Role & Responsibilities
• Oversee adherence to prescribed dose status across assigned clinical trial sites
• Identify prescribed vs expected dose discrepancies and drive traceable follow-ups
• Collaborate with Clinical Medical Managers and Medical Advisors on dose-related issues
• Document dose-related operational risks and maintain inspection-ready records
• Execute routine and ad-hoc dose surveillance reviews as per protocol requirements
• Support site engagement through clear communication and timely escalation
• Partner with Trial Managers on dose and retention-related matters
• Coach site staff on dose compliance, documentation quality, and protocol adherence
• Communicate findings to trial squads and medical partners for informed decisions
• Contribute to continuous improvement and development of surveillance processes
Qualification
• Graduate degree in Life Sciences (M.Pharm, PharmD, Pharmacy, BDS/MDS, MSc Nursing)
• Strong understanding of clinical trial conduct and ICH-GCP
Experience
• Minimum 2 years’ experience in clinical trials (pharma/biotech/CRO/hospital)
• Strong knowledge of clinical trial data, systems, and global operations
• Experience working with cross-functional and global stakeholders
Skills
• Excellent communication and relationship-building skills
• Strong analytical and problem-solving abilities
• Familiarity with clinical IT systems and trial tools
• Ability to work independently in dynamic environments
• High ownership, motivation, and continuous improvement mindset
• Ability to coach, influence, and manage stakeholders effectively
About the Company
• Novo Nordisk is a global healthcare company with over 100 years of innovation , Strong focus on patient safety, clinical quality, and data integrity
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