Job Title:
Manager I, Medical Literature Review
📍 Location: Bangalore, India
🕒 Job Type: Full-time
📅 Posted: Yesterday
⏳ Application Deadline: October 13, 2025
🔢 Job Requisition ID: R-2025-42062
Company Overview
At Alcon, we are passionate about enhancing sight and helping people see brilliantly. With over 25,000 associates globally, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture that values your contributions and provides opportunities for career growth. Together, we make a difference in the lives of our patients and customers.
Role Overview
This role is part of Alcon’s Research & Development function. The Manager I will lead the Medical Literature Analyst team, ensuring quality, compliance, and efficient stakeholder management while overseeing routine and on-demand literature search activities that support clinical and regulatory functions.
Key Responsibilities
Lead and manage the Medical Literature Analyst team:
Provide direction, prioritize activities, and support professional development.
Foster a collaborative, high-performance work environment.
Develop and execute targeted literature search strategies based on clinical protocols, product names, and relevant criteria to support:
Clinical Evaluation Reports (CERs)
State of the Art (SotA) reviews
Safety and Performance assessments
Conduct annual queries for clinical and non-clinical reports in collaboration with Regulatory Affairs.
Provide literature support for Medical Safety, Complaint Intake, Medical Information, and Health Economics & Outcomes Research (HEOR).
Summarize publications to identify new complaints or risks, updating relevant systems accordingly.
Liaise with vendors and publishers to resolve technical issues and communicate service-impacting changes organization-wide.
Manage acquisition and analysis of usage data to guide journal selection and subscription decisions.
Retrieve full-text articles to ensure uninterrupted access for requested literature.
Develop and deliver training sessions to enhance end-user proficiency with knowledge center tools and resources.
Provide usage reporting to the Copyright Clearance Center to ensure licensing compliance.
Respond promptly to inquiries via the Ask AKC mailbox, supporting internal stakeholders.
Execute process activities in accordance with Standard Operating Procedures (SOPs).
Maintain understanding of data requirements for technical and adverse event complaints ensuring compliance.
Collaborate across global time zones to support international operations.
Review data entry and documentation for accuracy and timeliness.
Stay updated with company policies, procedures, and compliance guidelines.
Demonstrate knowledge of ophthalmic terminology, eye anatomy, diseases, and procedures.
Proactively identify and escalate potential safety issues, trends, or concerns to management.
Support reconciliation activities and audits as required.
Minimum Qualifications
Education:
Bachelor’s degree in science or healthcare field
Experience:
3-5 years relevant work experience in device/drug safety, compliance, quality assurance, or data analytics
Proven experience managing direct reports
Experience communicating with US-based customers
Experience in Medical Device / Pharma Complaint Handling, Device Vigilance, or Pharmacovigilance
Skills:
Strong leadership skills with the ability to influence senior leadership
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 guidelines
Understanding of medical device safety and vigilance in pre- and post-marketing contexts
Basic proficiency in MS Office
Excellent written and verbal communication skills
Additional Information
Current Alcon Employees/Contingent Workers: Please apply via the internal career site using the appropriate links provided.
Alcon is an Equal Opportunity Employer committed to diversity and inclusion in all employment practices.
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China | Quarry Bay |Hubei :
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Sofia |Canada :
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Richmond Hill | Renfrew | Mississauga | Uxbridge | North York | Australia |Quebec :
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