Novo Nordisk in United Kingdom is seeking a Start Up Specialist to deliver regulatory, ethics and national approvals for UK clinical trials. You will partner with the Start Up Trial Manager to negotiate site contracts, secure approvals and activate sites in line with UK rules and Novo Nordisk standards.
The role requires experience in regulatory submissions (HRA, MHRA, REC), SOPs, and strong IT system proficiency (IRAS, CPMS, Coupa). A degree and GCP training are beneficial.
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UK Clinical Trial Start-Up Specialist employer: Novo Nordisk
At Novo Nordisk, we are dedicated to making a meaningful impact in the field of rare blood disorders, and as a Medical Advisor, you will be at the heart of this mission. Our inclusive work culture fosters collaboration and innovation, providing ample opportunities for professional growth while ensuring that your contributions directly enhance patient outcomes. With a commitment to long-term health and a legacy of excellence, joining us means becoming part of a team that values diverse perspectives and strives for extraordinary results.
