3 publicaciones de empleo destacadas de clinical associate en spain (¡Están contratando!)

Clinical Research Associate II - Portuguese speakers
Parexel —Madrid, Madrid provincia
- Microsoft Word
- Español
- Microsoft Excel
Associate Principal, Business Analyst
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Oficina
- Project management
7h
Associate Feasibility Strategist- Remote
Thermo Fisher Scientific —España
- Jornada completa
- Teletrabajo
- Microsoft Powerpoint
- Microsoft Excel
- Informática

More jobs to discover

Find similar jobs that you might be interested in.

Associate Principal, Business Analyst
AstraZeneca —Barcelona, Barcelona provincia
There are many things I enjoy when working at AstraZeneca, mainly the Speak up culture, the great colleagues that are in my teams, the great products that…
7h
plaça de SAP Business One Developer / Analyst - Mid-Level CIDO
Barcelona Supercomputing Center-Centro Nacional de Supercomputación (BSC-CNS) —Barcelona, Barcelona provincia
Barcelona Supercomputing Center-Centro Nacional de Supercomputación (BSC-CNS). 1 plaça de SAP Business One Developer / Analyst - Mid-Level. Concurs o…

Quiero recibir la alerta de empleo más reciente de clinical associate en spain

Al iniciar sesión en tu cuenta, aceptas las Condiciones del servicio de SimplyHired, nuestra Política sobre cookies y nuestra Política de privacidad.

Clinical Research Associate II - Portuguese speakers

Parexel -
Madrid, Madrid provincia

Solicitar ahora

Detalles del empleo

Cualificaciones

Microsoft Word
Español
Microsoft Excel
Investigación clínica
Inglés
Investigación
Grado
Farmacia
Portugués

Descripción completa del empleo

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values, Patients First, Quality, Respect, Empowerment & Accountability.

This role is based in the regions of Madrid or Barcelona.

Your time here

At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through to close-out.

As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.

What you’ll do

Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

More about you

On your first day we’ll expect you to have:

Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
Ability to perform all clinical monitoring activities independently.
Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.
Strong interpersonal, written, and verbal communication skills within a matrixed team.
Fluent command of Spanish, Portuguese and English (written and oral).
Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
A client-focused approach to work and flexible attitude with respect to assignments/new learning.
The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
An honest and ethical work approach to promote the development of life changing treatments for patients.
Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.

If you are ready to join Parexel’s Journey, please apply!

Solicitar ahora

Refina tu búsqueda

clinical associate empleos en spain

Clinical Research Associate II - Portuguese speakers

Associate Principal, Business Analyst

Associate Feasibility Strategist- Remote

More jobs to discover

Quiero recibir la alerta de empleo más reciente de clinical associate en spain

Related Searches

Herramientas para candidatos

Herramientas para empresas

Buscar

Mantener la conexión