Clinical Trial Assistant (CTA) en PRA INTERNATIONAL ESPAÑA

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Celebramos 25 años


Clinical Trial Assistant (CTA)

Fecha de la oferta: 9 Ago.
Empresa que publica esta oferta: PRA INTERNATIONAL ESPAÑA
As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.

At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community.
Número de vacantes: 1
Provincia/s: Madrid

Descripción

Descripción: We are looking for a permanent CTA based in Madrid to work fully dedicated to one of our global pharmaceutical clients.

Operating within the scope of the Clinical Development Plan, ICH-GCP guidelines and in accordance with the study protocol, local and international regulatory requirements and company procedures, the Clinical Trial Assistant (CTA) works to support the completion and coordination of various logistical and administrative tasks.

The Clinical Trial Assistant’s (CTA) work is varied, fast-paced and quality focused. Typical duties will include supporting other members of the local study team, including Clinical Research Associates and Lead Monitors, collecting data required for regulatory submissions, document tracking (contracts, financial agreements, patient informed consent forms, insurance certificates) and managing the delivery of non-drug related study supplies. Maintaining constructive relationships with site staff (eg Investigators, Study Coordinators etc) as well as with colleagues within the organisation, the Clinical Trial Assistant is responsible for tracking site budget related matters, including processing invoices, tracking payments etc. The maintenance and updating of the Trial Master File also falls within the CTA’s remit.

The Clinical Trials Assistant may also be responsible for scheduling meetings, updating Excel trackers and coordinating the translation of site documentation.

We will positive consider candidates with 33% disability certificate
Edad máxima para el puesto: 65 años.
Tipo de contrato: Indefinido
Remuneración anual: According to the experience
Ventajas sociales o económicas: Private health insurance, lunch vouchers, flexible working hours. Salary according to the experience

Requisitos

Requisitos: To be considered for this position, you must have recent experience in the Clinical Research field as a Clinical Trial Assistant.

Fluency in English is essential, along with proficiency in the use of Microsoft Office suite.

Demonstrable experience of working to high quality standards and resolving issues will also feature in your profile. The ability to effectively communicate with others and foster positive working relationships will guarantee success within this role.
Nivel de estudios mínimo requerido: Diplomado
Experiencia profesional mínima requerida: 1 año
Disponibilidad para viajar requerida: Ninguna

Comparte esta oferta:

Esta oferta ha recibido 55 inscripciones.