Accenture has opened applications for multiple roles under its Life Sciences R&D division in India. The company is currently hiring for Pharmacovigilance, Drug Safety, Regulatory Affairs, Clinical Data Management, and Medical Affairs positions in Bengaluru and Chennai.
These openings are suitable for candidates with qualifications such as B.Pharm, M.Pharm, MBBS, BE, and MCA along with relevant industry experience.
Candidates looking for pharmacovigilance jobs in India, drug safety associate jobs, regulatory affairs openings, and clinical data management careers can explore these opportunities at Accenture.
1. Pharmacovigilance Services Associate โ Bengaluru
| Details | Information |
|---|---|
| Role | Pharmacovigilance Services Associate |
| Location | Bengaluru |
| Qualification | B.Pharm / M.Pharm |
| Experience | 1โ3 Years |
| Job ID | AIOC-S01647839 |
Job Description
The selected candidates will work in Pharmacovigilance Operations and Drug Safety Surveillance activities. The role involves monitoring the safety of pharmaceutical products and processing Individual Case Safety Reports (ICSRs).
Key Responsibilities
- Case identification and intake
- Adverse event data entry
- MedDRA coding
- ICSR processing
- Regulatory submission support
- Safety database management
- Follow-up activities for safety cases
- Compliance with global pharmacovigilance regulations
Required Skills
- Pharmacovigilance operations
- Drug safety surveillance
- MedDRA coding
- ICSR lifecycle management
- Attention to detail
- Team collaboration
Salary Range
โน4.5 โ โน7.5 LPA
2. Pharmacovigilance Services Analyst โ Bengaluru
| Details | Information |
|---|---|
| Role | Pharmacovigilance Services Analyst |
| Location | Bengaluru |
| Qualification | B.Pharm / M.Pharm |
| Experience | 3โ5 Years |
| Job ID | AIOC-S01647840 |
Job Description
This role is designed for experienced pharmacovigilance professionals with expertise in drug safety operations and case processing.
Key Responsibilities
- Advanced ICSR processing
- Medical review coordination
- Safety data analysis
- MedDRA coding and validation
- Regulatory compliance activities
- Handling safety follow-ups
- Maintaining quality standards in PV operations
Required Skills
- Senior drug safety experience
- Pharmacovigilance database knowledge
- Signal management understanding
- Regulatory compliance
- Case quality review
Salary Range
โน7 โ โน11 LPA
3. Pharmacovigilance Services Specialist โ Chennai
| Details | Information |
|---|---|
| Role | Pharmacovigilance Services Specialist |
| Location | Chennai |
| Qualification | MBBS |
| Experience | 0โ4 Years |
| Job ID | AIOC-S01647552 |
Job Description
The role falls under Medical Affairs and Pharmacovigilance Services. Candidates will support pharmaceutical medical affairs operations and scientific communication initiatives.
Key Responsibilities
- Medical affairs support
- Scientific documentation
- Medical publications
- Advisory board coordination
- Medical information handling
- Drug safety evaluation
- Advocacy and educational activities
Required Skills
- Clinical knowledge
- Medical communication
- Analytical skills
- Adaptability
- Team collaboration
Salary Range
โน8 โ โน14 LPA
4. Clinical Data Services Associate โ Bengaluru
| Details | Information |
|---|---|
| Role | Clinical Data Services Associate |
| Location | Bengaluru |
| Qualification | BE / MCA |
| Experience | 1โ3 Years |
| Job ID | AIOC-S01563976 |
Job Description
The Clinical Data Management team supports clinical trial reporting, database programming, and validation activities for pharmaceutical studies.
Key Responsibilities
- Clinical report development
- SQL and PLSQL programming
- SAS Clinical reporting
- Database validation
- Query management
- UAT testing
- Clinical data review
- CRF and eCRF management
Required Skills
- SAS Clinical
- SQL / PLSQL
- Clinical Data Management
- Database programming
- Problem-solving skills
Salary Range
โน5 โ โน9 LPA
5. LifeScience Regulatory Services Analyst โ Bengaluru
| Details | Information |
|---|---|
| Role | LifeScience Regulatory Services Analyst |
| Location | Bengaluru |
| Qualification | B.Pharm |
| Experience | 3โ5 Years |
| Job ID | AIOC-S01647847 |
Job Description
The Regulatory Services team supports pharmaceutical regulatory submissions and lifecycle management activities across global markets.
Key Responsibilities
- Regulatory documentation management
- Global application filing support
- eCTD submission handling
- Lifecycle management submissions
- Annual reports and amendments
- SPL submissions
- Compliance tracking
Required Skills
- Regulatory affairs operations
- eCTD submissions
- Documentation management
- Stakeholder coordination
- Deadline management
Salary Range
โน6 โ โน10 LPA
Why Join Accenture Life Sciences Division?
Working with Accenture Careers offers strong career growth opportunities in pharmacovigilance, regulatory affairs, and clinical research domains.
Employee Benefits
- Global pharmaceutical project exposure
- Learning and development programs
- Career growth opportunities
- International work culture
- Hybrid and operational flexibility
- Exposure to top pharma clients
- Competitive salary packages
How to Apply
Application Link For Pharmacovigilance Services Associate
Application Link For Pharmacovigilance Services Associate
Application Link For Pharmacovigilance Services Specialist
Application Link For Pharmacovigilance Services Analyst
Application Link For Clinical Data Svs Associate
Application Link For LifeScience Regulatory Svs Analyst