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Labcorp Study Start-Up Specialist, sponsor-dedicated - 100% Home based in Maidenhead, United Kingdom

Labcorp Drug Development has supported the pharmaceutical industry in developing more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!

If you are looking to take on responsibility and leverage your know-how in the start-up phase of clinical trials - ensuring a successful start of important clinical studies in the UK -, this is the perfect opportunity. You will be working alongside our dedicated and supportive team of SSU experts and exclusively for one of our renowned international sponsors - in a role that allows you to have a real impact on people’s health and lives.

What we have to offer: a strong international support network, flexible working solutions that facilitate a genuine work-life balance, a highly competitive compensation package and the opportunity to significantly raise your profile in the industry.

This role is to focus on Initial and Amendment submissions, there is no site contract negotiations currently required. Candidates must have IRAS experience, preferably using the UK Combined Review/CWOW system, although the latter is not absolutely essential.

It's a fully Home based position, Independent management of own applications with support from close knit team. High expectation and emphasis on Quality and experience in QC’ing other team applications also required.

Candidates with experience of UK & ROI Ethics start up submissions. Oncology applications advantageous alongside any experience performing Competent Authority submissions in the UK & ROI (MHRA & HPRA). Knowledge of EUCTR application process desirable but not essential. Currently the team is contracted to making submissions for 1 Client/Sponsor.


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