Clinical Research Associate I / II en Parexel

Clinical Research Associate I / II
Find Your Path
There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey, go further, and faster every time. What if you had a partner to support you to go to the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner that’s dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?
That’s Parexel. We’re a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we
Barcelona, Madrid, 21 Jul.
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 - but not limited to...
Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) & termination visits (TV) at assigned clinical sites & 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

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Numero de vacantes: 1
Tipo de contrato: Full Time
Remuneración anual: Competitive

Ventajas sociales o económicas
CRA Incentive Bonus Plan
Flexible Working Policy
Flexible Timetable
25 days of annual leave + Bank Holidays
Private Medical Insurance
Life Assurance
iPhones for traveling CRAs
Working Spain / Portugal

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On your first day we’ll expect you to have:
Previous relevant work experience (preferred).
Ability to perform clinical monitoring activities under supervision from the COL/LM.
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.
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.

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Estudios mínimos
Euskera nivel Nativo.
Inglés nivel Perfecto.
Experiencia mínima
1 año
Disponibilidad para viajar
El 40% del tiempo laboral

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