Assistant Manager – Pharmacovigilance, Epidemiology & Risk Management
Location: Noida, India
Employment Type: Full-Time
Category: Consulting
Job ID: R26161
Posted Date: 20 January 2026
Affiliated Company: PharmaLex India Private Limited (A Cencora Company)
About Cencora
Cencora is a global healthcare solutions organization dedicated to creating healthier futures for people and animals worldwide. Driven by innovation, compliance excellence, and scientific rigor, Cencora empowers its teams to deliver impactful solutions across the healthcare ecosystem. Joining Cencora means becoming part of a purpose-driven organization where every role contributes to improving lives globally.
Role Overview
The Assistant Manager – Pharmacovigilance, Epidemiology & Risk Management is a leadership-focused role responsible for managing pharmacovigilance operations, ensuring regulatory compliance, and overseeing team performance across global PV projects. This position combines hands-on case processing expertise with people management, quality oversight, client interaction, and audit readiness.
The role is ideal for an experienced pharmacovigilance professional with strong regulatory knowledge, leadership capabilities, and a commitment to patient safety.
Key Responsibilities
Pharmacovigilance Operations & Case Management
Perform triage and initial validity assessment of Individual Case Safety Reports (ICSRs), including spontaneous, clinical trial, health authority, and literature cases
Conduct case processing activities including data entry, quality control (QC), case completion, and documentation
Evaluate the need for expedited reporting and ensure adherence to regulatory reporting timelines
Prepare and submit standard safety reporting forms such as CIOMS I, MedWatch forms, and XML files
Generate and manage follow-up requests and submit ICSRs to Health Authorities and client partners
Quality, Compliance & Risk Management
Oversee quality management, workload distribution, documentation, and compliance for assigned PV projects
Ensure compliance with internal SOPs and external national and international pharmacovigilance regulations
Prepare, review, and maintain PV quality documents including SOPs, Working Instructions, SDEAs, templates, and project metafiles
Organize and conduct training on PV procedures and quality documentation
Represent the Pharmacovigilance department during client audits and regulatory authority inspections
Leadership & People Management
Act as line manager for assigned pharmacovigilance staff
Manage project coordination, staffing, and resource allocation across PV projects
Lead recruitment activities for the PV department
Conduct goal setting, performance reviews, and annual appraisals, providing structured feedback and development guidance
Ensure training compliance and up-to-date CVs, job descriptions, and training records for all team members
Mentor new joiners, supporting onboarding and fostering a collaborative learning environment
Client & Business Support
Serve as a client contact point for assigned PV projects and support cross-functional project management activities
Ensure timely generation and sharing of monthly invoices for PV clients
Support additional service lines and responsibilities as required, aligned with qualifications and business needs
Education & Experience
Education
University degree in Life Sciences or a related discipline
Experience Required
Minimum 5 years of hands-on experience in Pharmacovigilance, with strong exposure to global PV regulations
Demonstrated experience in case processing, expedited reporting, quality management, and audit readiness
Prior experience in team leadership or supervisory roles is highly desirable
Key Skills & Competencies
Strong written and verbal communication skills with the ability to identify issues and propose effective solutions
Sound knowledge of global pharmacovigilance regulations and reporting standards
Excellent organizational and workload management skills
Ability to manage multiple priorities in a regulated, fast-paced environment
Leadership mindset with a focus on mentoring, compliance, and continuous improvement
What Cencora Offers
Cencora provides a supportive and inclusive work environment with competitive benefits aligned to local market practices. Employees benefit from opportunities for professional growth, global exposure, and meaningful contributions to patient safety and public health.
Equal Employment Opportunity
Cencora is an equal opportunity employer committed to diversity, equity, and inclusion. Employment decisions are made without regard to race, color, religion, sex, sexual orientation, gender identity, age, disability, veteran status, or any other legally protected characteristic.
Reasonable accommodations are available for qualified individuals with disabilities during the recruitment process.
Apply now on thepharmadaily.com
Advance your career in Pharmacovigilance and Risk Management with a global healthcare leader.
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