Specialist – Case Processing (Pharmacovigilance)
Job ID: R26668
Location: Noida, India
Employment Type: Full-Time
Category: Consulting / Pharmacovigilance
Experience Required: Minimum 2 Years
Date Posted: January 19, 2026
Job Overview
Cencora is seeking a highly skilled Specialist – Case Processing to support global pharmacovigilance operations through accurate processing, assessment, and reporting of Individual Case Safety Reports (ICSRs). This role is critical in ensuring regulatory compliance, data integrity, and timely safety reporting across spontaneous, clinical trial, literature, and health authority cases.
The position offers an opportunity to work within a globally integrated pharmacovigilance environment while contributing directly to patient safety and regulatory excellence.
Key Responsibilities
Perform triage and initial validity assessment of safety cases, including spontaneous, clinical trial, literature, and health authority reports
Conduct accurate data entry into pharmacovigilance safety databases
Perform initial ICSR assessment and determine case completeness and reportability
Evaluate the need for expedited reporting to health authorities and business partners in accordance with regulatory timelines
Prepare standard regulatory reporting forms, including CIOMS I, MedWatch forms, and XML submissions
Generate, send, and track follow-up requests to obtain additional safety information
Submit ICSRs to global health authorities and client partners within defined timelines
Complete case documentation and ensure end-to-end case lifecycle management
Conduct quality checks of ICSRs to ensure compliance with project requirements, industry standards, and best practices
Perform ICSR search and retrieval activities from EVWEB and assess company versus non-company cases
Support onboarding and mentoring of new team members by providing guidance on processes and best practices
Ensure adherence to internal SOPs, regulatory guidelines, and pharmacovigilance compliance standards
Execute additional responsibilities as assigned by the supervisor in line with operational requirements
Required Qualifications
University degree in Life Sciences or a related discipline
Minimum 2 years of hands-on experience in pharmacovigilance case processing
Strong understanding of global pharmacovigilance regulations and safety reporting requirements
Required Skills and Competencies
Strong written and verbal communication skills
Ability to identify issues within safety cases and propose appropriate resolution options
High attention to detail and strong data quality orientation
Ability to work effectively in a regulated, process-driven environment
Experience working with pharmacovigilance databases and safety reporting tools
Collaborative mindset with the ability to mentor and support junior team members
About Cencora
Cencora is a global healthcare services organization dedicated to creating healthier futures by improving access to therapies and enhancing patient outcomes. Through innovation, collaboration, and deep industry expertise, Cencora supports pharmaceutical, biotech, and healthcare partners across the product lifecycle.
Equal Employment Opportunity
Cencora is an equal opportunity employer committed to providing a workplace free from discrimination and harassment. Employment decisions are based on qualifications, experience, and business needs without regard to race, religion, gender, sexual orientation, age, disability, veteran status, or any other legally protected status.
Reasonable accommodations are provided to qualified individuals during the employment process in accordance with applicable laws.
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