Pharmacovigilance Services Associate
Location: Mumbai, India
Job Type: Full-Time
Experience Required: 0–2 years
Job ID: AIOC-S01614128
Category: Pharmacovigilance | Drug Safety | Clinical Research
About the Role
Accenture is seeking a Pharmacovigilance Services Associate to join our Life Sciences R&D vertical. In this role, you will support global pharmacovigilance operations, ensuring the accurate processing, coding, and reporting of adverse events in compliance with client-specific guidelines and global regulatory requirements. This position provides hands-on exposure to the full scope of pharmacovigilance, including case identification, data entry, MedDRA coding, ICSR processing, and follow-up for both serious and non-serious cases.
This is an excellent opportunity for early-career professionals in pharmacy or life sciences to develop expertise in drug safety, regulatory compliance, and pharmacovigilance systems within a global, collaborative environment.
Key Responsibilities
Manage and monitor affiliate mailboxes for incoming safety reports and queries.
Process Individual Case Safety Reports (ICSRs) in compliance with client SOPs and global regulatory standards.
Perform data entry, MedDRA coding, case processing, submission, and follow-ups for serious and non-serious adverse events.
Reconcile safety reports according to defined processes and timelines.
Assist in maintaining accurate and up-to-date safety databases.
Collaborate with cross-functional teams to ensure timely resolution of queries and data discrepancies.
Apply established procedures and guidelines to routine case management, escalating complex issues to supervisors.
May work in rotational shifts as per operational requirements.
Education & Experience Requirements
Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).
0–2 years of relevant experience in pharmacovigilance, drug safety, or clinical research operations.
Exposure to pharmacovigilance operations, safety databases, or ICSR processing is preferred.
Required Skills & Competencies
Knowledge of pharmacovigilance processes, adverse event reporting, and safety data management.
Familiarity with global regulatory requirements for pharmacovigilance (FDA, EMA, ICH).
Strong attention to detail, analytical skills, and ability to follow SOPs accurately.
Good written and verbal communication skills in English.
Ability to work effectively as an individual contributor within a team environment.
Basic computer skills, including MS Office and database operations.
Adaptability to work in rotational shifts if required.
About Accenture
Accenture is a leading global professional services company with capabilities in digital, cloud, security, and life sciences. We combine deep industry expertise with advanced technology and innovation to deliver meaningful solutions for our clients worldwide.
With over 699,000 employees serving clients in more than 120 countries, we foster an inclusive, diverse, and collaborative workplace where employees are empowered to learn, grow, and succeed.
Learn more at: www.accenture.com
Equal Opportunity & Compliance
Accenture is an Equal Employment Opportunity Employer. Employment decisions are made without regard to age, race, color, religion, sex, national origin, disability, veteran status, sexual orientation, gender identity, marital status, or any other legally protected status.
Important Notice: Accenture does not charge candidates for employment. Fraudulent messages requesting payment should be reported immediately to india.fc.check@accenture.com.
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