CRA II - Multi-Sponsor Clinical Trials (Spain)

IQVIA; Madrid; Presencial; EUR 52.000 - 72.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

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Attractive benefits package

Descripción de la vacante

IQVIA Spain is seeking a Clinical Research Associate to join our sponsor-dedicated team in Madrid. The role focuses on site selection, initiation, monitoring, close-out visits, and supporting recruitment plans within a wide range of therapeutic areas.

You will ensure regulatory compliance and data integrity, coordinate with study sites and client representatives, and travel as required. Fluency in Spanish and English and a university health-care related degree are expected.

Formación

• University degree in scientific discipline or health care.
• Experience in Pharma Industry or Clinical Trials.
• Very good computer skills including MS Office.
• Excellent command of Spanish and English.
• Organizational, time management and problem-solving skills.
• Ability to travel and travel flexibility.
• Driver’s license class B.

Responsabilidades

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements.
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions.
• Collaborating with experts at study sites and with client representatives.

Conocimientos

Organizational skills

Problem-solving

Educación

University degree in scientific discipline or health care

Experience in Pharma Industry or Clinical Trials

Herramientas

MS Office

Driver's license (B)

Descripción del empleo

IQVIA Spain is seeking a Clinical Research Associate to join our sponsor-dedicated team in Madrid. The role focuses on site selection, initiation, monitoring, close-out visits, and supporting recruitment plans within a wide range of therapeutic areas.

You will ensure regulatory compliance and data integrity, coordinate with study sites and client representatives, and travel as required. Fluency in Spanish and English and a university health-care related degree are expected.