Regulatory & Start-Up Specialist — Clinical Trials
Precision for Medicine in the UK is seeking a Regulatory and Start Up Specialist to join our growing team. You will deliver timely site activation readiness, manage regulatory submissions, and liaise with authorities to obtain approvals.
Ideal candidates have a life sciences degree, experience with regulatory submissions and contracts/budget negotiation, fluent English, and strong organizational and communication skills. This role offers exposure to global trials within a dynamic CRO environment.
As a UK Regulatory & Start-Up Specialist — Clinical Trials, you will play an important part at Precision Medicine Group in United Kingdom.
We have an opening for a UK Regulatory & Start-Up Specialist — Clinical Trials in United Kingdom within Legal, Management & Operations.
This role, UK Regulatory & Start-Up Specialist — Clinical Trials at Precision Medicine Group, could be your next opportunity.
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