Clinical Research Associate (CRA) en PRA INTERNATIONAL ESPAÑA

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Clinical Research Associate (CRA)

Fecha de la oferta: 15 Abr.
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 15,000 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 CRA based in Madrid.

As a Clinical Research Associate, you will be dedicated to a company that values performance, recognises merit and has a high focus on quality. This environment encourages innovation, individuality and embraces people that want to be a part of it.

Key responsibilities include:

- Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.
- Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.
- Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
- Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.
- Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines


We believe our Clinical Operations team is second to none. You will receive the support you need to develop personally and professionally and work in an environment where you matter. Our team pushes forward together. United in solving problems, developing close site relationships and reaching the end goal. Operating as a key part of a global study team, the CRA plays a fundamental role in our clients’ drug development processes.
Tipo de contrato: Indefinido
Remuneración anual: According to experience
Ventajas sociales o económicas: SANITAS cover, lunch vouchers, permanent contract, flexible working hours.


Requisitos

Requisitos: You are:

Dedicated, collaborative and inspire others.

Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

- Independent experience as a CRA working in site management, including conducting monitoring visits for interventional trials, from either a pharmaceutical company or a CRO environment.
- A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
- You will be educated to degree level, have equivalent experience or be a licensed healthcare professional.
- Fluency in English is an absolute requirement.
- Experience in oncology trials will be an asset.
Nivel de estudios mínimo requerido: Diplomado
Idiomas requeridos: Inglés nivel Medio.
Experiencia profesional mínima requerida: 1 año
Disponibilidad para viajar requerida: El 20% del tiempo laboral

Comparte esta oferta:

Esta oferta ha recibido 93 inscripciones.