CRA1

IQVIA LLC

Buenos Aires

Sur place

ARS 45 609 000 - 68 414 000

Plein temps

14 jours+
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Résumé du poste

IQVIA LLC is looking for a Clinical Research Associate (CRA) to advance your career with training and mentoring, enabling progression through performance reviews and bonuses. This role supports global projects with regional travel, offering a structured path and access to in-house technology.

You will collaborate with colleagues and customers, with a focus on regulatory requirements and site management. The position emphasizes a smart, flexible career trajectory with opportunities for promotion.

Qualifications

  • Bachelor's degree in a health care or other scientific discipline or educational equivalent.
  • At least 2 years of remote monitoring experience or as Study Coordinator.
  • Advanced in English.
  • Travel availability (50%).

Responsabilités

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining documentation.
  • Supporting the development of a subject recruitment plan.
  • Establishing regular lines of communication and administering protocol and study training to assigned sites.
  • Evaluating the quality and integrity of site practices and escalating quality issues as appropriate.
  • Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.

Connaissances

Advanced English
Remote monitoring experience
Communication skills

Formation

Bachelor's degree in health care or scientific discipline

Description du poste

Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we’ll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You’ll be building a smart and flexible career with no limits.

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

Typical responsibilities
  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Qualifications
  • -A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • -At least 2 years of remote monitoring experience or as Study Coordinator.
  • -Advanced in English.
  • -Travel availability (50%)
  • -Alternatively, you should have an equivalent combination of education, training and experience

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.

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