IQVIA is looking for a Quality Control expert in Barcelona. The role involves reviewing Medical Writing deliverables, ensuring accuracy and compliance. Candidates should have a Bachelor's, Master's, or Ph.D. in Life Sciences and at least 8 years of experience in clinical trial documentation. Responsibilities include training staff and maintaining high-quality standards. The position requires excellent communication skills and attention to detail. Join IQVIA's dynamic team and contribute to quality assurance in drug development.
#J-18808-Ljbffr