Clinical Research Associate
3 tygodni temu
IQVIA is seeking a Clinical Research Associate
As a Clinical Research Associate at IQVIA, you will be responsible for performing 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.
Key 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
Requirements:
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- Experience in on-site monitoring of clinical trials
- Alternatively, you should have an equivalent combination of education, training and experience
- Written and verbal communication skills including good command of Polish and English language
About IQVIA:
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.
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