Description
We are seeking an experienced Clinical Research Associate (CRA) to join our team in Belgrade, Serbia. As a CRA, you will be responsible for performing site selection, initiation, monitoring and close-out visits, as well as maintaining appropriate documentation.
Your typical CRA responsibilities will 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 should have:
- A Bachelor's degree in a healthcare field, MD or Pharmacist preferred
- At least 1 year of on-site monitoring experience
- Good written and verbal communication skills, including fluent command of English and Serbian language
- A valid driver's license, as the role requires frequent travel to sites
- Ability to collaborate and communicate with a variety of colleagues and customers, with good knowledge of applicable clinical research regulatory requirements
IQVIA creates intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.