Pharmacovigilance Services Associate – Bengaluru, India
Job Type: Full-Time
Experience Required: 0–2 Years
Job ID: AIOC-S01622133
About the Role
Accenture is seeking a Pharmacovigilance Services Associate to join its Life Sciences R&D vertical in Bengaluru. This role focuses on drug safety surveillance and pharmacovigilance operations, supporting global biopharmaceutical clients in monitoring and assessing the safety of pharmaceutical products.
You will contribute to maintaining patient safety and ensuring compliance with global regulatory requirements, working with clinical trial data, healthcare provider reports, and patient feedback. The role is ideal for early-career professionals with a Pharmacy background who want hands-on exposure to pharmacovigilance case processing, ICSRs, and safety database management.
Key Responsibilities
Perform end-to-end pharmacovigilance operations, including case identification, data entry, MedDRA coding, case processing, submission, and follow-ups in compliance with client-specific and global regulatory guidelines.
Monitor, evaluate, and document adverse drug reactions to ensure patient safety.
Assist in the review and assessment of safety data from multiple sources, including clinical trials, healthcare professionals, and patient reports.
Escalate potential safety issues or delays in timelines to supervisors, ensuring compliance with regulatory requirements.
Work collaboratively within the Pharmacovigilance team while handling individual contributor responsibilities.
Follow detailed and moderate-level instructions for daily tasks and new assignments.
Participate in rotational shifts as required.
Required Qualifications
Educational Qualification: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).
Experience: 0–2 years in pharmacovigilance, drug safety, or related roles.
Strong attention to detail and ability to follow regulatory guidelines.
Good interpersonal and communication skills for effective collaboration with team members and supervisors.
Preferred Skills
Familiarity with global pharmacovigilance regulations (e.g., ICH-GCP, local regulatory requirements).
Knowledge of safety databases and case processing systems is a plus.
Understanding of clinical trials and post-marketing safety surveillance.
Work Location
Bengaluru, India (On-site)
About Accenture
Accenture is a global professional services company with expertise in digital, cloud, and security solutions. With over 784,000 employees across 120+ countries, Accenture delivers strategy, consulting, technology, and operations services, driving innovation and creating value for clients, stakeholders, and communities.
At Accenture, we foster a diverse and inclusive workplace, supporting the holistic well-being of employees and providing opportunities for professional growth through certifications, learning programs, and cross-functional experiences.
Equal Opportunity Employer
All employment decisions are made without regard to age, race, religion, gender, sexual orientation, disability, veteran status, or any other protected category. Accenture actively promotes a bias-free, inclusive, and safe workplace.
Important Notice
Be aware of fraudulent job offers requesting payment for employment. Accenture never asks for payment. If you receive such a request, do not respond and report to india.fc.check@accenture.com.
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