Novo Nordisk A/S in the UK is seeking a Start Up Specialist to deliver regulatory, ethics and national approvals for clinical trials managed by the CDC UK. You will collaborate with the Start Up Trial Manager and Trial Squad to secure site approvals and ensure timely site activation in line with UK regulations and Novo Nordisk SOPs.
You will lead submissions via IRAS, manage cost negotiations with Trusts/Boards and GP sites, and coordinate amendments while maintaining quality and compliance
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UK Clinical Trial Start-Up Specialist employer: Novo Nordisk A/S
At Novo Nordisk, we pride ourselves on being an exceptional employer, offering a dynamic work environment in Gatwick that fosters collaboration and innovation. Our commitment to employee growth is evident through abundant learning opportunities and a culture that values diverse perspectives, ensuring that every team member contributes to our mission of improving health for millions globally. Join us to be part of a legacy that not only focuses on defeating chronic diseases but also prioritises your career development and well-being.
