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Novo Nordisk

Clinical Project Lead – Diabetes and Obesity

Novo Nordisk

Clinical Project Lead overseeing global clinical trials in diabetes and obesity at Novo Nordisk. Leading cross-functional teams to ensure trial success from start-up to completion.

Posted 7/27/2026full-timeSøborg • 🇩🇰 DenmarkSenior💰 DKK 742,600 - DKK 1,091,600 per yearWebsite

About the role

Key responsibilities & impact
  • Leading global clinical trials with full accountability for timelines, budget, risk management, and delivery of key trial milestones.
  • Driving cross-functional collaboration across trial squads, clinical operations teams, and global stakeholders to ensure efficient trial execution.
  • Lead or provide input to protocol outline and protocol development activities, ensuring timely and appropriate operational input throughout study planning.
  • Overseeing trial start-up activities, vendor selection, country allocation strategies, and inspection readiness while maintaining regulatory compliance.
  • Managing risks, resolving complex operational challenges, and ensuring clear communication with both internal and external stakeholders.
  • Act as a central project leader, creating an inspiring and collaborative environment while maintaining a strong focus on patient needs, operational feasibility, and business priorities.

Requirements

What you’ll need
  • An MSc in Natural or Health Sciences with at least 5 years of relevant experience, or a BSc combined with at least 7 years of relevant clinical development experience.
  • Significant experience leading and managing clinical trials, including planning, execution, and close-out activities.
  • Demonstrated project management expertise and experience working in complex cross-functional environments.
  • Strong communication, stakeholder management, negotiation, and influencing skills, with the ability to build trust across cultures and organisational levels.
  • A proactive mindset, strong analytical capabilities, and a solid understanding of clinical trial methodologies and regulatory requirements.
  • You work independently with minimal guidance and enjoy working in a fast-paced environment with changing priorities, sharing knowledge and insights with your colleagues.
  • Broad experience with both Clinical Pharmacology and Phase 2-4 and global trial operations will be considered a strong advantage.
  • Fluency in written and spoken English is required.

Benefits

Comp & perks
  • The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.