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 flexible, supportive environment.
Compensaciones / Ventajas
- 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

📌 Clinical Research Associate 2 (Barcelona)
🏢 MindMatch
📍 Barcelona