Accenture has announced new openings for Pharmacovigilance and Regulatory Affairs jobs in India, offering opportunities for both freshers and experienced life-science and pharmacy professionals. Three positions are currently listed across Chennai and Bengaluru, including Pharmacovigilance Services New Associate, Pharmacovigilance Services Associate, and LifeScience Regulatory Svs Associate.
The Accenture Pharmacovigilance jobs involve drug safety surveillance, Individual Case Safety Report (ICSR) processing, MedDRA coding, safety database activities, follow-up and regulatory compliance. The Regulatory Affairs opening focuses on global regulatory submissions, eCTD publishing, document QC, lifecycle management and regulatory operations.
Candidates with BSc, BDS, B.Pharm or M.Pharm qualifications, depending on the position, can review the eligibility criteria below and apply through the official Accenture careers portal.
Accenture Job Openings 2026
| Role | Location | Qualification | Experience |
|---|---|---|---|
| Pharmacovigilance Services New Associate | Chennai | BSc / BDS / B.Pharm | 0โ1 Year |
| Pharmacovigilance Services Associate | Chennai | B.Pharm / M.Pharm | 1โ3 Years |
| LifeScience Regulatory Svs Associate | Bengaluru | M.Pharm | 1โ3 Years |
1. Pharmacovigilance Services New Associate
Location: Chennai
Experience: 0โ1 Year
Qualification: BSc / Bachelor of Dental Surgery (BDS) / Bachelor of Pharmacy (B.Pharm)
Job ID: AIOC-S01663135
This entry-level Accenture Pharmacovigilance job in Chennai is suitable for candidates looking to start or build a career in drug safety and pharmacovigilance.
Key Responsibilities
- Perform product safety monitoring and drug safety surveillance.
- Support identification and creation of safety cases.
- Enter adverse event and safety information into the safety database.
- Perform appropriate MedDRA coding.
- Support Individual Case Safety Report (ICSR) processing.
- Handle case submissions according to client procedures and regulatory requirements.
- Perform follow-up activities for safety cases.
- Follow established SOPs, guidelines and quality requirements.
- Work as an individual contributor within a pharmacovigilance team.
- Be prepared to work rotational shifts where required.
Who Can Apply?
Candidates with BSc, BDS or B.Pharm and 0โ1 year of experience can apply. This makes the opening particularly relevant for freshers and early-career candidates seeking pharmacovigilance opportunities.
2. Pharmacovigilance Services Associate
Location: Chennai
Experience: 1โ3 Years
Qualification: B.Pharm / M.Pharm
Job ID: AIOC-S01663136
The Pharmacovigilance Services Associate position focuses primarily on ICSR processing and operational pharmacovigilance activities.
Key Responsibilities
- Perform intake, review, assessment and processing of adverse event reports.
- Handle Individual Case Safety Report processing.
- Perform case identification and safety database entry.
- Conduct MedDRA coding.
- Manage pharmacovigilance case processing activities.
- Support regulatory submission of safety cases.
- Perform written follow-ups for serious and non-serious cases.
- Support affiliate mailbox management.
- Perform reconciliation of safety reports according to defined processes.
- Maintain compliance with global pharmacovigilance regulations and client quality standards.
Who Can Apply?
Candidates with a B.Pharm or M.Pharm qualification and 1โ3 years of relevant experience can apply.
3. LifeScience Regulatory Svs Associate
Location: Bengaluru โ BDC9A
Experience: 1โ3 Years
Qualification: M.Pharm
Job ID: AIOC-S01663138
Accenture is also hiring for a Life Sciences Regulatory Affairs Associate in Bengaluru. This position focuses on regulatory operations, submission publishing, document quality control and lifecycle management.
Key Responsibilities
- Support end-to-end planning and coordination of global regulatory submissions.
- Compile, publish and dispatch regulatory lifecycle submissions.
- Perform bookmarking and hyperlinking of submission documents.
- Review and transform source documents.
- Perform document and submission-component QC.
- Ensure dossiers comply with regional regulatory requirements.
- Work with eCTD standards and applicable health authority guidelines.
- Support renewals, variations, supplements and annual reports.
- Manage post-approval regulatory lifecycle activities.
- Track submission readiness and identify documentation gaps.
- Collaborate with cross-functional stakeholders.
- Support health authority interactions and responses.
- Work with Regulatory Information Management Systems (RIMS) and regulatory publishing tools.
- Support compliant and timely submission execution.
Who Can Apply?
Candidates with a Master of Pharmacy (M.Pharm) and 1โ3 years of relevant experience can apply for this Accenture Regulatory Affairs opening.
Apply: Accenture LifeScience Regulatory Svs Associate
Skills Relevant to These Accenture Jobs
Candidates applying for these openings may benefit from knowledge or experience in:
Pharmacovigilance: ICSR processing, adverse event reporting, drug safety surveillance, MedDRA coding, case follow-up, safety databases, case reconciliation and global PV regulations.
Regulatory Affairs: eCTD, regulatory publishing, document QC, submission lifecycle management, RIMS, health authority requirements, regulatory operations and submission compilation.
Why Consider These Opportunities?
These roles provide exposure to global life-sciences operations within Accenture. Depending on the position, candidates can develop practical expertise in pharmacovigilance case processing, drug safety, regulatory operations, eCTD publishing and global regulatory submissions.
The Pharmacovigilance Services New Associate opening is especially notable because Accenture specifies 0โ1 year of experience, creating an opportunity for eligible early-career candidates.
How to Apply
Application Link For Pharmacovigilance Services New Associate
Application Link For Pharmacovigilance Services Associate
Application Link For LifeScience Regulatory Svs Associate
