Roles & Responsibilities
• Monitor adherence to prescribed dose status across global clinical trial sites
• Identify dose discrepancies and drive timely, traceable follow-ups with sites
• Document dose-related risks and maintain inspection-ready records
• Conduct routine and ad-hoc dose surveillance reviews as per protocol
• Collaborate with Trial Managers, Clinical Medical Managers, and Medical Advisors
• Support site engagement through clear communication and data insights
• Coach site staff on dose compliance, documentation quality, and protocol adherence
• Communicate findings to trial teams and contribute to continuous improvement initiatives
Qualification
• Graduate degree in Life Sciences: M.Pharm, PharmD, Pharmacy, BDS/MDS, or MSc Nursing
Experience
• Minimum 2 years’ experience in clinical trials (Pharma/Biotech/CRO/Hospital)
• Exposure to global clinical operations and trial systems
Skills
• Strong understanding of ICH-GCP and clinical trial conduct
• Analytical mindset with ability to interpret clinical data
• Excellent communication and stakeholder management skills
• Ability to work independently in dynamic environments
• Coaching and influencing skills with strong attention to detail
About the Organisation
Novo Nordisk is a global healthcare company with a strong legacy in clinical research and innovation. Through its Global Business Services in Bangalore, the company supports worldwide clinical development with advanced risk-based monitoring, data quality, and patient safety initiatives, contributing to high-quality and compliant clinical trials across the globe.
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