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Beca de Ensayos Clínicos en Abbott

Convenio de Prácticas Madrid

Descripción:
Field Clinical Operations Specialist Internship
Start Date: July or August

Full time internship.
Location: Las Tablas (Madrid)

Lenght: 1 year

Responsibility: 1

• Oversee the progress of a project research, and ensure that it is conducted, recorded and reported in accordance with the protocol, standard operating procedures, GCP-ICHm and the applicable regulatory requirements.

Responsability 2
• Logistic and technical support to clinical department, mainly to Clinical Managers: collection of technical and clinical data on site and validation of data through quality control process
• Participation to study initiation under co-ordination of Clinical Managers: review and/or translation of clinical investigation plan and case report forms, choice of local investigators, submission to local authorities, ethical committees and hospital/clinic administrative services
• Follow-up of clinical studies on site according to clinical investigation plan designed by the Clinical Departments (Europe or US), including collection of clinical and technical data.
Field Clinical Operations Specialist Internship
Start Date: July or August

Full time internship.
Location: Las Tablas (Madrid)

Lenght: 1 year

Responsibility: 1

• Oversee the progress of a project research, and ensure that it is conducted, recorded and reported in accordance with the protocol, standard operating procedures, GCP-ICHm and the applicable regulatory requirements.

Responsability 2
• Logistic and technical support to clinical department, mainly to Clinical Managers: collection of technical and clinical data on site and validation of data through quality control process
• Participation to study initiation under co-ordination of Clinical Managers: review and/or translation of clinical investigation plan and case report forms, choice of local investigators, submission to local authorities, ethical committees and hospital/clinic administrative services
• Follow-up of clinical studies on site according to clinical investigation plan designed by the Clinical Departments (Europe or US), including collection of clinical and technical data.
Requisitos:

• Educational background: Bachelor Sciences, Registered Nurse, Lab technician. Master in Clinical Trials Monitoring or just having finalized the Master
• Soft Skills:
• Must be able to use discretion and handle sensitive/confidential information.
• Must have strong organizational skills and attentiveness to detail.
• Lenguage: The ability to read, write, and communicate effectively in English is also required; this requirement includes clear, understandable speech, demonstrated comprehension skills, and demonstrated competence in English spelling, grammar and punctuation.
• IT (Microsoft office, specific software etc.). Microsoft office
Informática: No indicado
Idiomas: Inglés alto 
localidad: Madrid, España
Jornada: Horario de Mañanas y tardes
Contrato: Convenio de Prácticas para estudiantes.
Remuneración: De 700 a 900 euros/mes
Más ofertas de: Abbott Laboratories
Buscar prácticas en: #ciencia #investigacion #madrid
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