¡No te pierdas nada!
Únete a la comunidad de wijobs y recibe por email las mejores ofertas de empleo
Nunca compartiremos tu email con nadie y no te vamos a enviar spam
Suscríbete AhoraTransporte y Logística
1.237Comercial y Ventas
1.154Informática e IT
954Adminstración y Secretariado
782Comercio y Venta al Detalle
533Ver más categorías
Ingeniería y Mecánica
521Desarrollo de Software
476Industria Manufacturera
443Educación y Formación
421Derecho y Legal
315Instalación y Mantenimiento
297Marketing y Negocio
274Diseño y Usabilidad
204Sanidad y Salud
161Arte, Moda y Diseño
137Publicidad y Comunicación
118Hostelería
109Construcción
108Contabilidad y Finanzas
108Artes y Oficios
102Recursos Humanos
96Alimentación
76Atención al cliente
66Turismo y Entretenimiento
52Producto
45Banca
42Inmobiliaria
42Seguridad
32Cuidados y Servicios Personales
25Farmacéutica
24Energía y Minería
15Social y Voluntariado
12Deporte y Entrenamiento
4Seguros
4Telecomunicaciones
2Agricultura
1Editorial y Medios
1Ciencia e Investigación
0Parexel
Madrid, ES
Clinical Research Associate I
Parexel · Madrid, ES
. Excel LESS Word
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.
We are currently looking for a Clinical Research Associate I to join our Clinical Operations Team in Spain.
This role can be office-based in Madrid or decentralized in the region of Madrid.
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.
On your first day we’ll expect you to have:
- Experience in clinical research e.g. as a Clinical Research Coordinator, with understanding of clinical trials methodology and terminology.
- 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 knowledge of the Spanish and English languages is required.
- 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.