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Sr. Associate I, Medical Literature Analyst

2+ years
Not Disclosed
10 Sept. 10, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/ B.Pharma/ M.Pharma/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Sr. Associate I, Medical Literature Analyst

📍 Location: Bangalore, India
🕒 Job Type: Full-time
📅 Posted: Yesterday
⏳ Application Deadline: October 13, 2025
🔢 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 and champion progress in global eye health. We foster an inclusive culture that values your contributions and offers unique career growth opportunities. Together, we make a difference in the lives of patients and customers.


Role Overview

Part of Alcon’s Research & Development team, the Sr. Associate I, Medical Literature Analyst supports clinical research by conducting targeted literature searches, summarizing findings, and collaborating with cross-functional teams to improve patient outcomes in eye care.


Key Responsibilities

  • Develop and execute targeted literature search strategies based on clinical protocols, product names, and other criteria to support:

    • Clinical Evaluation Reports (CERs)

    • State of the Art (SotA) reviews

    • Safety and Performance assessments

  • Conduct annual literature 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 and update relevant systems accordingly.

  • Perform process activities following Standard Operating Procedures (SOPs).

  • Maintain understanding of data requirements for technical and adverse event complaints to ensure compliance.

  • Collaborate effectively across global time zones to support international operations.

  • Review data entries and follow-up documentation for accuracy, completeness, and timeliness.

  • Stay updated on company policies, departmental procedures, and work instructions.

  • Demonstrate working knowledge of ophthalmic terminology, including eye anatomy, diseases, and procedures.

  • Proactively identify and escalate potential safety issues, emerging trends, or concerns to management.

  • Ensure adherence to corporate compliance guidelines and programs.

  • Support reconciliation activities and audits as required.


Minimum Requirements

Education:

  • Bachelor’s degree in science or healthcare field

Experience:

  • Experience in Medical Device / Pharma Complaint Handling, Device Vigilance, or Pharmacovigilance

  • Experience communicating with US-based customers

Skills:

  • Excellent listening, communication, decision-making, troubleshooting, and negotiation skills

  • Ability to manage multiple tasks with strong attention to detail and time management

  • 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

  • Strong 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.