TRABAJO REGULATORY AFFAIRS STUDY START BARCELONA, BARCELONA

Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence providing guidance and support to study teams...

You will work closely with study implementation teams, as well as clinical operations, data management and regulatory affairs to ensure the solutions meet the requirements...

Excellent understanding of clinical study management including monitoring, study drug handling and data management... supporting/participating in regular qc checks...

Prepare and present findings from real-world evidence studies to internal and external stakeholders, including scientific conferences, ministries of health, regulatory...

Global market development project manager - rhinology & gastroenterology - vie contract   location: barcelona, spain target start date:     imove, the sanofi...