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Pharmacovigilance Services New Associate
Accenture
Bengaluru
0–1 Years
Pharmacovigilance
Drug Safety
Life Sciences
🏢 About Accenture
Accenture is a global professional services company providing digital transformation, technology, consulting, and life sciences services. With more than 790,000 employees across 120+ countries, Accenture supports global pharmaceutical companies in clinical research, pharmacovigilance operations, and regulatory compliance.
📌 Job Overview
- Role: Pharmacovigilance Services New Associate
- Company: Accenture
- Location: Bengaluru, India
- Experience: 0–1 Years
- Qualification: MSc (Life Sciences) / M.Pharm
- Department: Pharmacovigilance Operations
- Employment Type: Full-Time
🔬 Key Responsibilities
- Identify and process Individual Case Safety Reports (ICSRs)
- Perform safety data entry in pharmacovigilance databases
- MedDRA coding for adverse event reporting
- Support adverse event follow-ups and case management
- Assist with drug safety surveillance activities
- Maintain compliance with global pharmacovigilance regulations
- Collaborate with drug safety teams and supervisors
- Support post-marketing safety data monitoring
🎓 Eligibility Criteria
- MSc (Life Sciences)
- Master of Pharmacy (M.Pharm)
- 0–1 year experience in pharmacovigilance or drug safety
- Knowledge of adverse event reporting and safety data processing
- Understanding of ICSR workflows and MedDRA terminology
- Good communication and analytical skills
- Willingness to work in rotational shifts
⭐ Why Join Accenture?
- Exposure to global pharmacovigilance projects
- Work with leading pharmaceutical companies
- Training in drug safety systems and regulatory compliance
- Strong career growth in pharmacovigilance and regulatory operations
- Global work environment with advanced technologies
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Candidates with knowledge of pharmacovigilance workflows, adverse event reporting, and MedDRA coding may have an advantage during the selection process.
Kindly read the entire job description carefully before applying. Candidates with knowledge of pharmacovigilance workflows, adverse event reporting, and MedDRA coding may have an advantage during the selection process.
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