Job Title:
Pharmacovigilance Services Associate
Employer:
Accenture
Location:
Bengaluru, India
Job Type:
Full-Time
Experience Required:
0 – 2 years (Freshers eligible)
Job Reference No.:
AIOC-S01605314
About Accenture:
Accenture is a global professional services company with leading expertise in digital, cloud, and security.
With operations in 120+ countries and a workforce of 775,000+ professionals, Accenture helps clients across 40+ industries by combining innovation and technology to deliver human-centered solutions.
The company offers services in:
Strategy & Consulting
Technology & Operations
Accenture Song
🌐 Website: www.accenture.com
Department:
Life Sciences R&D – Clinical, Pharmacovigilance & Regulatory
Overview:
This role falls under the Life Sciences R&D vertical, which supports the pharmaceutical and biotechnology industry across research, clinical, regulatory, and safety functions.
You will contribute to pharmacovigilance and drug safety surveillance — ensuring the collection, processing, and reporting of adverse events comply with global standards and regulations.
Job Description:
As a Pharmacovigilance Services Associate, you will assist in monitoring drug safety activities, case management, and regulatory submissions.
You will work as part of a team responsible for managing Individual Case Safety Reports (ICSRs) and ensuring timely and accurate reporting.
Key Responsibilities:
Manage Affiliate Mailbox and perform report reconciliation as per process guidelines.
Conduct written follow-up activities for both serious and non-serious cases.
Handle case identification, data entry, MedDRA coding, case processing, submission, and follow-up in safety databases.
Ensure compliance with client guidelines and global regulatory requirements (e.g., ICH, EMA, FDA).
Solve routine pharmacovigilance issues using standard guidelines and past precedents.
Communicate effectively within the team and report to supervisors.
Follow detailed instructions for new tasks and moderate guidance for daily operations.
Perform as an individual contributor in a focused workstream.
Be flexible to work in rotational shifts as per project needs.
Qualifications:
🎓 Required Education:
Bachelor of Pharmacy (B.Pharm)
Master of Pharmacy (M.Pharm)
💼 Preferred Experience:
1–3 years in pharmacovigilance, drug safety, or related areas (Freshers may apply)
Skills Required:
Knowledge of pharmacovigilance operations and drug safety processes
Familiarity with ICSR workflow and safety databases
Understanding of MedDRA coding and regulatory reporting timelines
Strong analytical and documentation skills
High attention to detail and accuracy
Good communication and team collaboration skills
Ability to work under minimal supervision and meet strict timelines
Equal Employment Opportunity Statement:
Accenture provides equal employment opportunities regardless of age, race, creed, color, religion, sex, national origin, disability, sexual orientation, gender identity, or any other status protected by law.
Recruitment Fraud Alert:
Accenture does not charge any fees during the recruitment process.
If you receive a message asking for payment or personal banking information, report it immediately to:
📧 india.fc.check@accenture.com
Why Join Accenture?
✅ Work with leading global clients in life sciences and healthcare.
✅ Be part of a diverse, innovative, and inclusive work culture.
✅ Receive continuous learning and certification opportunities.
✅ Access holistic well-being programs (physical, mental, financial).
✅ Work in a recognized World’s Best Workplace™.
🌍 Join Accenture — Work at the Heart of Change.
🔗 www.accenture.com
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