Klinischer Monitor / CRA or Senior CRA

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Discipline
Clinical Research
,
Clinical Research Associate
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
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Job Details
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Job Details

UIQVIA™ 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.

 
As you develop your career as a
CRA or Senior CRA
, this role offers you 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.

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
• 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.

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

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

German

language skills and a good level of

English

• Less experienced candidates are supposed to work in one of our offices in Neu-Isenburg, Freiburg/Br. or München-Sauerlach. Experienced employees are welcome to work home-based, offering you total flexibility to manage your own time. However, you must be willing to travel 60% of the time, and must have a suitable location from which to work in your home (if applicable).

 
Join Us
 
 
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.

 
 
Forge a career with greater purpose, make an impact, and never stop learning.
 

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