Associate Cra

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 resolutionThe CRA training duration is 6 months (upon performance)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.- Advanced in English.- Availability to travel (70% of the time).- Based on Mexico City (hybrid role).- Successful completion of a CRA Trainee Program (highly valued but not mandatory).IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at