About GSK
GSK (GlaxoSmithKline) is a global biopharmaceutical company driven by its mission to unite science, technology, and talent to tackle diseases worldwide. With a strong focus on innovation, GSK aims to improve the health of billions by advancing solutions in vaccines, specialty medicines, and general healthcare. At GSK, employees thrive in a culture of inclusivity, growth, and innovation, making it a prime destination for professionals seeking meaningful and impactful careers.Key Responsibilities
As a Pharmacovigilance Literature Specialist, your role will encompass: Key Responsibilities: Core Activities- Provide support for Global Safety literature screening activities for both ICSR and signal detection purposes in accordance with their procedures and regulatory requirements.
- Support SERM product specialists by identifying articles of interest for relevant safety information from screened publications for all of GSK’s product portfolio.
- Perform PV literature surveillance activities according to regulations and agreed processes
- Ensure timely production of key deliverables including but not limited to:
- Screen and review literature search results (articles/abstracts/citations) for purposes of ICSR identification
- 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 Master drug list.
- Demonstrate working knowledge in quality checks for literature articles triaged by team.
- 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, the expertise and ability to work with web-based applications
- Good level of flexibility and ability to prioritize work
- Good/Highly developed interpersonal, presentation and communication skills.
Qualifications and Skills
Educational Requirements:- Mandatory: Bachelor’s Degree in Life Sciences, Pharmacy, Pharmacology, or related fields.
- Preferred: Master’s Degree or higher in Health Sciences.
- 2-4 years of experience in the pharmaceutical industry, with exposure to pharmacovigilance, regulatory affairs, or medical affairs.
- Familiarity with pharmacovigilance regulations and methodologies.
- Strong analytical and communication skills, with proficiency in medical and scientific terminology.
- Expertise in handling web-based applications and data evaluation tools.
Job Details
- Job Title: Pharmacovigilance Literature Specialist
- Location: Bangalore, India
- Experience Level: 2-4 years
- Job Type: Full-time
- Department: Medical and Clinical
[caption id="attachment_111627" align="aligncenter" width="1200"] GSK Hiring Pharmacovigilance Literature Specialist Recruitment[/caption]
How to Apply
Take the next step in your career by applying for this exciting opportunity with GSK. Click the link below to submit your application: Apply for GSK Pharmacovigilance Literature Specialist Application Deadline: Rolling applications—apply soon to avoid missing out!Important Notes
- GSK does not charge any fees during the recruitment process. Be cautious of fraudulent job postings and verify information through official channels.
- If you have questions or concerns, contact askus@gsk.com for confirmation regarding the job’s authenticity.