Accenture is hiring for the position of Pharmacovigilance Services Associate in Bengaluru, Karnataka. The role focuses on pharmacovigilance operations, drug safety surveillance, Individual Case Safety Report (ICSR) processing, medical coding, regulatory submissions, and case follow-ups.
Candidates with a Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) qualification can apply for this opportunity.
Job Details
| Particulars | Details |
|---|---|
| Company | Accenture |
| Job Title | Pharmacovigilance Services Associate |
| Designation | Drug Safety Associate |
| Job Location | Bengaluru, Karnataka |
| Employment Type | Full Time |
| Experience | 0–2 years (job overview); 1–3 years (job description) |
| Required Qualification | B.Pharm / M.Pharm |
| Primary Skill | Pharmacovigilance & Drug Safety Surveillance |
| Job Number | AIOC-S01665479 |
| Shift | Rotational shifts may be required |
Position: Pharmacovigilance Services Associate
The selected candidate will support drug safety operations by processing safety reports, managing case data, performing MedDRA coding, handling follow-ups, and ensuring compliance with client guidelines and applicable global regulatory requirements.
Roles and Responsibilities
- Manage affiliate mailbox reconciliation and reports according to established processes.
- Perform written follow-up attempts for both serious and non-serious cases.
- Identify and manage Individual Case Safety Reports (ICSRs).
- Perform safety case data entry and MedDRA coding.
- Process and submit safety cases in the safety database.
- Conduct case follow-ups according to client guidelines and applicable global regulatory requirements.
- Resolve routine problems using established procedures and general guidelines.
- Work as an individual contributor within a team under the guidance of a direct supervisor.
Eligibility and Qualifications
Candidates must have one of the following qualifications:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
The job overview lists 0–2 years of experience, while the detailed job description lists 1–3 years.
Required Skills
- Pharmacovigilance operations
- Drug safety surveillance
- ICSR identification and processing
- MedDRA coding
- Safety database data entry
- Regulatory case submissions and follow-ups
- Written communication for case follow-ups
- Ability to follow client guidelines and established procedures
