Descripción de la oferta
Experteer Overview
As a Junior CRA, you support a Sponsor-dedicated team to gain broad exposure across therapeutic areas while building a solid clinical research foundation. You will work closely with study sites and clients to drive quality data and regulatory compliance. The role focuses on site visits, recruitment planning, and progress tracking to ensure trials run smoothly. This is an opportunity to grow professionally in an international, reputable company with structured development programs.
Compensaciones / Beneficios
• Perform site selection, initiation, monitoring and close-out visits
• Support the development of a subject recruitment plan
• Evaluate site practices for quality and regulatory compliance (GCP and ICH)
• Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolutions
• Collaborate with study site experts and client representatives
Responsabilidades
• 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
• Strong organizational, time management and problem-solving skills
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Flexibility to travel
• Driver's license class B
Requisitos principales
• Mobile phone
• attractive benefits package
• flexible work schedules
