Pharmacovigilance Services New Associate Drug Safety Jobs at Accenture
Company Overview
Accenture is a globally recognized professional services organization known for delivering innovative solutions across technology, operations, consulting, and digital transformation. With a workforce of hundreds of thousands of professionals operating in more than 120 countries, Accenture supports leading pharmaceutical, life sciences, healthcare, and biotechnology companies worldwide. Pharmacovigilance Services New Associate
In the life sciences domain, Accenture provides end-to-end pharmacovigilance, drug safety, regulatory, and clinical operations services. The organization operates large global delivery centers that support regulated markets by ensuring compliance, patient safety, and data integrity. Accenture offers a structured work environment, strong learning culture, and long-term career development opportunities for early-career professionals entering the pharmacovigilance field. Pharmacovigilance Services New Associate
Job Location & Employment Type
- Job Location: Bengaluru, Karnataka
- Employment Type: Full-time, permanent
- Industry: Pharmacovigilance / Drug Safety
- Job Level: Entry-level / Associate
- Work Model: Office-based (as per project requirement)
Open Positions / Department Details
Accenture is currently hiring for the following role within its pharmacovigilance operations team:
Position Title: Pharmacovigilance Services – New Associate
Department: Pharmacovigilance & Drug Safety Surveillance
Job Requisition ID: AIOC-S01621687
This role is ideal for freshers and early-career professionals who want to build a long-term career in drug safety and global pharmacovigilance operations. Pharmacovigilance Services New Associate
Key Roles & Responsibilities
As a Pharmacovigilance Services New Associate, the selected candidate will support end-to-end safety case processing activities in compliance with global regulatory standards. Key responsibilities include: Pharmacovigilance Services New Associate
- Identifying, reviewing, and creating Individual Case Safety Reports (ICSRs) in the global safety database
- Processing safety cases received through intake workflows, client mailboxes, electronic gateways, and other approved sources
- Performing triage, prioritization, and case booking activities as per regulatory timelines and client SOPs
- Conducting accurate data entry, medical coding, and narrative writing for adverse event cases
- Evaluating serious and non-serious adverse events in compliance with regulatory requirements
- Handling follow-up requests, retrieving missing safety information, and resolving data discrepancies
- Performing duplicate checks and ensuring case validity before processing
- Coding adverse events and suspect drugs using MedDRA and WHO-Drug dictionaries
- Assessing seriousness, causality, and expectedness of adverse events in coordination with medical reviewers
- Submitting AE, SAE, and SUSAR cases within defined timelines using the global safety database
- Supporting submission troubleshooting and monitoring regulatory report transmission
- Maintaining Trial Master File (TMF) and archiving safety documentation accurately
- Monitoring and reconciling safety mailboxes and intake sources
- Supporting unblinding activities (paper or electronic) as per SOPs, when applicable
- Assisting in audits, inspections, reconciliation activities, and transition-related tasks
- Performing case corrections, deletions, and quality reviews within approved timelines
- Supporting pharmacovigilance meetings, documentation, and internal quality checks
Pharmacovigilance Services New Associate
Eligibility Criteria
Education
Candidates must possess one of the following qualifications:
- Bachelor of Ayurvedic Medicine and Surgery (BAMS)
- B.Sc Nursing
- Bachelor’s Degree in Life Sciences or related discipline
Experience
- Experience Range: 0 to 1 year
- Freshers with relevant academic background are eligible
- Prior exposure to pharmacovigilance or drug safety is an added advantage but not mandatory
Skills Required
- Basic understanding of pharmacovigilance and drug safety concepts
- Knowledge of medical terminology and safety case processing workflows
- Familiarity with MedDRA and WHO-Drug dictionaries (preferred)
- Proficiency in MS Office applications
- Strong written and verbal communication skills
- High level of English language proficiency (reading, writing, speaking, listening)
- Good medical writing and documentation skills
- Attention to detail and ability to work with quality metrics
- Willingness to learn and adapt to different pharmacovigilance roles
Salary & Benefits
- Salary: As per company norms
Additional benefits may include:
- Comprehensive training in pharmacovigilance and drug safety operations
- Exposure to global safety databases and regulatory standards
- Opportunity to work with international pharmaceutical clients
- Structured learning paths and internal certification programs
- Stable employment with a globally reputed organization
- Inclusive and diversity-driven workplace culture
Final compensation details will be discussed during the hiring process.
Selection Process
The recruitment process generally includes:
- Application screening
- Assessment or technical evaluation (if applicable)
- Interview rounds (technical and HR)
- Final selection based on eligibility and performance
Candidates must successfully complete all mandatory training programs post-selection. Pharmacovigilance Services New Associate
How to Apply
Interested and eligible candidates can apply through Accenture’s official career portal.
Job Title: Pharmacovigilance Services New Associate
Job Location: Bengaluru
Requisition ID: AIOC-S01621687
Candidates are advised to ensure accuracy of details while applying and keep relevant educational documents ready for verification. Pharmacovigilance Services New Associate
Important Dates
- Job Posted: 23 days ago
- Application Mode: Online application
- Last Date: Not specified (apply at the earliest)
Why Apply for This Pharma Job?
This role is an excellent starting point for graduates looking to enter the pharmacovigilance and drug safety domain. Accenture offers structured onboarding, strong compliance training, and exposure to global safety reporting standards, making it an ideal platform for building a long-term career in pharmacovigilance. Pharmacovigilance Services New Associate
Working with Accenture allows professionals to gain experience in global safety databases, regulatory submissions, and cross-functional collaboration. The organization’s scale, learning culture, and internal mobility provide strong career progression opportunities for motivated candidates. Pharmacovigilance Services New Associate
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with Accenture or its recruitment team. All job details are shared for informational purposes only. Candidates are advised to verify job authenticity and application details through official company sources before applying.
Accenture follows an equal employment opportunity policy and does not charge any fees for recruitment. Pharmacovigilance Services New Associate
Final Call-to-Action
If you are a life sciences graduate or healthcare professional looking to start your career in pharmacovigilance and drug safety, this opportunity with Accenture offers structured training, global exposure, and long-term career stability. Apply promptly and take your first step into the world of regulated drug safety operations. Pharmacovigilance Services New Associate
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