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 (f/m/d), 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 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 Site Management department, we support pharma clients of different size with conducting clinical trials in different projects. Within this team, you will focus on a comprehensive clinical trial management in a variety of indications and learn about the diverse scientific approach of the sponsors. Beside establishing strong relationships with the global study team 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.

Applicants should have:

• A Bachelor's or higher-level degree in a health care or other scientific discipline or educational equivalent
• As a CRA at least one one year of on-site monitoring experience, as a SrCRA at least three years 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
• Flexibility to travel up to 60% of the working time

In return we offer:

• Interesting projects and a variety of indications
• Working with high-level equipment and technical solutions
• A competitive benefits package: home-office, company car, accident insurance and more

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

Please apply with your English CV, motivation letter and your certificates and reference letters.

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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.