FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Clinical Project Lead – Diabetes and Obesity
Novo NordiskClinical 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.
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.