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CRA or Senior CRA, sponsor dedicated, home based - 5K SIGN ON

Aplica ya
Mapa de ubicación: Zaventem, Brussels-Capital Region, Belgium Full time R1249362

Descripción del trabajo

Create possibilities, even where it seems none exist. See every challenge as an opportunity. Discover new paths to success as you share stories of unparalleled data, transformative technology, advanced analytics and domain expertise coming together to advance human health. 

Join IQVIA™ as a CRA or Senior CRA, and you will have the opportunity to plan and progress your career in the direction you choose. In our Clinical Functional Service Partnership models, we work in a close partnership with key customers to deliver a comprehensive clinical trial management. Within this team, you will focus on different projects of one pharma client and gain direct and in-depth experience of collaborating with this sponsor.

Beside establishing strong relationships with the client and the involved investigators, you will conduct monitoring on complex clinical trials and assure the adherence to good clinical practices, standard operating procedures, and study protocols.

Responsibilities include:

  • 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
  • Collaborating and communicating with a variety of colleagues, the customer, and research site staff

Applicants should have:

  • A Masters’ or higher-level degree in a health care or other scientific discipline
  • At least one year of on-site monitoring experience, preferable with oncology trials
  • Good knowledge of applicable clinical research regulatory requirements and guidelines
  • Strong written and verbal communication skills in Dutch, French and English
  • Excellent organizational and problem-solving skills
  • Effective time management skills and ability to manage competing priorities
  • Ability to establish and maintain effective working relationships
  • Flexibility to travel and driving license class B

In return we offer:

  • Interesting projects and a variety of indications
  • Working with high-level equipment and technical solutions
  • A competitive salary and benefits package
  • Development opportunities, dedicated mentoring and receive structured reviews on performance, promotion and bonus awards.

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team

Please apply with your English CV and motivation letter as well as with your certificates and recommendation letters.

#CRASDAJD

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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