Associate Cra

hace 2 semanas

Buenos Aires, Argentina IQVIA A tiempo completo

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
- 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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