Latest pharma jobs Pharmacovigilance Services Analyst Accenture job for freshers and experienced candidates apply online with eligibility and salary details
Introduction
Looking to build a stable career in drug safety and pharmacovigilance? The Pharmacovigilance Services Analyst Accenture Job 2026 is an excellent opportunity for life sciences and pharmacy graduates to work with a globally recognized organization. This role focuses on safety writing, adverse event analysis, and regulatory compliance, making it ideal for professionals aiming to grow in pharmacovigilance operations.
Job Overview
| Details | Information |
|---|---|
| Job Title | Pharmacovigilance Services Analyst |
| Company Name | Accenture |
| Location | Chennai, India |
| Employment Type | Full-Time |
| Department | Pharmacovigilance / Life Sciences R&D |
| Experience Required | 3–5 Years |
| Education | Any Graduation (Life Sciences/Pharmacy Preferred) |
| Salary | As per company norms |
Company Overview
Accenture is one of the world’s leading professional services firms, offering expertise in digital transformation, cloud solutions, and intelligent operations. With operations in more than 120 countries, the company supports industries including healthcare and life sciences by delivering advanced solutions across clinical research, pharmacovigilance, and regulatory domains.
Its Life Sciences division works closely with global biopharma companies to improve patient outcomes by integrating scientific knowledge with real-world insights.
Job Location & Employment Type
This opportunity is based in Chennai, India, and is a full-time role. Candidates should be open to working in rotational shifts, depending on project requirements.
Open Positions / Department Details
The position is part of the Pharmacovigilance Operations team within the Life Sciences R&D vertical. This team plays a critical role in ensuring drug safety by monitoring adverse events and maintaining compliance with regulatory standards.
Key functional area includes:
- Pharmacovigilance operations
- Safety writing and reporting
- Regulatory documentation
- Clinical data interpretation
Key Roles & Responsibilities
As a Pharmacovigilance Services Analyst, your core responsibilities will include:
- Preparing and reviewing individual case safety narratives for regulatory submissions
- Analyzing adverse event data from clinical trials and post-marketing sources
- Developing high-quality scientific and medical content for safety documentation
- Supporting medical, legal, and regulatory (MLR) review processes
- Responding to review queries and implementing necessary updates
- Writing scientific documents such as manuscripts, white papers, and reports
- Ensuring compliance with regulatory guidelines and SOPs
- Converting clinical data into structured regulatory formats
- Collaborating with cross-functional teams including technology and creative departments
- Maintaining high-quality standards in all deliverables
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in:
- Pharmacy
- Life Sciences
- Medical or related discipline
Experience
- 3 to 5 years of relevant experience in:
- Pharmacovigilance
- Medical writing
- Safety data review
Skills Required
- Strong understanding of pharmacovigilance processes
- Experience in medical referencing and documentation
- Knowledge of global regulatory requirements
- Familiarity with tools like Veeva Vault (preferred)
- Proficiency in MS Office (Excel, Word, PowerPoint, Outlook)
- Excellent communication and teamwork abilities
- Strong attention to detail and analytical thinking
Salary & Benefits
Salary: As per company norms
Benefits include:
- Health and wellness support
- Career development opportunities
- Exposure to global pharmaceutical projects
- Learning and certification programs
- Inclusive and diverse work environment
Selection Process
The recruitment process for the Pharmacovigilance Services Analyst Accenture Job typically includes:
- Application screening
- Assessment or technical evaluation
- Interview (technical + HR rounds)
- Final selection and offer rollout
How to Apply
Candidates can apply through the online application process:
- Visit the official careers portal of Accenture
- Search using Job ID: AIOC-S01641318
- Fill in the application form
- Upload your updated resume
- Submit the application
Apply early to increase your chances of selection.
Important Dates
- Last date to apply: Not specified
Why Apply for This Job?
The Pharmacovigilance Services Analyst Accenture Job 2026 offers strong career advantages:
- Opportunity to work with a global leader in healthcare and technology
- Hands-on experience in pharmacovigilance and drug safety
- Exposure to international regulatory standards
- Growth in medical writing and safety reporting
- Stable and structured career path in life sciences
- Opportunity to work on high-impact global projects
This role is ideal for professionals aiming to grow in drug safety, regulatory affairs, or clinical research domains.
FAQs
1. What is the focus keyword for this job?
The focus keyword is Pharmacovigilance Services Analyst Accenture Job.
2. What experience is required for this role?
Candidates need 3 to 5 years of experience in pharmacovigilance or related fields.
3. Is this role suitable for freshers?
No, this position requires prior experience in drug safety or medical writing.
4. What is the job location?
The job is based in Chennai, India.
5. What skills are essential for this role?
Knowledge of pharmacovigilance, medical writing, regulatory compliance, and MS Office tools is essential.
Conclusion
The Pharmacovigilance Services Analyst Accenture Job 2026 is a valuable opportunity for experienced professionals in drug safety and medical writing. With strong global exposure, career growth potential, and involvement in critical healthcare projects, this role can significantly enhance your career in pharmacovigilance. Interested candidates should apply online at the earliest.
Disclaimer
LatestPharmaJobs.in is an independent job information platform. We do not provide jobs or recruitment and are not affiliated with any company.