IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a...
IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
As an experienced
Clinical Research Associate, you could be looking to broaden your therapeutic or geographic exposure, or perhaps considering your future within our vast selection of possibilities to take your next career steps. At IQVIA, you’ll have training and development to plan and progress your career in the direction you choose; 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. All the while, receiving structured quarterly reviews on performance, promotion and bonus awards.
And with our award-winning, cutting-edge technology, you will work on global projects on a variety of therapeutic areas in phases I-III. You’ll be building a smart and flexible career with no limits.
*The successful individual can work either from our Madrid or Barcelona office or remotely from home (different locations of Spain)*
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
+4 years of on-site monitoring experience
Full proficiency of Spanish and English
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
We know that meaningful results require not only the right approach but also the right people
. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.
Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™.
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