Descripción de la oferta
IQVIA in Barcelona, Spain, seeks an experienced Regulatory Affairs professional to lead EU submissions and CTIS management, with at least 8 years in pharma/biotech. You will provide strategic regulatory advice and oversee CTIS lifecycle activities. The role requires independent work, strong stakeholder management, and mentoring junior staff, plus oversight of timelines, budgets, and client relations. Required: Bachelor's in Life Sciences; Master's preferred. #J-18808-Ljbffr
