We are seeking a dedicated Pharmacovigilance Associate to join our team in India. This role is critical for ensuring the safety and compliance of clinical trials and post-marketing surveillance activities. The ideal candidate will have hands-on experience in safety monitoring and regulatory reporting, along with a strong understanding of pharmacovigilance processes and guidelines.

Key Responsibilities:

  • Monitor and manage the safety aspects of clinical studies and post-marketing surveillance.

  • Handle the safety mailbox, ensuring timely review and follow-up of safety data.

  • Prepare and maintain safety management plans in alignment with study requirements.

  • Set up and manage safety databases for clinical studies.

  • Process and submit Individual Case Safety Reports (ICSRs) including SAEs, SUSARs, and AEs.

  • Ensure compliance with ICH-GCP guidelines, SOPs, and local/global regulatory requirements.

  • Collaborate with cross-functional teams to maintain high-quality safety reporting standards.

Qualifications & Experience:

  • Bachelor’s degree in Life Sciences, Pharmacy, or related field.

  • 0-3 years of experience in pharmacovigilance, drug safety, or clinical research.

  • Knowledge of ICH-GCP, pharmacovigilance SOPs, and regulatory reporting requirements.

  • Strong attention to detail, analytical skills, and ability to manage safety data accurately.

Location: India (flexible across major cities)

Why Join Us:

  • Opportunity to work in a dynamic, global healthcare environment.

  • Exposure to cutting-edge pharmacovigilance practices and regulatory frameworks.

  • Career growth with training and professional development in drug safety.