BPharma Jobs GSK | Pharmacy Graduates Apply Now at GSK
GSK is hiring a Senior Scientist in Safety Evaluation and Risk Management (SERM) at its Bengaluru Luxor North Tower site. This role offers an exciting opportunity for pharmacy professionals passionate about patient safety and global health. As a key member of GSK’s safety team, you will evaluate safety risks, contribute to regulatory documentation, and collaborate with cross-functional teams to ensure compliance with international standards.
- Role: SERM Senior Scientist
- Job ID: 427524
- Location: Bengaluru, India
- Site: Luxor North Tower
- Department: Medical and Clinical
About GSK:
GSK is a global biopharma company focused on uniting science, technology, and talent to advance global health. With a commitment to positively impacting the health of 2.5 billion people by the end of the decade, GSK aims to prevent and treat diseases through innovation in specialty medicines and vaccines. The company’s therapeutic areas include respiratory, immunology, oncology, HIV, and infectious diseases.
Education:
BPharm or advanced degree (Master’s, PhD, PharmD)
Experience:
- Familiarity with safety databases and tools.
- Experience in pharmacovigilance, safety surveillance, or drug development.
- Knowledge of global regulatory requirements and safety data management.
- Strong analytical and communication skills.
- Ability to work effectively in a matrix environment.
- Experience in drafting aggregate safety documents and risk management plans.
Job Description
As a Senior Scientist in SERM at GSK, you will play a pivotal role in monitoring and evaluating the safety of GSK’s products. This includes ensuring compliance with global regulatory standards, identifying safety signals, and drafting regulatory documents. The role requires strong collaboration across cross-functional teams to address safety-related issues and provide critical input on safety documentation.
Responsibilities:
- Responsible for safety monitoring and evaluation of assigned GSK products.
- Conduct safety monitoring and evaluation for assigned products, including signal detection and risk assessment.
- Review and analyze individual case safety reports (ICSRs) and literature for safety signals.
- Draft and contribute to regulatory documents, including periodic safety reports and risk management plans.
- Collaborate with cross-functional teams to address safety-related queries and ensure compliance with regulatory requirements.
- Provide input on labeling updates and safety-related documentation.
- Mentor junior colleagues and contribute to process improvement initiatives within the safety team.
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