Job Opportunity: Analyst – Clinical Trial Transparency at GSK
Summary:
GSK is seeking a detail-oriented and experienced Analyst – Clinical Trial Transparency to join our team in Bengaluru. This critical role will contribute to ensuring the accurate and timely disclosure of clinical trial data across global platforms, supporting our commitment to transparency and regulatory compliance. If you possess a strong understanding of clinical trial operations, regulatory requirements, and data analysis, with proficiency in tools like Power BI and Excel automation, we encourage you to apply.
About GSK:
GSK is a leading global biopharma organization dedicated to researching, developing, and manufacturing innovative medicines and vaccines. Our mission is to improve the quality of human life by enabling people to do more, feel better, and live longer. We are committed to scientific excellence and ethical practices in all aspects of our operations.
About the Role:
As an Analyst – Clinical Trial Transparency, you will play a vital role in supporting the disclosure of clinical trial information to the public and regulatory bodies. You will collaborate with cross-functional teams, including regulatory, statistical, clinical, and legal departments, to ensure compliance with global transparency requirements.
Key Responsibilities:
- Maintain and update therapeutic area trackers to monitor the progress of disclosure deliverables.
- Support the creation and review of transparency deliverables, including content updates, risk assessments, and quality control checks.
- Collaborate with both internal and external teams to ensure adherence to regulatory timelines for clinical trial registration and reporting.
- Leverage tools such as Power BI, Excel automation, and Python to develop operational dashboards and streamline workflow efficiency.
- Monitor regulatory trends and adapt processes to ensure compliance with evolving requirements.
- Support the creation and maintenance of documentation, including standard operating procedures (SOPs) and training materials.
- Assist with clinical system updates, key performance indicator (KPI) reporting, and the implementation of automation-driven improvements.
- Collaborate with global matrix teams to facilitate seamless communication and ensure data transparency.
Required Qualifications:
- Master’s degree in a relevant Life Sciences field (e.g., M.Pharm, MSc, Pharm.D, Biotechnology, Clinical Research).
- Minimum of 3 years of experience in clinical trial operations or clinical data transparency.
- Strong proficiency in MS Office applications, including Word, PowerPoint, and Excel (advanced Excel skills, including formulas and macros, are preferred).
- Working knowledge of Power BI, automation workflows, or AI tools (e.g., Microsoft CoPilot).
- Programming experience, preferably with Python.
- Excellent communication and stakeholder management skills.
- Demonstrated ability to work effectively in a global, matrixed organization.
Preferred Skills:
- Experience with global regulatory disclosure platforms (e.g., ClinicalTrials.gov, EU Clinical Trial Register).
- Knowledge of the clinical trial lifecycle and associated documentation.
- Strong analytical mindset with experience in trend analysis and data interpretation.
Why Join GSK?
- Impactful Work: Contribute to clinical data transparency and responsible research communication, playing a key role in improving patient outcomes.
- Career Growth: Opportunities for professional development and advancement within regulatory affairs, clinical operations, and global healthcare systems.
- Global Leader: Work with a globally recognized leader in vaccine and specialty medicine development.
- Ethical Culture: Be part of a company committed to ethics, integrity, and scientific innovation.
- Dynamic Environment: Engage in a collaborative and challenging work environment with diverse teams.
Job Location:
Bengaluru – Luxor North Tower
Job Type:
Full-time
How to Apply:
If you are a highly motivated and skilled professional seeking a challenging and rewarding opportunity, we encourage you to apply. Please submit your resume and cover letter through our online application portal. We look forward to hearing from you.