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

Location: Vienna, Austria
R1213106

When you join IQVIA as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development.

With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

  • Full Time
  • Level: Entry-level, Mid-level, Senior-level
  • Travel: Yes

Success profile

What makes sponsor-dedicated CRAs at IQVIA successful? Check out the top traits we’re looking for and see if you have the right mix.

  • COLLABORATIVE
  • DETAIL-ORIENTED
  • COMMUNICATOR
  • INDEPENDENT
  • CURIOUS
  • PROBLEM-SOLVER

Explore this
career path

As you grow your CRA career at IQVIA, you’ll play an important role in helping our customers drive healthcare forward and impact the lives of patients around the world.

Quote

Alberto

IQVIA offers a robust development plan for CRAs, including trainings, mentorship programs, and cross-functional career meetings. These conditions made me feel ready, confident and well-trained to execute the role of a CRA with quality and integrity.

Alberto, Clinical Research Associate 2
Oliver

IQVIA places real emphasis on the training and development of employees. This is invaluable for someone starting out or looking to progress their career in clinical research. I find it extremely rewarding to work for a company that strives to grow and retain its talent and equips you with the skills and experience needed to succeed in your career.

Oliver, Clinical Research Associate 1

What you
can expect

  • Professional Development

    Resources that promote your career growth

  • Work-Life Balance

    Leaders that support flexible work schedules

  • Growth Potential

    Clear pathways to success

  • Collaboration

    Teams that work together to achieve common goals

  • Variety

    Dynamic work environments that expose you to new experiences

  • Best-in-class Training

    Programs to help you build knowledge and gain skills

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

Apply now
Location: R1213106

Job description

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.

Apply now
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