Novo Nordisk in the United Kingdom seeks a Start Up Specialist to deliver regulatory, ethics and national approvals for clinical trials. You will work with the CDC UK team to negotiate site contracts, secure approvals, and activate sites in line with UK regulations and ICH GCP.
Key responsibilities include submission leadership via IRAS, preparing Clinical Trial Agreements (mCTA), and coordinating amendments with Trial Managers while ensuring timely delivery and compliance with Novo Nordisk SOPs.
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Launch-Ready UK Clinical Trial Start-Up Specialist in Crawley Down 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.
