Sr. Associate I – Medical Literature Analyst
Location: Bangalore, India
Employment Type: Full-time
Application Deadline: October 13, 2025 (27 days left)
Job Requisition ID: R-2025-42064
Company Overview
At Alcon, we are passionate about enhancing sight and helping people see brilliantly. With over 25,000 associates worldwide, we:
Innovate fearlessly
Champion progress
Act swiftly to impact global eye health
We foster an inclusive culture, recognizing contributions and providing opportunities for career growth.
Function
This role is part of Alcon’s Research & Development function, which focuses on:
Innovating new products and services
Advancing optimal patient outcomes
Driving excellence in eye care
Role Summary
The Sr. Associate I is primarily responsible for:
Conducting routine and on-demand literature search activities for the Alcon Knowledge Center
Supporting internal stakeholders by refining search strategies to enhance relevance and quality of retrieved publications
Providing concise summaries of reported adverse events (AEs) and complaint records to aid regulatory and clinical decision-making
Major Accountabilities
Literature Searches:
Develop and execute targeted literature search strategies based on clinical protocols, product names, and other relevant criteria
Support Clinical Evaluation Reports (CERs), State of the Art (SotA) reviews, and Safety and Performance assessments
Regulatory Collaboration:
Conduct annual queries for clinical and nonclinical reports in collaboration with Regulatory Affairs
Medical Safety Support:
Provide literature support for Medical Safety and Complaint Intake
Support ad-hoc search requests from Medical Information and Health Economics and Outcomes Research (HEOR) teams
Data Analysis:
Summarize and analyze publications to identify new complaints or risks, and update relevant systems
Review data entry and follow-up documentation for accuracy, completeness, and timeliness
Compliance & SOPs:
Execute process activities in accordance with established Standard Operating Procedures (SOPs)
Ensure adherence to corporate compliance guidelines
Collaboration & Communication:
Collaborate effectively across global time zones to support international operations
Proactively identify and escalate potential safety issues, emerging trends, or areas of concern
Knowledge Management:
Maintain a strong understanding of data requirements for technical and AE complaints
Demonstrate working knowledge of ophthalmic terminology, including eye anatomy, common diseases, and procedures
Provide support for reconciliation activities and audits as needed
Minimum Requirements
Education: Bachelor’s degree in Science or Healthcare field
Experience:
Medical Device / Pharma Complaint Handling / Device Vigilance / Pharmacovigilance
Communicating with US-based customers
Skills:
Excellent listening, communication, decision-making, troubleshooting, and negotiation skills
Ability to manage multiple tasks, prioritize work, and maintain attention to detail
Knowledge of national and international medical device regulations and regulatory guidelines
Knowledge of medical device safety and vigilance in pre- and post-marketing practices
Basic proficiency in MS Office
Excellent written and verbal communication skills
Notes
Current Alcon Employees/Contingent Workers: Apply via the Internal Career site.
Equal Opportunity: Alcon maintains a diverse environment and does not discriminate based on race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital status, disability, or any other reason.
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