Description
This role is an ideal stepping-stone for a Clinical Research Associate, offering training and development to plan and progress your career. You'll have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.
As a Clinical Research Associate, you'll work on global projects with a regional or home state travel remit, using cutting-edge in-house technology. Your typical responsibilities might include:
- 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'll need to be comfortable collaborating and communicating with a variety of colleagues and customers, and have a good basic knowledge of applicable clinical research regulatory requirements.
Requirements:
- Bachelor's degree in a health care or other scientific discipline or educational equivalent
- At least 2 years of remote monitoring experience or as Study Coordinator
- Advanced in English
- Travel availability (50%)
If you want to make an impact in the global research market, where IQVIA is working to make a real difference in patient health, apply now and join their team.