Clinical Job at GSK | Senior Literature Specialist Role | Apply Now
GSK (GlaxoSmithKline), a global science-led healthcare company, is hiring a Senior Literature Specialist III for its Luxor North Tower hub in Bengaluru. This clinical job is a high-level pharmacovigilance role focused on global safety literature surveillance to identify potential adverse events and signals for both marketed products and those in clinical development. Pursuing a GSK Career offers the chance to join an organization driven by a culture of innovation, performance, and trust, where patient focus and transparency are at the core of all operations.
- Job Position: Senior Literature Specialist III
- Location: Bengaluru, India
- Category: Medical and Clinical
- Req ID: 433364
About the Company
GSK is a global healthcare leader with a mission to help people do more, feel better, and live longer. The company operates at pace with agile decision-making, balancing rigour and risk to deliver high-quality results. GSK’s culture is built on values of respect, integrity, and transparency, ensuring that employees have the support to sustain their energy and well-being while building strong professional relationships.
Job Overview
The primary responsibility of this role is to lead and execute the screening of global medical literature to ensure regulatory compliance and patient safety.
Key Responsibilities:
- Literature Screening: Screen and review literature search results (articles, abstracts, and citations) to identify Individual Case Safety Reports (ICSRs).
- Signal Detection Triage: Triage search results to find potential articles of interest regarding GSK products for signal detection and periodic reporting using specific algorithms.
- Quality Oversight: Demonstrate expertise in performing quality checks on literature articles triaged by junior team members.
- Search Strategy: Maintain proficiency in complex search strategy activities for robust literature surveillance.
- Process Improvement: Identify and participate in continuous process improvement activities to enhance the efficiency of literature surveillance workflows.
- Knowledge Sharing: Develop and share pharmacovigilance and literature surveillance expertise with the wider team to resolve potential issues.
Qualifications and Skills
To succeed in this GSK Career role, candidates must possess a strong foundation in drug safety and medical terminology.
Basic Qualifications:
- Industry Experience: Proven experience in the pharmaceutical industry, specifically in drug safety, regulatory affairs, clinical development, or medical affairs.
- Regulatory Knowledge: Working knowledge of key pharmacovigilance regulations and methodologies.
- Data Evaluation: Ability to evaluate scientific data and draw logical conclusions.
- Communication: Excellent English language skills, with a specific focus on scientific and medical terminology.
- Technical Proficiency: Strong IT skills and the ability to work effectively with web-based pharmacovigilance applications.
Preferred Qualifications:
- Degree: Bachelor’s Degree in Life Sciences
- Advanced Degree: A Master’s degree or higher in Health Sciences is highly preferred.
Securing a clinical job as a Senior Literature Specialist III at GSK is an elite opportunity for pharmacovigilance professionals in Bengaluru. This role is vital for maintaining the safety profile of GSK’s global portfolio, requiring a deep understanding of medical literature and regulatory standards. If you have a background in Life Sciences and experience in drug safety surveillance, this GSK Career path provides a platform for leadership and continuous professional development.
