Cra2 - Homebased

**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 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
- 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**

You should have:

- 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_