Role**: As a member of the Study Start Up Team, you will play an integral role in making sure that physicians... - Bachelor’s Degree preferably in Life Sciences - Minimum of 1 years’ experience or understanding of clinical study start up...
**: - As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites...’s degree preferably in Life Sciences - Minimum of 1 years’ experience or understanding of clinical study start up requirements...
requirements - Compiling and assessing completeness of the Regulatory-Package for drug release (Regulatory Document Study Start Up... of any findings - Review and adapt study specific documents according to each country and site requirements - Perform IRB/EC...
future of clinical development We are currently seeking a Study Start Up Associate I to join our diverse and dynamic team.... As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring...
Clinical Trial Associate (CTA) supports SSO Study Start-Up Manager and SSO Clinical Project Manager in assigned studies... during set-up and whole study lifecycle in compliance with Novartis processes, GCP/ICH and regulatory requirements...
while adhering to all applicable regulatory requirements, SOPs and ICH GCP - Assist with or oversee study start-up activities... Affairs Study Start-up Team in the preparation or revision of documentation for submission to Ethics Committee...
in all stages of the clinical study, including identifying potential sites, performing start-up activities (regulatory documents...OverviewSenior Clinical Research Associate - Oncology - Chile - RemoteJoin to apply for the Senior Clinical Research...
identifying potential sites to participate in the research effort, performing various study start-up activities such as working... of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every...
clinical study, including identifying potential sites to participate in the research effort, performing various study start-up... will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide...
Company. We are searching for the best talent for Site Manager to be in Buenos Aires, Argentina. Purpose: An Associate...), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure...
you could have! #GCO The Clinical Trial Associate (CTA) supports SSO Study Start-Up Manager and SSO Clinical Project Manager in assigned... studies during set-up and whole study lifecycle in compliance with Novartis processes, GCP/ICH and regulatory requirements...