Hybrid CRA II: Multisponsor (Madrid/Barcelona)

Syneos Health, Inc.; Madrid; Híbrido; EUR 42.000 - 62.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid work model

Descripción de la vacante

Syneos Health is seeking a CRA II for multisponsor studies in a HYBRID Madrid or Barcelona setting. You will perform site qualification, initiation, monitoring, and close-out visits, ensuring regulatory and GCP compliance. Responsibilities include informed consent verification, ISF/TMF reconciliation, data review, and issue resolution.

Travel up to 75% is required within a dynamic clinical environment. The role requires a bachelor’s degree or RN with relevant monitoring experience, strong

Formación

• Bachelor’s degree or RN or equivalent combination of education, training and experience.
• 1+ year of independent on-site monitoring.
• Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements.
• Good computer skills and ability to embrace new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75%.

Responsabilidades

• Performs site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote) ensuring regulatory and GCP compliance.
• Verifies informed consent processes and protects subject confidentiality.
• Reviews site data and documents; drives query resolution to closure within timelines.
• Manages IP inventory, labeling, and storage per protocol.
• Ensures ISF vs TMF alignment and archiving per guidelines.
• Supports recruitment, retention and tracking of study observations.

Conocimientos

Independent on-site monitoring

Excellent communication

Good computer skills

Adaptable to new technologies

Travel up to 75%

Educación

Bachelor’s degree or RN in a related field or equivalent

Descripción del empleo

Syneos Health is seeking a CRA II for multisponsor studies in a HYBRID Madrid or Barcelona setting. You will perform site qualification, initiation, monitoring, and close-out visits, ensuring regulatory and GCP compliance. Responsibilities include informed consent verification, ISF/TMF reconciliation, data review, and issue resolution.

Travel up to 75% is required within a dynamic clinical environment. The role requires a bachelor’s degree or RN with relevant monitoring experience, strong