CRA I - Santiago, Chile | IQVIA Job

Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. 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’ll 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’ll 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 2 years of remote monitoring experience or as Study Coordinator.
-Advanced in English.

-Travel availability (50%)
-Alternatively, you should have an equivalent combination of education, training and experience