Job Opportunity: Safety Associate at IQVIA, Kochi

Job Summary

IQVIA, a global leader in clinical research and healthcare analytics, is currently seeking a detail-oriented and motivated Safety Associate to join our Pharmacovigilance team in Kochi. This role is designed for professionals with 1–3 years of experience in drug safety who are eager to advance their careers within a fast-paced, international CRO environment. The successful candidate will play a vital role in ensuring patient safety by managing end-to-end case processing and maintaining rigorous compliance with global regulatory standards.

Responsibilities

As a Safety Associate at IQVIA, your core responsibilities will include:

• Case Processing: Manage the end-to-end processing of Individual Case Safety Reports (ICSRs), including intake, triage, and comprehensive data entry.
• Adverse Event Management: Accurately handle and report both serious and non-serious adverse events in accordance with project-specific timelines.
• Medical Coding: Apply medical terminology and coding standards using MedDRA and WHO-DD to ensure accurate documentation of safety data.
• Regulatory Compliance: Ensure all activities strictly adhere to global pharmacovigilance regulations, including ICH guidelines and Good Pharmacovigilance Practices (GVP).
• Quality Assurance: Conduct thorough quality checks on processed cases and perform follow-up activities to obtain necessary information for case completion.
• Database Management: Maintain high levels of accuracy and efficiency while working within safety database systems (such as Argus or ArisG).
• Collaboration: Work effectively with internal stakeholders and cross-functional teams to resolve case-related queries and ensure seamless operational workflows.

Qualifications & Requirements

To be successful in this role, candidates should possess the following qualifications:

• Education: A degree in B.Pharm, M.Pharm, Pharm.D, or a Life Sciences-related field.
• Experience: 1–3 years of hands-on experience in pharmacovigilance or drug safety operations.
• Technical Expertise: Proficiency in ICSR case processing, medical coding, and navigating PV workflows.
• Regulatory Knowledge: A solid understanding of global regulatory compliance and safety reporting requirements.
• Skills: Exceptional attention to detail, strong analytical capabilities, and effective written and verbal communication skills.
• Systems: Previous experience with safety databases is highly preferred.

Why Join IQVIA?

Joining IQVIA means becoming part of a world-renowned organization at the forefront of clinical research. We offer:

• Global Exposure: The opportunity to work with international safety databases and engage with diverse regulatory frameworks across multiple geographies.
• Professional Growth: A clear pathway for career development in the specialized field of drug safety and clinical research.
• Collaborative Culture: A professional and supportive work environment that values teamwork and innovation.
• Meaningful Work: The chance to contribute to global clinical safety projects that directly impact patient health and medical advancement.

Salary & Benefits

• Compensation: Competitive salary package ranging from ₹3.5 LPA to ₹6.5 LPA, commensurate with your experience and skill set.
• Development: Access to industry-leading training and development programs designed to sharpen your expertise in pharmacovigilance.

How to Apply

We invite qualified candidates to submit their applications for this position. To apply, please forward your updated CV to the following email address:

• Email: [email protected]

Application Tip: To ensure your application receives the appropriate attention, please use the following subject line in your email: “Application for Safety Associate – Kochi”.

IQVIA is an equal opportunity employer committed to creating a diverse and inclusive workplace. We look forward to reviewing your application.