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Sr. Associate I, Medical Literature Analyst

0-2 years
Not Disclosed
10 Sept. 15, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.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

Employment Type:

Full-time

Job Requisition ID:

R-2025-42064

Application Deadline:

October 13, 2025


Company Overview:

Alcon is dedicated to enhancing sight and helping people see brilliantly. With over 25,000 associates, Alcon drives innovation in eye care, promotes optimal patient outcomes, and fosters an inclusive, collaborative culture.


Role Summary:

The Sr. Associate I, Medical Literature Analyst is part of Alcon’s Research & Development function. This role is responsible for:

  • Conducting routine and on-demand literature searches for the Alcon Knowledge Center.

  • Supporting internal stakeholders by refining search strategies to improve the relevance and quality of retrieved publications.

  • Summarizing reported adverse events and complaint records to support regulatory and clinical decision-making.


Key Responsibilities:

  1. Literature Search & Analysis

    • Develop and execute targeted literature search strategies based on clinical protocols, product names, and other relevant criteria.

    • Support the preparation of Clinical Evaluation Reports (CERs), State of the Art (SotA) reviews, and Safety & Performance assessments.

    • Conduct annual queries for clinical and nonclinical reports in collaboration with Regulatory Affairs.

  2. Medical & Safety Support

    • Provide literature support for Medical Safety, Complaint Intake, Medical Information, and HEOR teams.

    • Perform summarization and analysis to identify new complaints/risks and add to appropriate systems.

    • Ensure compliance with company SOPs and global medical device regulations.

  3. Data Management & Compliance

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

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

    • Ensure adherence to corporate compliance guidelines, policies, and work instructions.

  4. Collaboration & Communication

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

    • Identify and escalate potential safety issues, emerging trends, or areas of concern to management.

  5. Professional Knowledge

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

    • Provide support for reconciliation activities and audits as needed.


Minimum Qualifications:

  • Bachelor’s degree in science or healthcare field.

  • Experience in Medical Device / Pharma Complaint Handling / Device Vigilance / Pharmacovigilance.

  • Experience communicating with US-based customers.

  • Excellent listening, 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.

  • Basic knowledge of MS Office.

  • Excellent written and verbal communication skills.


Additional Information:

  • Current Alcon employees or contingent workers should apply via the internal career site.

  • Alcon is an equal opportunity employer, committed to maintaining a diverse and inclusive workplace.