Description
We are looking for a Clinical Research Associate (CRA) to join our team. As a CRA, you will have the opportunity to plan and progress your career in the direction you choose, with dedicated mentoring and structured quarterly reviews on performance, promotion and bonus awards.
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
To be successful in this role, 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 1.5 - 2 years of on-site monitoring experience
- Fluent in Greek language
- Good written and verbal communication skills including good command of English language
- Requires frequent travel to sites
- Flexible about location, but location must have good connectivity to travel
- Home-based