GSK Hiring Literature Specialist Intern Pharmacovigilance Drug Safety surveillance roles.
GSK has announced a verified full-time internship opportunity for the role of Literature Specialist – Intern at its Bengaluru (Luxor North Tower) location. This role is part of GSK’s Central Safety Department (CSD) and focuses on pharmacovigilance literature surveillance, ICSR identification, and signal detection activities.
This opportunity is ideal for life sciences and pharmacy graduates who want to begin their careers in drug safety, pharmacovigilance, and medical literature review within a globally respected biopharmaceutical organization. GSK Hiring Literature Specialist Intern
About the Company
GSK is a leading global biopharma company driven by a singular purpose: to unite science, technology, and talent to get ahead of disease together. The organization aims to positively impact the health of 2.5 billion people by the end of this decade through innovative medicines and vaccines. GSK Hiring Literature Specialist Intern
GSK focuses on four core therapeutic areas:
- Respiratory, Immunology, and Inflammation
- Oncology
- HIV
- Infectious Diseases
With a strong commitment to patients, science, and ethics, GSK has built a culture centered on accountability, innovation, and integrity. Employees at GSK work in an environment that supports learning, inclusion, and professional growth while contributing to medicines and vaccines trusted by patients worldwide. GSK Hiring Literature Specialist Intern
Job Details
Company Name: GSK
Job Title: Literature Specialist – Intern
Job Requisition ID: 434037
Employment Type: Full-time Internship
Department: Central Safety Department (CSD)
Job Location: Bengaluru – Luxor North Tower
Application Deadline: January 18, 2026
Industry: Pharmacovigilance / Drug Safety / Clinical Research
Job Description
The Literature Specialist – Intern role at GSK provides hands-on exposure to global pharmacovigilance literature surveillance activities. The selected candidate will support safety monitoring for both marketed products and products under development, ensuring compliance with regulatory and internal requirements.
The intern will work closely with Safety Evaluation and Risk Management (SERM) product specialists, contributing to the identification and triaging of relevant scientific literature for Individual Case Safety Reports (ICSRs), signal detection, and periodic safety reporting.
This role offers an excellent foundation for candidates aiming to build a long-term career in drug safety, medical review, and regulatory pharmacovigilance. GSK Hiring Literature Specialist Intern
Key Responsibilities
- Provide operational support for Central Safety Department literature screening activities
- Perform pharmacovigilance literature surveillance in line with regulatory requirements and internal SOPs
- Screen scientific literature (articles, abstracts, citations) to identify potential ICSRs
- Review and triage literature search results to identify safety-relevant publications
- Identify articles containing relevant safety information related to GSK’s marketed products and products in development
- Support signal detection and periodic reporting activities using defined algorithms and criteria
- Ensure timely completion of assigned deliverables related to literature review and screening
- Maintain accuracy, consistency, and compliance in documentation and workflows
- Collaborate with SERM product specialists and internal safety teams
GSK Hiring Literature Specialist Intern
Skills / Qualifications
Educational Background (Preferred)
- Degree in Life Sciences, Pharmacy, Medicine, Biotechnology, or a related discipline
- Candidates with academic exposure to pharmacovigilance, clinical research, or medical writing will have an advantage
Technical & Professional Skills
- Strong ability to read, analyze, and interpret scientific and medical literature
- Basic understanding of pharmacovigilance and drug safety concepts
- Attention to detail and ability to identify safety-relevant information
- Good written and verbal communication skills
- Ability to work systematically with large volumes of data and publications
- Willingness to learn regulatory requirements related to ICSR and signal detection
- Ability to work effectively in a structured, process-driven environment
GSK Hiring Literature Specialist Intern
Benefits / Perks
GSK offers a supportive and growth-oriented work environment even at the internship level:
- Hands-on experience in global pharmacovigilance operations
- Exposure to real-world drug safety and literature surveillance processes
- Opportunity to work with experienced safety and risk management professionals
- Structured learning in regulatory-compliant pharmacovigilance activities
- Strong brand value and career foundation in the biopharma industry
- Inclusive and ethical workplace culture
GSK Hiring Literature Specialist Intern
Why You Should Join
Joining GSK as a Literature Specialist – Intern allows you to work at the intersection of science, patient safety, and global healthcare impact. This role provides a unique opportunity to understand how safety information from scientific literature contributes to regulatory decision-making and patient protection worldwide. GSK Hiring Literature Specialist Intern
GSK’s strong emphasis on ethics, inclusion, and scientific excellence makes it an ideal organization for early-career professionals who want meaningful exposure and long-term career potential in pharmacovigilance and drug safety.
Inclusion & Equal Opportunity
GSK is an equal opportunity employer committed to inclusion and accessibility. Candidates who require any adjustments during the recruitment process are encouraged to reach out to:
Email: IN.recruitment-adjustments@gsk.com
GSK ensures a workplace free from discrimination and harassment, where individuals can thrive regardless of background.
Important Notice on Recruitment Fraud
GSK does not charge any fees at any stage of the recruitment process. Candidates are advised to be cautious of fraudulent job advertisements or emails requesting payments. GSK Hiring Literature Specialist Intern
- Official communication will only come from email addresses ending with @gsk.com
- Any suspicious emails or advertisements should be reported to askus@gsk.com
FAQs
Is this a full-time role?
Yes, this is a full-time internship position.
Is prior pharmacovigilance experience required?
Prior experience is not mandatory, but basic knowledge of drug safety or literature review is an advantage.
Where is the job located?
The role is based at GSK’s Bengaluru (Luxor North Tower) office.
What is the last date to apply?
The application deadline is January 18, 2026.
Does GSK accept agency referrals?
No, GSK does not accept referrals from recruitment agencies without prior written authorization.
How to Apply
Interested candidates should apply online through the official GSK careers portal before January 18, 2026, using Job Requisition ID: 434037.
This is a strong entry-level opportunity to begin your career in pharmacovigilance and medical safety with one of the world’s leading biopharmaceutical companies.
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
