Description
Join IQVIA today and make an impact on patients' outcomes as a Clinical Research Associate.
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Responsibilities
- 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
Qualifications
- Minimum of a Bachelor's Degree in a scientific discipline or healthcare
- Experience of 1 year in on-site monitoring clinical trials
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable)
- Written and verbal communication skills including good command of Polish and English language
- Ability to establish and maintain effective working relationships with co-workers, managers, and clients
The potential base pay range for this role, when annualized, is 132,800.00 zł - 280,000.00 zł.