Accenture Hiring Pharmacovigilance Services Analyst

Pharmacovigilance Analyst – Life Sciences – Chennai 

Accenture hiring Pharmacovigilance Services Analyst in Chennai. Life Sciences graduates with 3–5 years experience eligible. Full-time role.

Accenture has opened a full-time opportunity for the role of Pharmacovigilance Services Analyst in Chennai. This position is designed for experienced life sciences professionals who want to work in global drug safety operations, regulatory compliance, and pharmacovigilance quality management. The role sits at the intersection of patient safety, regulatory science, and operational excellence, offering strong career growth within one of the world’s most respected professional services organizations. Candidates with hands-on experience in pharmacovigilance operations, drug safety surveillance, and quality management systems will find this role both challenging and rewarding.

Company Overview

Accenture is a global professional services company known for its leadership in digital transformation, cloud computing, security, and intelligent operations. With operations in over 120 countries and a workforce of nearly 700,000 professionals, Accenture supports global pharmaceutical, biotechnology, and healthcare organizations across the full product lifecycle.

In pharmacovigilance and drug safety, Accenture partners with leading life sciences companies to deliver high-quality case processing, regulatory compliance, audit readiness, and safety surveillance services. Working at Accenture provides exposure to global regulatory frameworks, advanced pharmacovigilance systems, and enterprise-level quality management practices, making it a strong credential for long-term careers in drug safety and regulatory affairs.

Job Role & Responsibilities

The Pharmacovigilance Services Analyst plays a critical role in maintaining quality, compliance, and operational efficiency within pharmacovigilance engagements. The role focuses heavily on quality management frameworks, regulatory adherence, and continuous process improvement.

Key Responsibilities

• Ensure adherence to Pharmacovigilance Quality Management Framework procedures
• Review project Quality Management Systems and recommend process improvements
• Collaborate with Team Leads, Trainers, and Medical Reviewers to enhance existing processes
• Coordinate with Quality Reviewers to ensure compliance with SOPs and client requirements
• Review late case logs and manage Root Cause Analysis (RCA) and Corrective and Preventive Actions (CAPA)
• Follow up with cross-functional stakeholders to ensure timely documentation and submission
• Support training programs, refresher sessions, and awareness workshops for PV teams
• Work with Capability Development and Operational Excellence teams to improve engagement quality
• Identify quality gaps, learning opportunities, and compliance risks
• Collaborate with client quality and training teams to share best practices
• Draft meeting agendas, minutes, and maintain accurate documentation archives
• Review safety case data for completeness, accuracy, and regulatory compliance
• Track, submit, and distribute pharmacovigilance and quality reports
• Support audits, inspections, and regulatory authority interactions
• Drive zero quality deviations leading to late regulatory submissions
• Ensure monthly compliance with Service Level Agreements (SLAs)
• Support SOP development, review, and maintenance
• Monitor and reconcile client mailboxes, SharePoint, and safety databases
• Assist in transition activities and system access requests
• Troubleshoot discrepancies in client tools and pharmacovigilance databases

This role targets high CPC domains such as pharmacovigilance analyst jobs, drug safety compliance roles, regulatory affairs services, life sciences consulting, and healthcare quality management.

Eligibility / Qualifications

Educational Background

Candidates must hold one of the following qualifications:
Bachelor of Ayurvedic Medicine and Surgery (BAMS), Bachelor’s Degree in Life Sciences, Master’s Degree in Life Sciences

Experience Requirements

• 3 to 5 years of relevant experience in pharmacovigilance operations or drug safety surveillance
• Hands-on exposure to quality management systems within pharmacovigilance projects

Regulatory Knowledge & Skills

• Working knowledge of ICH, GCP, FDA, MHRA, and global pharmacovigilance regulations
• Strong understanding of medical terminology and safety case workflows
• High accuracy and attention to detail
• Strong written and verbal communication skills
• Effective interpersonal and stakeholder coordination skills
• Working knowledge of MS Excel, Word, and PowerPoint

Location & Employment Details

Job Location

• Chennai, Tamil Nadu

Employment Type

• Full-time, permanent role

Salary details are performance-based and aligned with industry standards for experienced pharmacovigilance professionals.

Application Process

Interested candidates must apply online through the official Accenture careers portal using the link below:

Apply here: https://www.accenture.com/in-en/careers/jobdetails?id=AIOC-S01621360_en&src=LINKEDINJP

Only shortlisted candidates will be contacted as per Accenture’s hiring process.

FAQs

Who is eligible for the Pharmacovigilance Services Analyst role at Accenture?

Candidates with BAMS, Life Sciences graduation, or postgraduation and 3–5 years of pharmacovigilance experience are eligible.

Is this a fresher-friendly role?

No. This role requires prior experience in pharmacovigilance and drug safety operations.

What regulatory exposure does this role offer?

The role involves working with global regulations including ICH, GCP, FDA, and MHRA guidelines.

Is this a permanent role?

Yes. This is a full-time position with Accenture.

Where is the job location?

The position is based in Chennai, Tamil Nadu.

Company	Accenture
Vacancies	Not Disclosed
Required Education	BAMS, Bachelor’s Degree in Life Sciences, Master’s Degree in Life Sciences
Experience	3–5 Years

Tagged as: Pharma Jobs in Bangalore, Pharma Jobs in Chennai