Precision for Medicine is seeking a Regulatory and Start Up Specialist in the UK to manage regulatory submissions and site activation activities. The role involves preparing submission dossiers, coordinating with authorities, ethics committees and project teams, and supporting budget/contract negotiations with sites.
Ideal candidates have at least 2 years in regulatory/start-up roles, a life sciences degree (RN or PharmD preferred), and strong English communication skills.
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UK Regulatory & Start-Up Specialist – Site Contracts employer: Precision for Medicine
At Precision Medicine Group, we pride ourselves on fostering a dynamic and inclusive work culture that empowers our employees to thrive. As a Principal Innovation Business Analyst, you will enjoy the flexibility of remote work from the UK while collaborating with cross-functional teams to drive meaningful change in healthcare through innovative AI solutions. We are committed to your professional growth, offering continuous learning opportunities and a supportive environment where your contributions directly impact our mission to improve patient outcomes.
