Clinical Start-Up Lead: Regulatory & Site Activation

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7lbz03

pFortrea is seeking a Site Start-Up Specialist to coordinate site start-up activities, manage essential documents, and ensure timely regulatory submissions.
You will work with the FSPx team and collaborate with sponsor sites to advance clinical trials.
/ppIdeal candidates have 2+ years in clinical research or regulatory submissions, strong organizational skills, and proficiency in Microsoft Office.
The role may involve both tempo parziale and full-time schedules with competitive compensation.
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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7lbz03