Pharmacovigilance Jobs at Accenture | M Pharm Candidates Apply Now
Are you looking to start or grow your career in pharmacovigilance and drug safety surveillance? Accenture is hiring a Pharmacovigilance Services Associate in Bengaluru. This full-time role offers the opportunity to work with one of the world’s leading professional services companies, supporting global biopharma clients in ensuring patient safety, regulatory compliance, and improved outcomes.
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With over 775,000 employees across 120+ countries, we deliver Strategy & Consulting, Technology, Operations, and Accenture Song—powered by advanced technology and intelligent operations centers. We embrace change to create value and shared success for our clients, people, shareholders, partners, and communities. Learn more at www.accenture.com.
Job Details
- Position: Pharmacovigilance Services Associate
- Location: Bengaluru
- Job Type: Full-time
- Job Code: AIOC-S01603794
- Qualifications: Bachelor of Pharmacy or Master of Pharmacy.
- Experience: 1–3 years (0–2 years considered for entry-level applicants).
- Skills: Strong knowledge of pharmacovigilance operations and drug safety surveillance.
About the Role
As a Pharmacovigilance Services Associate, you will be part of Accenture’s Life Sciences R&D vertical. The team supports clinical trials, regulatory services, pharmacovigilance, and patient services solutions for the world’s leading biopharma companies. You will be responsible for case management activities, including case identification, data entry, MedDRA coding, case processing, submissions, and follow-ups for ICSRs in the safety database, ensuring compliance with client guidelines and global regulatory requirements.
Key Responsibilities
- Manage the affiliate mailbox and reconcile reports per process.
- Perform follow-ups for both serious and non-serious cases.
- Create, process, and submit individual case safety reports (ICSRs).
- Ensure accurate MedDRA coding and data entry in safety databases.
- Support drug safety surveillance in alignment with regulatory standards.
- Work in collaboration with the clinical, regulatory, and pharmacovigilance teams.
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