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Pharmacovigilance Services Assoc Manager

Accenture
10-14 years
INR 15 LPA – 25 LPA
Bangalore, India
1 June 12, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

Job Title: Pharmacovigilance Services Associate Manager
Company: Accenture
Location: Bengaluru
Job Type: Full-Time
Experience Required: 10–14 Years
Qualification: MBA / M.Pharm

About the Role
Accenture is hiring a Pharmacovigilance Services Associate Manager to lead pharmacovigilance operations, project governance, MIS reporting, compliance monitoring, resource planning, and client management activities. The role requires strong leadership capabilities, operational oversight, regulatory compliance expertise, and stakeholder management experience within global drug safety programs.

Key Responsibilities

Pharmacovigilance Operations Management

  • Oversee end-to-end pharmacovigilance and drug safety surveillance activities.

  • Ensure smooth execution of ICSR processing, case management, submissions, and follow-up activities.

  • Monitor project deliverables and ensure adherence to client requirements.

Project & Resource Management

  • Forecast workload and support resource planning activities.

  • Manage service delivery timelines and project milestones.

  • Define and maintain project management standards, methodologies, and operational processes.

  • Ensure optimal resource utilization across projects.

MIS Reporting & Analytics

  • Prepare daily, weekly, monthly, and annual operational reports.

  • Develop dashboards and performance monitoring tools.

  • Analyze operational metrics and identify improvement opportunities.

  • Present project performance updates to management and clients.

Quality & Compliance

  • Ensure compliance with SOPs, regulatory requirements, SLAs, KPIs, and quality standards.

  • Support audits, inspections, CAPA management, and quality improvement initiatives.

  • Monitor project outcomes through statistical analysis and trend evaluation.

  • Implement preventive and corrective actions where necessary.

Client & Stakeholder Management

  • Act as a key point of contact for clients and internal stakeholders.

  • Provide regular updates on project performance and operational metrics.

  • Manage escalations and ensure timely issue resolution.

  • Build strong client relationships and maintain service excellence.

Team Leadership

  • Lead, mentor, and develop medium-sized pharmacovigilance and MIS teams.

  • Drive employee engagement, productivity, and performance improvement initiatives.

  • Support training, knowledge sharing, and continuous learning programs.

  • Foster a culture of operational excellence and compliance.

Required Skills

  • Pharmacovigilance Operations Management

  • Drug Safety Surveillance

  • ICSR Lifecycle Management

  • Team Leadership & People Management

  • Resource Planning

  • MIS Reporting & Dashboard Development

  • Quality Management Systems

  • Regulatory Compliance

  • Client Relationship Management

  • Project Management

  • Risk Assessment & Escalation Management

  • Data Analytics & Performance Monitoring

Preferred Qualifications

  • Experience in global pharmacovigilance operations within CRO, BPO, or pharmaceutical organizations.

  • Strong understanding of FDA, EMA, MHRA, ICH, and GVP guidelines.

  • Experience with safety databases such as Argus Safety, ArisG, or PV-Works.

  • Knowledge of audit readiness, CAPA management, and compliance frameworks.

  • Exposure to business intelligence and reporting tools.