Overview In this role you work within IQVIAs sponsor-dedicated team to support clinical trial operations across multiple therapeutic areas. You will conduct site visits, help develop recruitment plans, and ensure site practices meet GCP/ICH standards. You will track regulatory submissions, recruitment, CRF completion, and data queries while collaborating with study sites and client representatives. This position offers growth opportunities within a global, reputable company and a versátil, supportive environment.
Compensaciones / Beneficios Resources that promote your career growth
Leaders that support flexible work schedules
Mobile phone
Attractive benefits package
International, reputable company
Stable, supportive environment
Responsabilidades Perform site selection, initiation, monitoring and close-out visits
Support development of a subject recruitment plan
Evaluate site practices for regulatory compliance (GCP/ICH)




Track progress on regulatory submissions, recruitment, CRF completion, and data queries
Collaborate with study sites and client representatives
Requisitos principales University degree in scientific discipline or health care
Experience in Pharma Industry and/or Clinical Trials environment
Very good computer skills including MS Office
Excellent command of Spanish and English
Organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships
Flexibility to travel
Driver's license class B
organizational skills
time management
problem-solving
Good Clinical Practice (GCP) and ICH guidelines
regulatory submissions tracking
MS Office

📌 Junior Clinical Research Associate (Barcelona)
🏢 MindMatch
📍 Barcelona