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

• 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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