Pharmacovigilance Job at Accenture, Bengaluru
Looking for high-growth Pharmacovigilance and Drug Safety jobs in Bengaluru? Accenture is hiring Pharmacovigilance Services Associate Managers for its healthcare and life sciences operations. This Pharmacovigilance Job in Bengaluru is ideal for MBBS and MD professionals with expertise in aggregate reports, risk management plans, signal management, and safety writing. Candidates will work on global pharmacovigilance projects while collaborating with clients and regulatory stakeholders. If you are passionate about drug safety, medical review, and regulatory compliance, this opportunity at Accenture Careers could be an excellent opportunity to advance your career in pharmacovigilance.
About the Company:
Accenture is one of the world’s leading professional services organizations with expertise in digital, cloud, security, technology, consulting, and operations. With operations in more than 120 countries and a workforce of over 775,000 professionals, Accenture delivers innovative solutions across multiple industries including healthcare and life sciences. The company is known for its inclusive work culture, advanced technology ecosystem, and opportunities for continuous learning and professional growth.
Job Details:
- Job Role: Pharmacovigilance Services Associate Manager
- Job Location: Bengaluru, Karnataka, India
- Job Type: Full-time
- Experience Required: 3–14 years
- Functional Area: Pharmacovigilance Services – Safety Writing
- Job Number: AIOC-S01647306
- Industry: Healthcare / Life Sciences / Pharmacovigilance
Key Responsibilities:
- Perform medical review of aggregate reports and Risk Management Plans (RMP)
- Ensure compliance with client SOPs and global regulatory requirements in this Pharmacovigilance Job in Bengaluru
- Review aggregate data for medical relevance, consistency, and accuracy
- Participate in project planning and strategy meetings at Accenture Careers
- Address health authority comments and client medical queries
- Conduct signal management and safety profile assessments
- Review noteworthy clinical cases and published studies in this Job in Bengaluru
- Perform quality checks of aggregate reports and RMP documents
- Prepare medical analyses for safety-related sections of reports
- Provide conclusions regarding product safety profiles
- Support knowledge sharing, mentoring, and coaching activities
- Ensure adherence to SLAs, KPIs, and quality standards
- Manage adverse event narratives for regulatory submissions and safety reports
- Complete assigned pharmacovigilance and compliance trainings within timelines
Educational Requirements for this Pharmacovigilance Job:
- An MBBS qualification from a recognized institution
- MD qualification preferred
- Additional expertise in Pharmacovigilance or Drug Safety will be advantageous
Skills Required:
- Strong knowledge of Pharmacovigilance and Drug Safety practices
- Experience in Aggregate Reports (AR), Risk Management Plans (RMP), and Signal Management
- Safety writing and medical review expertise
- Understanding of global regulatory requirements and SOPs
- Strong analytical and medical interpretation skills
- Excellent written and verbal English communication
- Quality control and documentation skills
- Ability to mentor and guide team members
- Strong stakeholder and client management abilities
- Attention to detail and a compliance-focused mindset
Benefits of the Pharmacovigilance Job:
- Opportunity to work with a globally recognized consulting and technology company
- Exposure to international pharmacovigilance and regulatory projects
- Career growth in the Drug Safety and Medical Review domains
- Collaborative and inclusive workplace culture
- Opportunities for certifications, training, and skill development
- Work with advanced healthcare technologies and global clients
- Competitive professional environment with learning opportunities
- Exposure to global healthcare compliance and safety standards
- Opportunity to contribute to patient safety and regulatory excellence
