Clinical Research Associate (CRA) GEIS-Grupo Español de Investigación en Sarcomas calendar_mont[...]

PMFarma; Las Palmas de Gran Canaria; A distancia; EUR 25.000 - 35.000; Jornada completa

Descripción de la vacante

A leading company in clinical development is seeking a Clinical Research Associate to monitor clinical trial sites primarily remotely. The role involves ensuring compliance with protocols, mentoring other CRAs, and maintaining the integrity of clinical data. Candidates should have a Bachelor’s in Science and at least one year of relevant experience, preferably in Oncology, along with strong communication skills.

Formación

• 1 year of clinical monitoring experience (preferably in Oncology).
• Strong communication and interpersonal skills.

Responsabilidades

• Perform site visits and monitor clinical activities.
• Mentor CRAs and collaborate on procedures.
• Review and verify clinical data for accuracy.
• Identify protocol deviations and risks.

Conocimientos

Communication

Interpersonal Skills

Presentation Skills

Fluency in English

Educación

Bachelor's degree in Science or equivalent

Descripción del empleo

• Perform site visits and monitor activities in accordance with protocol, GCP / ICH Guidelines, and applicable regulatory requirements, from SIV to SCV (phase I-IV)
• Mentor CRAs on monitoring, collaborate on procedures development, and query resolution.
• Review and verify case report forms and other clinical data for completeness and accuracy.
• Generate queries and manage resolutions with site staff.
• Maintain project tracking systems as required.
• Use expertise to identify and resolve complex site issues and deficiencies in documentation, communication, and the need for additional training.
• Identify protocol deviations or major risks to data integrity.
• Provide recommendations regarding site-specific actions.
• Act as a liaison between the company and study site personnel and be able to respond to site concerns and questions.
• IMP supply and control.
• Remote work will be approximately 90% of the time.
• Perform site visits and monitor activities in accordance with protocol, GCP / ICH Guidelines, and applicable regulatory requirements, from SIV to SCV (phase I-IV)
• Mentor CRAs on monitoring, collaborate on procedures development, and query resolution.
• Review and verify case report forms and other clinical data for completeness and accuracy.
• Generate queries and manage resolutions with site staff.
• Maintain project tracking systems as required.
• Use expertise to identify and resolve complex site issues and deficiencies in documentation, communication, and the need for additional training.
• Identify protocol deviations or major risks to data integrity.
• Provide recommendations regarding site-specific actions.
• Act as a liaison between the company and study site personnel and be able to respond to site concerns and questions.
• IMP supply and control.
• Remote work will be approximately 90% of the time.
• Bachelor's degree in Science or equivalent combination of education, training and experience.
• Prior 1 year of clinical monitoring experience (preferably in Oncology).
• Fluency in English.
• Excellent communication, presentation, interpersonal skills, both written and spoken.

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