Job Title: Manager – Pharmacovigilance
Job ID: JREQ134114
Posted Date: November 5, 2025
Locations: Bangalore, Karnataka, India | Noida, Uttar Pradesh, India
Industry: Life Sciences & Healthcare
Work Mode: Hybrid (Remote + On-site)
About the Role
The Manager – Pharmacovigilance will lead and oversee pharmacovigilance activities, including biomedical literature monitoring, adverse event assessment, and data management. This role requires a strong understanding of drug safety regulations, medical terminology, and literature review methodologies to ensure high-quality, compliant deliverables across therapeutic areas.
Key Responsibilities
Leadership & Strategy
Establish and maintain best practices and SOPs for literature screening activities, ensuring full compliance with regulatory standards (e.g., ICH, GVP, FDA, EMA).
Oversee all aspects of literature search and screening, including strategy development, process management, and data extraction.
Ensure accuracy, consistency, and regulatory compliance in literature-based adverse event identification and reporting.
Set clear goals aligned with departmental and organizational objectives.
Lead, mentor, and develop a high-performing pharmacovigilance team, providing regular feedback and career guidance.
Collaboration & Communication
Communicate key findings effectively with internal and external stakeholders.
Collaborate with cross-functional teams (e.g., medical writing, regulatory, risk management) to support safety updates, signal detection, and risk mitigation.
Contribute to continuous improvement initiatives across global pharmacovigilance operations.
Training & Quality Oversight
Develop and implement comprehensive training programs for new hires and existing team members.
Evaluate trainee performance and maintain audit-ready training documentation.
Promote adherence to SOPs, policies, and quality assurance standards in all team activities.
About You
Education
Bachelor’s degree (or equivalent) in Pharmacy, Life Sciences, Nursing, or related health science field.
Experience
Minimum 7 years of relevant experience in Pharmacovigilance or Drug Safety.
Proven expertise with biomedical literature databases (e.g., PubMed, Embase) for adverse event identification.
Prior experience managing pharmacovigilance operations, literature review, and safety case assessment.
Skills
Excellent command of biomedical and pharmacological terminology.
Strong writing skills to prepare accurate, concise summaries and reports.
Effective time management and multitasking abilities.
Exceptional English communication skills (written and verbal).
Strong organizational and leadership abilities.
Proficiency in Microsoft Office Suite and database tools.
Certification in Medical Writing or Pharmacovigilance (preferred).
About the Team
The Pharmacovigilance Team at Clarivate provides end-to-end safety services to multiple global clients across all therapeutic areas. The team fosters a supportive, growth-oriented environment, offering:
Personalized training and mentorship.
Opportunities to explore various aspects of pharmacovigilance and client engagement.
Exposure to international projects and compliance systems.
Working Hours
Location: India (Bangalore or Noida)
Shifts: 9:00 AM – 6:00 PM IST or 11:00 AM – 8:00 PM IST
Work Mode: Hybrid (Monday to Friday)
Equal Opportunity Statement
Clarivate is committed to providing equal employment opportunities to all qualified individuals. We ensure non-discriminatory practices in hiring, promotion, compensation, and training, in full compliance with all applicable employment laws and regulations.
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