*Late Phase CRA (f/m/d) - office-based or home-based in Switzerland*

Apply nowLocations: St. Prex, Switzerland ; Basel, Switzerland Full timeR1140371Date Posted: 08.06.2020

Job description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

We are offering an exciting job opportunity as Late Phase CRA (f/m/d) to work mainly in the field of Late Phase / Non-Interventional Studies and to join our RWE Department office-based or home-based in Switzerland.  

As you develop your career as a CRA, this role is an ideal stepping-stone. It offers you a unique opportunity to expand your skills and experience in the realm of real-world and late phase research. You will also have training and development to plan and progress your career in the direction you choose. And you will not do it alone – you will have dedicated mentoring and receive structured quarterly reviews to enable your performance and success.

Award winning and innovative, we will 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 will be building a smart and flexible career with no limits.

While projects vary, your typical responsibilities might include: 

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation for Phase IV/NIS projects


• 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


• Taking part in the study start-up process - contracts management, EC, CA submissions 


• Covering Switzerland

You 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 and a good knowledge of applicable clinical research regulatory requirements.


• Alternatively, you should have an equivalent combination of education, training and experience 


• Fluent French, Italian and English language skills, German language skills would be a plus


• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint


• Excellent organizational and problem-solving skills


• Effective time management skills


• Ability to manage competing priorities

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. 

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Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

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