10 Biomedicina jobs in Praha, Česko.

IQVIA seeks a Clinical Research Associate to support biotech development projects in Prague. The role involves site monitoring, protocol adherence oversight, and data management across the clinical trial lifecycle, from early phases through closeout.

Clinical Research Associate Your responsibilities will include: - Performing site selection, initiation, monitoring and close-out visits - Supporting the development of a subject recruitment plan - Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical

Senior Clinical Research Associate position at a global contract research organization, overseeing clinical trial monitoring and site management in a sponsor-dedicated model.

Přijmeme biomedicínského inženýra pro Oddělení zdravotnické techniky. Nástup možný po dohodě.

Clinical Research Associate IQVIA Czech Republic is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA.

Clinical Research Associate role focused on site monitoring and management for biotech studies in Prague. Responsible for conducting monitoring visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across assigned study sites.

Overview The Learning Delivery Quality Lead is responsible for delivering onboarding, role-readiness, and capability development programs for Clinical Operations staff.

Job offer Alcedis is a well-established clinical research organization headquartered in Germany, with over 30 years of experience in managing clinical studies.

Senior CRA, home based, Czech Republic ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Senior Clinical Research Associate position at ICON involving clinical trial monitoring, site management, and data quality assurance. The role operates within a sponsor-dedicated model, requiring travel and independent responsibility for trial deliverables across multiple sites.