GSK Hiring Literature Specialist I Pharmacovigilance in Bengaluru for pharmacovigilance safety literature screening and global drug safety support role.
Company Overview
GlaxoSmithKline (GSK) is a leading global biopharmaceutical organization focused on discovering, developing, and delivering innovative vaccines and medicines. With a strong emphasis on science-led research, advanced technology, and patient-centric outcomes, GSK works across multiple therapeutic areas to improve health at scale. The company fosters a collaborative and inclusive work culture that prioritizes integrity, accountability, and continuous learning. GSK Hiring Literature Specialist I
As part of its expanding global safety and medical operations, GSK is hiring a Literature Specialist I to support pharmacovigilance literature surveillance activities from its Bengaluru location.
Job Location & Employment Type
- Job Location: Bengaluru, Karnataka
- Employment Type: Full-Time
- Work Mode: On-site / Hybrid (as per business requirement)
- Industry: Pharmacovigilance | Drug Safety | Medical Affairs
- Job Level: Entry to Mid-Level
Open Positions / Department Details
Position Title: Literature Specialist I
Department: Global Safety / Pharmacovigilance
Job Requisition ID: 435262
Experience Required: 1 to 5 Years
This role supports global safety teams by ensuring accurate and timely review of scientific and medical literature relevant to product safety. GSK Hiring Literature Specialist I
Key Roles & Responsibilities
The Literature Specialist I will play a key role in pharmacovigilance literature monitoring and safety surveillance activities. GSK Hiring Literature Specialist I
Primary Responsibilities Include:
- Supporting global safety literature screening activities for ICSR identification and signal detection
- Conducting pharmacovigilance literature surveillance in line with regulatory requirements and internal procedures
- Screening and reviewing scientific literature, abstracts, citations, and publications
- Identifying potential adverse event information related to marketed and pipeline products
- Triaging literature for safety relevance using predefined criteria and algorithms
- Supporting signal detection and periodic safety reporting activities
- Maintaining accurate and up-to-date product knowledge for literature assessment
- Managing and referencing the master drug list during literature reviews
- Performing quality checks on screened and triaged literature
- Documenting literature review activities in compliance with audit requirements
- Collaborating with global safety, medical affairs, and regulatory teams
- Demonstrating company values through accuracy, integrity, and teamwork
Eligibility Criteria
Education
Candidates must possess a Bachelor’s degree in one of the following disciplines:
- Life Sciences
- Pharmacy
- Pharmacology
- Medical or related scientific fields
Experience
- 1 to 5 years of experience in one or more of the following areas:
- Scientific or medical literature searching
- Pharmacovigilance support
- Medical writing
- Drug safety, regulatory, clinical development, or medical affairs roles
Skills Required
- Working knowledge of pharmacovigilance regulations and safety methodologies
- Strong understanding of medical and scientific terminology
- Experience in literature searching, screening, and data evaluation
- High attention to detail and strong quality focus
- Ability to analyze data and draw conclusions with appropriate guidance
- Proficiency in web-based applications and IT systems
- Excellent written and verbal English communication skills
- Strong interpersonal skills with the ability to work in cross-functional teams
- Flexible approach to work and ability to prioritize tasks effectively
- Service-oriented mindset and collaborative working style
GSK Hiring Literature Specialist I
Salary & Benefits
- Salary: As per company norms
GSK offers a competitive compensation package along with learning and development opportunities, exposure to global safety operations, and a supportive work culture focused on professional growth and patient safety. GSK Hiring Literature Specialist I
Selection Process
- Online application screening
- Technical and functional interview
- Evaluation of pharmacovigilance and literature review knowledge
- Final HR discussion
Selection will be based on experience relevance, technical competency, and alignment with company values.
How to Apply
Mode of Application: Online Application
Interested candidates should apply through the official GSK careers portal before the application deadline.
Application Deadline: February 20, 2026
Candidates requiring workplace or recruitment adjustments may contact:
Email: IN.recruitment-adjustments@gsk.com
Important Dates
- Last Date to Apply: February 20, 2026
Why Apply for This Pharma Job?
This role offers a strong entry point into global pharmacovigilance and literature surveillance within a reputed biopharmaceutical organization. Candidates will gain exposure to international safety processes, regulatory standards, and cross-functional collaboration. It is an excellent opportunity for professionals seeking to build a long-term career in drug safety, medical affairs, and regulatory science while contributing to patient protection. GSK Hiring Literature Specialist I
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with GSK or its recruitment partners. GSK does not charge any fees at any stage of the recruitment process. Candidates are advised to apply only through official company channels and verify job authenticity before proceeding. GSK Hiring Literature Specialist I
Final Call-to-Action
Qualified professionals with experience in scientific literature review and pharmacovigilance are encouraged to apply before the deadline to join GSK’s global safety team. GSK Hiring Literature Specialist I
