5,0
2 de fev. de 2026
Ex-funcionário(a), mais de um ano
Barcelona
Recomenda
Visão de mercado da empresa
Prós
Valuable hands-on experience in clinical research and clinical trials with a direct impact on patient care and drug development. Close collaboration with investigators, patients, sponsors, and monitors, helping to develop strong communication and organizational skills. Opportunity to gain in-depth knowledge of study protocols, GCP, regulatory requirements, and clinical data management. Dynamic role with exposure to multiple studies and therapeutic areas. Good foundation for career growth within clinical research.
Contras
High administrative and documentation workload requiring strong attention to detail. Can be stressful due to tight timelines, monitoring visits, audits, and regulatory inspections.