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.
Número de vacantes: 1
Modalidad de trabajo: Full remoto (100%)




Tipo de contrato: Full time.
Remuneración anual: *****€ nett/month
**Ventajas sociales o económicas**
Annual bonus, depending on objectives.
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**Requisitos**
- 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.
**Áreas terapéuticas**
**Oncología**
**Habilidades**
**Ordenada y organizada**
**Capacidad multitarea**
**habilidades de comunicación y relación interpersonales**
Estudios mínimos
Diplomado en Ciencias de la Salud
**Idiomas**:
Inglés nível Alto.
Experiência mínima
1 año
Disponibilidad para viajar
El 60% del tiempo laboral

📌 Clinical Research Associate (Cra) (Colima)
🏢 Importante empresa
📍 Colima