Remote CRA II – Gastro/GU Trials Specialist (Spain)

Syneos Health, Inc.

Madrid

Híbrido

EUR 42.000 - 65.000

Jornada completa

hace 7 horas
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Generador de candidaturas

Transforma esta oferta en una entrevista — un currículum y una carta de presentación creados pensando en lo que quiere el empleador.

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Descripción de la vacante

Syneos Health is seeking a CRA II for Madrid with sponsor-dedicated oversight. This remote role in Spain requires experience in gastroenterology and genitourinary studies and involves site qualification, monitoring, and close-out activities across trials.

Join a global team committed to delivering lifesaving therapies. You will collaborate with investigators, manage data quality, and ensure adherence to ICH/GCP and local regulations while supporting delivery milestones.

Formación

  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
  • 2-5 years of experience as CRA or similar monitoring role.
  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
  • Must demonstrate good computer skills and be able to embrace new technologies.
  • Excellent communication, presentation and interpersonal skills.
  • Ability to travel up to 75% on a regular basis.

Responsabilidades

  • Performs site qualification, initiation, monitoring, and close-out visits (on-site or remote) per protocol.
  • Verifies informed consent and protects subject confidentiality.
  • Reviews ISF/TMF and ensures proper archiving per guidelines.
  • Manages IP inventory, labeling, storage, and distribution.
  • Ensures accurate CRF data and drives query resolutions.

Conocimientos

Excellent communication
Good computer skills
Interpersonal skills
Travel up to 75%

Educación

Bachelor’s degree or RN

Descripción del empleo

Syneos Health is seeking a CRA II for Madrid with sponsor-dedicated oversight. This remote role in Spain requires experience in gastroenterology and genitourinary studies and involves site qualification, monitoring, and close-out activities across trials.

Join a global team committed to delivering lifesaving therapies. You will collaborate with investigators, manage data quality, and ensure adherence to ICH/GCP and local regulations while supporting delivery milestones.

Consigue la evaluación confidencial y gratuita de tu currículum.

o arrastra y suelta tu archivo aquí

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