CRA2 - Argentina
Buenos Aires, Argentina
Full time
R
CRA 2 - Homebased
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 general 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.
- 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

REQUIREMENTS
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- At least 2 years of on-site monitoring experience (Mandatory)
- Advanced in English.
- Availability to travel (50% of time)
- Located in Buenos Aires, Argentina.
- Alternatively, you should have an equivalent combination of education, training and experience

EEO Minorities/Females/Protected Veterans/Disabled
Location
São Paulo, Brazil
Buenos Aires, Argentina
Bogota, Colombia
Full time
R
Job Overview
Direct and manage the delivery of all required site activation, maintenance and regulatory acti

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