GSK (GlaxoSmithKline) is a global biopharmaceutical leader dedicated to uniting science, technology, and talent to get ahead of disease together. With a commitment to improving global health, GSK focuses on four core therapeutic areas: infectious diseases, HIV, respiratory/immunology, and oncology. Through innovative research and advanced technologies, GSK prevents and treats diseases, positively impacting billions of lives worldwide. As a people-centric organization, GSK fosters a workplace where employees feel inspired, valued, and empowered to thrive.
If you’re a skilled writer with a passion for clinical and regulatory documentation, this Medical Writer position at GSK Bengaluru offers a platform to grow your career while contributing to groundbreaking healthcare innovations.
Responsibilities in the Role
As a Medical Writer at GSK, you will play a crucial role in ensuring the delivery of high-quality clinical and regulatory documents. Your key responsibilities include:
- Document Creation and Review:
- Author clinical and regulatory documents such as protocols, clinical study reports (CSR), and modules (M2 & M5) following defined templates.
- Ensure consistency and maintain high-quality standards for all deliverables.
- Collaboration and Coordination:
- Work under the guidance of a mentor or independently to coordinate with stakeholders for efficient execution of assignments.
- Participate in planning and review meetings, fostering effective communication with the global Medical Writing Team.
- Content Expertise:
- Interpret and communicate clinical data clearly and succinctly.
- Understand and apply statistical principles and scientific methodologies in clinical research.
- Problem-Solving and Initiative:
- Proactively identify and discuss issues, proposing effective solutions.
- Promote high medical writing standards by pointing out flaws and suggesting alternatives.
Qualifications
To succeed in this role, you should meet the following educational and experiential qualifications:
- Educational Requirements:
- MSc in Life Sciences or MPharm.
- Experience:
- Up to 2 years of writing experience in the pharmaceutical industry is advantageous.
Skills and Expertise
- Strong understanding of clinical research methodologies and ICH/GCP guidelines.
- Proficiency in interpreting, analyzing, and documenting clinical data.
- Excellent English language skills, both written and verbal.
- Attention to detail and ability to work with consistency in a dynamic, matrix organization.
- Good computer literacy and familiarity with statistical principles in clinical research.
