Medical Job at GSK in Bangalore | Apply Now
If you are looking for a rewarding Medical Job in the pharmaceutical industry, GSK Careers presents an excellent opportunity for a Literature Specialist in Bangalore, India. This full-time position within GSK Jobs offers professionals the chance to contribute to global safety literature monitoring, pharmacovigilance activities, and regulatory compliance while advancing their scientific expertise in a dynamic and innovation-driven environment.
Job Details:
- Position: Literature Specialist
- Location: Bangalore, India
- Type: Full-time
- Category: Medical and Clinical Literature Specialist
- Job ID: 435262
- Site Name: India – Karnataka – Bengaluru
About the Company
GSK has bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Research and Development focuses on discovering and delivering vaccines and medicines, combining understanding of the immune system with cutting-edge technology to transform lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, ensuring focus on accelerating significant assets that meet patients’ needs and have the highest probability of success. Science, technology, and talent are united to get ahead of disease together.
Job Description
This Medical Job supports literature monitoring and review activities that help keep safety and medical teams informed. The Literature Specialist 1 works closely with pharmacovigilance, medical affairs, and regulatory teams. The role emphasizes accuracy, scientific evaluation, and clear communication. It offers opportunities to grow scientific knowledge, develop skills in literature searching and screening, and contribute to safety decisions that protect patients. Candidates exploring GSK Jobs and GSK Careers in Bangalore will find this position aligned with global pharmacovigilance standards.
Qualifications
- 1–5 years’ experience in scientific literature searching, medical writing, or pharmacovigilance support.
- Bachelor’s Degree – Medical or pharmacology degrees.
- Pharmaceutical industry experience (e.g., drug safety (desired), regulatory, clinical development, medical affairs).
- Working knowledge of key pharmacovigilance regulations and methodologies.
- Good English language skills – written and verbal, particularly in scientific/medical terminology.
- Ability to evaluate data and draw conclusions with appropriate guidance from senior team members or manager.
- Good attention to detail.
- Service-oriented attitude and ability to be a team player and interact effectively with all levels of personnel in an interdisciplinary and matrix environment.
- Computer proficiency, IT skills, and the ability to work with web-based applications.
- Good level of flexibility and ability to prioritize work.
- Good/Highly developed interpersonal, presentation, and communication skills.
Key Responsibilities
- Provide support for Global Safety literature screening activities for both ICSR and signal detection purposes in accordance with their procedures and regulatory requirements.
- Perform PV literature surveillance activities according to regulations and agreed processes.
- Ensure timely production of key deliverables, including: Screen and review literature search results (articles/abstracts/citations) for purposes of ICSR identification and Triage literature search results for potential articles of interest with relevant safety information concerning both GSK-marketed and GSK products in development, for signal detection/periodic reporting purposes using defined algorithms and criteria.
- Demonstrate GSK values.
- Maintain and document up-to-date product knowledge for literature review.
- Possess working knowledge of the maintenance of product knowledge and the Master Drug List.
- Demonstrate working knowledge of quality checks for literature articles triaged by the team.
