Pharmacovigilance Services Associate
Location: Bengaluru, India
Job Type: Full Time
Experience Required: 0–2 Years (Up to 3 Years Considered)
Job ID: AIOC-S01619343
Industry: Pharmacovigilance | Drug Safety | Life Sciences
Job Overview
Accenture is hiring a Pharmacovigilance Services Associate to support global drug safety and surveillance operations within its Life Sciences R&D vertical. This role is ideal for early-career professionals seeking hands-on exposure to end-to-end pharmacovigilance operations while working with leading global biopharmaceutical organizations.
As part of Accenture’s Pharmacovigilance & Drug Safety Surveillance team, you will contribute to the monitoring, assessment, and reporting of adverse drug reactions, ensuring patient safety and compliance with global regulatory requirements.
Key Responsibilities
Perform end-to-end Individual Case Safety Report (ICSR) processing in accordance with global regulatory standards
Support case identification, triage, data entry, MedDRA coding, medical review coordination, and follow-up activities
Ensure timely submission of safety reports to regulatory authorities as per client and compliance guidelines
Review and assess adverse event data from clinical trials, healthcare professionals, and consumers
Maintain high data quality and accuracy within the safety database
Adhere to SOPs, work instructions, and applicable global pharmacovigilance regulations
Collaborate with team members and supervisors to resolve routine operational issues
Work as an individual contributor within a structured, team-based environment
Participate in rotational shifts, as required by business operations
Required Qualifications
MSc, BPharm, or MPharm from a recognized institution
0–2 years of experience in Pharmacovigilance, Drug Safety, or Clinical Safety Operations
Candidates with up to 3 years of relevant experience may also be considered
Basic understanding of pharmacovigilance regulations and safety reporting processes
Skills and Competencies
Foundational knowledge of pharmacovigilance operations and drug safety surveillance
Familiarity with ICSR processing workflows and MedDRA terminology
Strong attention to detail and data accuracy
Good written and verbal communication skills
Ability to follow structured guidelines and work instructions
Willingness to learn and adapt in a regulated, fast-paced environment
Strong sense of responsibility toward patient safety and compliance
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With unmatched experience across more than 40 industries, Accenture delivers Strategy & Consulting, Technology, and Operations services, powered by the world’s largest network of Advanced Technology and Intelligent Operations centers.
With a workforce of over 699,000 professionals serving clients in more than 120 countries, Accenture partners with leading life sciences organizations to drive innovation, improve patient outcomes, and accelerate scientific progress.
Why Join Accenture?
Work with globally recognized biopharmaceutical clients
Gain exposure to real-world pharmacovigilance and regulatory operations
Build a strong foundation in drug safety and life sciences R&D
Access structured training, career development pathways, and global best practices
Be part of an organization committed to innovation, compliance, and patient safety
Apply now to begin your career in Pharmacovigilance and Drug Safety with Accenture through thepharmadaily.com.
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