Job Opportunity: Safety Associate (Pharmacovigilance)

Job Summary
IQVIA, a global leader in clinical research and healthcare intelligence, is seeking a detail-oriented and dedicated Safety Associate to join our team in Kochi. This role is an excellent opportunity for professionals with 1–3 years of experience in pharmacovigilance to advance their careers within a dynamic, global environment. You will play a crucial role in maintaining drug safety standards, ensuring data accuracy, and supporting our mission to improve patient outcomes through clinical excellence.

Job Overview

• Role: Safety Associate
• Location: Kochi, India
• Experience Level: 1–3 Years
• Department: Pharmacovigilance / Drug Safety

Responsibilities

As a Safety Associate at IQVIA, you will be an integral part of our drug safety operations. Your daily activities will revolve around the meticulous management of safety data and ensuring full compliance with both internal protocols and global regulatory standards. Your core responsibilities will include:

• Case Processing: Accurately process Individual Case Safety Reports (ICSRs) in accordance with project-specific guidelines.
• Data Evaluation: Review and evaluate adverse event reports to ensure they are complete, consistent, and scientifically accurate.
• Quality Assurance: Perform precise data entry into safety databases and conduct rigorous quality checks to maintain high data integrity.
• Regulatory Compliance: Adhere strictly to established timelines and international pharmacovigilance regulations to ensure the safety and efficacy of medical products.
• Collaboration: Work closely with internal cross-functional teams to manage case follow-ups and resolve discrepancies effectively.
• Documentation: Maintain meticulous records and documentation to ensure all safety reporting meets industry standards and audit readiness.

Requirements

To be successful in this role, you must possess a strong foundation in pharmacology or life sciences, coupled with practical experience in drug safety. We are looking for candidates who meet the following criteria:

• Education: A graduate or postgraduate degree in Pharmacy, Life Sciences, or a related field of study.
• Experience: 1 to 3 years of proven professional experience specifically in the field of Pharmacovigilance or Drug Safety.
• Technical Proficiency: Hands-on experience in end-to-end case processing and familiarity with safety database operations.
• Industry Knowledge: A solid understanding of global pharmacovigilance workflows, case-processing standards, and relevant regulatory requirements.
• Soft Skills: Strong analytical capabilities, excellent attention to detail, and clear communication skills to effectively collaborate within a global team.

Benefits

Joining the IQVIA team offers more than just a job; it provides a platform for professional growth and exposure to international standards. Benefits of this position include:

• Competitive Compensation: An estimated annual salary ranging from ₹3,00,000 to ₹6,00,000, commensurate with experience.
• Global Exposure: The opportunity to work on international pharmacovigilance projects for a world-renowned healthcare leader.
• Professional Development: Access to ongoing learning opportunities and structured career progression paths.
• Work Environment: A collaborative, professional, and diverse workplace that values innovation and employee well-being.

How to Apply

If you are passionate about drug safety and meet the above qualifications, we invite you to take the next step in your career with us.

Please submit your updated resume and a brief cover letter via email to:
Email: [email protected]

Important: Please ensure that you use the subject line “Application for Safety Associate – Kochi” in your email to ensure your application is directed to the appropriate recruitment team. We look forward to reviewing your credentials.