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Clinical Study Manager
1 tydzień temu
Clinical Research Associate - IQVIA Biotech Poland
IQVIA Biotech seeks experienced professionals to manage clinical trials.
Join us at IQVIA and make a difference in patients' lives.
Job Overview
The Clinical Research Associate will be responsible for performing monitoring and site management tasks to ensure compliance with study protocols, regulations, and sponsor requirements.
Key Responsibilities
- Selecting and managing clinical trial sites, with a focus on high-quality documentation.
- Developing and implementing subject recruitment strategies in collaboration with the development team.
- Maintaining effective communication with assigned sites and delivering protocol and study-related training.
- Ensuring the quality and integrity of site practices and addressing any quality issues promptly.
- Tracking and resolving issues related to regulatory submissions, recruitment, case report forms, and data queries.
Requirements
- A degree in a healthcare or scientific field or equivalent education.
- At least 2 years of experience in on-site clinical trial monitoring, preferably in CVRM/Oncology.
- Strong written and verbal communication skills, including proficiency in Polish and English languages.