Buenos Aires, ArgentinaFull timeRWhether 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 adaptable career with no limits.While projects vary, your typical responsibilities might include:Performing site selection, initiation, monitoring and close-out visits,



plus maintaining appropriate documentationSupporting the development of a subject recruitment planEstablishing regular lines of communication plus administering protocol and related study training to assigned sitesEvaluating the quality and integrity of site practices - escalating quality issues as appropriateManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionYou 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 equivalentAt 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 experienceEEO Minorities/Females/Protected Veterans/Disabled
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📌 Delivery Lead, Human Data Projects | Remote (Córdoba)
🏢 Anyone AI
📍 Córdoba