Associate Cra - Buenos Aires, Argentina - IQVIA
Descripción
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.
While projects vary, your typical responsibilities might include:
- Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
- 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
The CRA training duration is 6 months.
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 (would be a plus if comes from Pharmacy, Biochemistry, Nutrition). - Advanced in
English. - Availability to
travel (50% of the time). - Based on Buenos Aires, this is an office based role.
- Successful completion of a CRA Trainee Program (highly valued but not mandatory).
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