Tipo de jornada
Sin especificar
Tipo de contrato
Sin especificar
Salario
35.000€ - 50.000€ bruto/año
Estudios mínimos
Sin especificar
Descripción del empleo
- Be responsible for the successful conduct of clinical trials
- International Company with Career Progression
International CRO Company especialized in Clinical Trials and Consulting, present in America, Europe and Asia.
- Conduct qualification, initiation, monitoring and close the visits.
- Provide ongoing updates and support to project management
- Ensure clinical data integrity and meet study timelines.
- Assist with regulatory and study start-up activities including contract and budget negotiations.
- Attend global project meetings including investigator meetings and global team teleconferences.
- Complete assigned training programs in drug development processes, therapeutic areas, Good Clinical Practices (GCPs) and any applicable local regulatory requirements.
- May serve as mentor / trainer for CRAs; may include conducting training/assessment visits.
- May function in the role of Lead CRA for assigned project(s).
- Permanent and Full time (40h/week) position.
- Conditions according to candidate experience.
- Meal card: allowance of 11€/worked day.
- Medical Insurance for the employee and family.
- Life Insurance.
- 25 vacation days + n.º of days stipulated on the CBA.
- Possibility of Car allowance.
Requisitos mínimos
- Life science Degree. Monitoring MSc will be a plus.
- At least 3 years of clinical research experience as a CRA or related role.
- Excellent knowledge: ICH-GCP and regulatory.
- Fluent in Local Language and English (both oral and written).
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