Job Title: Pharmacovigilance Services – New Associate
Job ID: AIOC-S01624360
Employment Type: Full-Time
Experience Required: 0–2 Years
Location: Chennai, India
Industry: Pharmacovigilance | Drug Safety | Life Sciences
We are hiring a Pharmacovigilance Services – New Associate to support drug safety and surveillance activities within the Life Sciences R&D vertical. This entry-level role is ideal for pharmacy and life sciences graduates seeking to build a career in pharmacovigilance and regulatory drug safety operations.
The position focuses on Individual Case Safety Report (ICSR) processing, adverse event reporting, and compliance with global pharmacovigilance regulations. The role operates under defined guidelines and supervision, offering structured learning and hands-on exposure to global drug safety processes.
Perform case identification, intake, and data entry for ICSRs in pharmacovigilance safety databases
Conduct MedDRA coding, case processing, quality checks, and follow-ups in line with client-specific SOPs
Support timely submission of safety cases to global health authorities as per regulatory timelines
Ensure compliance with applicable global pharmacovigilance regulations and client guidelines
Handle routine pharmacovigilance tasks by following established processes and standard operating procedures
Collaborate with team members and supervisors to ensure accurate and timely delivery of assigned work
Maintain documentation and ensure data accuracy, completeness, and consistency
Work in rotational shifts, if required, based on business needs
Bachelor of Pharmacy (B.Pharm)
OR
Bachelor’s Degree in Life Sciences or a related discipline
0 to 2 years of experience in pharmacovigilance, drug safety, or life sciences operations
Freshers with relevant academic exposure or internships in pharmacovigilance are encouraged to apply
Basic understanding of pharmacovigilance and drug safety surveillance concepts
Knowledge of adverse event reporting and ICSR lifecycle is an advantage
Strong attention to detail and accuracy
Ability to follow defined processes and work under supervision
Good communication and documentation skills
Willingness to work in a team-based environment
Flexibility to work in rotational shifts
Accenture is a global professional services organization with strong capabilities in digital, cloud, security, and intelligent operations. Serving clients across more than 120 countries, Accenture supports life sciences organizations across research, clinical development, regulatory affairs, pharmacovigilance, and patient services. With a strong focus on innovation and operational excellence, Accenture enables global biopharma companies to improve patient outcomes and regulatory compliance.
This role provides a strong foundation for long-term growth in pharmacovigilance, drug safety operations, regulatory affairs, and life sciences consulting. Candidates gain exposure to global safety databases, regulatory requirements, and industry best practices.
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