Regulatory and Start Up Specialist
Precision Medicine Group Is this your company? Claim it · Remote (UK) · Full-time
Description
Precision for Medicine is a global Clinical Research Organization with uniquely integrated offering which enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas. Due to our continued growth we are seeking a Regulatory and Start Up Specialist based in the UK to join our growing team. Apart from the experience with regulatory submissions, candidates will ideally also have contracts and budgets negotiation experience for the UK. Essential functions of the job include but are not limited to: Responsible for delivery, in terms of timeliness and quality, of site activation readiness within the assigned country/sites and foreseeing and mitigating any risks. Preparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission to Competent Authorities, Ethics Committees, and other applicable local bodies according to local requirements and within required timelines t…
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Questions about this job
Where is this Regulatory and Start Up Specialist job located?
It is listed as Remote (UK), so it can be done from home.
Who is hiring?
The employer shown on the listing is Precision Medicine Group.
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Is it full-time or part-time?
The listing type is Full-time.
When was this job posted?
It was posted on 11 November 2026. Jobs that stay open too long are closed automatically, so apply soon if you are interested.
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