Senior CRA II CFSP — Global Trials, Flexible Schedule

IQVIA; Madrid; Presencial; EUR 32.000 - 42.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

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Benefits package

Descripción de la vacante

IQVIA Spain is seeking a motivated Clinical Research Associate (CRA) to join our sponsor-dedicated team. You will perform site selection, initiation, monitoring and close-out visits across multiple therapeutic areas, while supporting patient recruitment planning.

The role offers exposure to regulatory requirements (GCP/ICH), data management collaboration with sites and client representatives, and the opportunity to grow within a global, reputable company.

Formación

• University degree in a scientific discipline or health care.
• Experience in Pharma Industry or Clinical Trials environment.
• Excellent command of Spanish and English language.
• 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.

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 per GCP and ICH guidelines.
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolutions.
• Collaborating with experts at study sites and with client representatives.

Conocimientos

Spanish & English fluency

Organizational skills

Time management

Interpersonal skills

Travel willingness

Driver's license B

Educación

University degree in scientific discipline or health care

Descripción del empleo

IQVIA Spain is seeking a motivated Clinical Research Associate (CRA) to join our sponsor-dedicated team. You will perform site selection, initiation, monitoring and close-out visits across multiple therapeutic areas, while supporting patient recruitment planning.

The role offers exposure to regulatory requirements (GCP/ICH), data management collaboration with sites and client representatives, and the opportunity to grow within a global, reputable company.