20 publicaciones de empleo destacadas en quality program associate (¡Están contratando!)

Clinical Research Associate II - Portuguese speakers
Parexel —Madrid, Madrid provincia
- Microsoft Word
- Español
- Microsoft Excel
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- Teletrabajo
- Inglés
- Máster
- Grado
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Veeva Systems —En remoto
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- DevOps
- Inglés
- Oficina
- Teletrabajo opcional
- Abono gimnasio
Associate Director - T&D Overhead Transmission Lines
AECOM —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Grado
- Construcción
- Ingeniería eléctrica
- Seguro dental
- Vacaciones pagadas
Software Implementation Consultant, Proficient in English and German
Avature —Málaga, Málaga provincia
- Jornada completa
- Inglés
- Máster
Data Consultant - OpenData Europe
Veeva Systems —En remoto
- Jornada completa
- Teletrabajo
- CRM software
- Informática
- Inglés
- Teletrabajo opcional
- Seguro de vida
Customer Care Representative (6 months)
BD —San Agustín de Guadalix, Madrid provincia
- Microsoft Excel
- Salesforce
- Inglés
3d
R&D Thermodinamical Engineer
Bosch-HomeComfort —Vacarisses, Barcelona provincia
- Jornada completa
- Sistemas ERP
- Inglés
- Grado
Solicitud rápida
4d
Associate Account Manager
Amazon EU SARL (Spain Branch) - C16 —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Español
- Microsoft Excel
23h
Sales Excellence CoE Application Architecture Associate Manager
Accenture —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Microsoft Excel
- Ventas
- Inglés
SAP SuccessFactors Senior Consultant (EC, Time)
SD Worx —Málaga, Málaga provincia
- Inglés
- Oficina
- Recursos humanos
Solicitud rápida
12d
Inventory Control & Quality Assurance Area Manager
Amazon Spain Fulfillment, S.L.U. —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Inglés
- Microsoft Office
Associate Director - Cables
AECOM —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Español
- Inglés
- Desarrollo de negocios
- Seguro dental
- Vacaciones pagadas
Structured Core Trade Associate
SCH Banco Santander, S.A. —Boadilla del Monte, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Español
- Microsoft Excel
- Abono gimnasio
- Seguro de vida
1d
M&A Associate (Infrastructure & Industrials) - SCIB
SCH Banco Santander, S.A. —Madrid, Madrid provincia
- Español
- Microsoft Excel
- Inglés
- Abono gimnasio
- Seguro de vida
AWS Architect
SoftwareONE —Madrid, Madrid provincia
- Trabajo híbrido
- Español
- Inglés
- AWS
5h
System Integration Specialist
Progenika Biopharma SA —Derio, Vizcaya provincia
- Jornada completa
- Trabajo híbrido
- Doctorado
- Inglés
- Investigación
Advanced Field Service Engineer
Beckman Coulter Life Sciences —Valencia, Valencia provincia
- Jornada completa
- Inglés
- Investigación
- Grado
- Seguro dental
- Vacaciones pagadas
13d
GIE Senior Packaging Engineer
BD —San Agustín de Guadalix, Madrid provincia
- Inglés
- Máster
- Grado

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Clinical Research Associate II - Portuguese speakers

Parexel -
Madrid, Madrid provincia

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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

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