Global professional services leader Accenture is actively hiring for multiple Life Sciences and Healthcare roles in Bengaluru. The company is recruiting Pharmacovigilance Services Associates and Clinical Data Services Associates for its Clinical, Pharmacovigilance, and Regulatory Operations teams.
Candidates with B.Pharm, M.Pharm, and relevant healthcare or life sciences backgrounds looking for pharmacovigilance jobs in Bengaluru, drug safety jobs, ICSR processing jobs, and clinical data management careers should explore these opportunities.
About Accenture
Accenture is a global professional services company specializing in digital transformation, cloud computing, artificial intelligence, consulting, and operations. With more than 791,000 employees serving clients across 120+ countries, Accenture supports leading pharmaceutical, biotechnology, and healthcare organizations worldwide.
The company’s Life Sciences R&D division helps biopharmaceutical companies accelerate research, regulatory compliance, pharmacovigilance operations, and clinical development programs.
1. Pharmacovigilance Services Associate
Job Location: Bengaluru, Karnataka, India
Job Type: Full-Time
Experience Required: 1โ3 Years
Qualification: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm)
Key Responsibilities
- Perform Individual Case Safety Report (ICSR) processing.
- Conduct case identification and case intake activities.
- Review adverse event reports and source documents.
- Perform MedDRA coding and safety database entry.
- Assess case validity and perform duplicate checks.
- Evaluate seriousness, causality, and expectedness of adverse events.
- Prepare and update case narratives.
- Conduct follow-up activities for missing safety information.
- Support medical reviewers with safety issue identification.
- Complete quality checks and compliance reviews.
- Ensure adherence to regulatory timelines, SLA requirements, and client guidelines.
Required Skills
- Pharmacovigilance and Drug Safety Surveillance
- ICSR Processing
- MedDRA Coding
- Case Narrative Writing
- Adverse Event Assessment
- Safety Database Management
- Regulatory Compliance
- Attention to Detail
2. Clinical Data Services Associate
Job Location: Bengaluru, Karnataka, India
Job Type: Full-Time
Experience Required: 1โ3 Years
Qualification: BE, B.Pharm, or M.Pharm
Key Responsibilities
- Support clinical data management and medical monitoring activities.
- Review and validate protocol requirement specifications.
- Assist with clinical trial data processing and quality review.
- Ensure compliance with clinical research and regulatory standards.
- Monitor data consistency and support trial oversight activities.
- Collaborate with clinical operations teams to maintain data quality.
Required Skills
- Clinical Data Management
- Medical Monitoring
- Clinical Research Operations
- Protocol Review
- Data Validation
- Communication Skills
- Problem Solving
- Adaptability
Eligibility Criteria
Candidates should possess:
- B.Pharm or M.Pharm degree for Pharmacovigilance Associate roles.
- BE, B.Pharm, or M.Pharm degree for Clinical Data Services Associate roles.
- 1โ3 years of relevant industry experience.
- Strong written and verbal communication skills.
- Ability to work in rotational shifts.
- Knowledge of pharmacovigilance regulations, ICSR processing, or clinical data management.
Why Join Accenture?
- Work with leading global pharmaceutical companies.
- Exposure to advanced pharmacovigilance and clinical research projects.
- Career growth within Life Sciences and Healthcare Operations.
- Opportunity to develop expertise in drug safety and clinical data management.
- Inclusive and diverse work environment.
- Competitive compensation and employee benefits.
How to Apply
Application Link For Clinical Data Services Associate
Application Link For Pharmacovigilance Services Associate
Application Link For Pharmacovigilance Services Associate
