The Clinical Research Associate II position involves performing monitoring visit activities to ensure compliance and adequacy at investigational sites, contributing to clinical studies primarily in oncology and rare diseases.
Ergomed is a specialized mid-size pharmacovigilance service provider, established in 2008, and is part of the Ergomed group. With a commitment to global organic growth, Ergomed has built a strong presence across Europe, North America, and Asia, offering services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance. The company prides itself on maintaining long-lasting relationships with pharmaceutical and biotechnology partners, covering all therapy areas, including medical devices. Ergomed values its employees by investing in their training and development, promoting well-being and mental health, and fostering a healthy work-life balance to ensure high-quality client service.
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Jobs from Ergomed:
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Ergomed is a specialized mid-size pharmacovigilance service provider, established in 2008, and is part of the Ergomed group. With a commitment to global organic growth, Ergomed has built a strong presence across Europe, North America, and Asia, offering services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance. The company prides itself on maintaining long-lasting relationships with pharmaceutical and biotechnology partners, covering all therapy areas, including medical devices. Ergomed values its employees by investing in their training and development, promoting well-being and mental health, and fostering a healthy work-life balance to ensure high-quality client service.
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Save This Job!
Jobs from Ergomed:
Senior Pharmacovigilance Physician
PV Auditor
PV Associate - Czech Speaker
PV Auditor
Senior Pharmacovigilance Officer
The Clinical Research Associate II is responsible for monitoring clinical trials and ensuring compliance with regulatory standards in Turkey.
The Clinical Research Associate II will assist in clinical studies, ensuring compliance and high-quality data reporting.
Join PSI as a Clinical Research Associate II to conduct monitoring tasks and manage clinical studies in various therapeutic areas.
Join PSI as a Clinical Research Associate II to manage clinical studies and ensure quality standards.
Join a flexible and supportive team as a Clinical Research Associate, focusing on quality monitoring and site management.