*CRA or Senior CRA (m/w/d) - sponsor dedicated, office- or home-based in Austria*

IQVIA
Vienna
Montag, 21. Juni 2021
Mittwoch, 30. Juni 2021
R1213106
Vollzeit
Festanstellung
External Job Description

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. At IQVIA™ we do not believe in a ‘career ceiling.’ You can make the CRA/Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

In our Clinical Functional Service Partnership models, we work in a close partnership with key customers in order to deliver a comprehensive clinical trial management. Within this team, you will focus on different projects of one single 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
  • 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.

We believe in hiring the best clinical talent in the industry.

Applicants should have:

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • At least one year of on-site monitoring experience
  • Alternatively, you should have an equivalent combination of education, training and experience
  • Strong written and verbal communication skills including good command of German and English language

In return we offer a competitive benefits package: company car (after probation period of 1 month); Accident insurance and Meal vouchers (for office-based employees).

Monthly gross salary: starting at 3.000 EUR basic - an overpay is possible according to skills and working experience.

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

Due to the international scope of our business please apply with English version CV and your certificates and reference 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.