03.06.2024 | Full-time | PharmiwebDocuments, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies. Act as primary company contact for assigned trial sites, engaging with Investigator and Site Staff throughout the life
Uita-te mai târziu03.06.2024 | Full-time | Cluj-Napoca | PharmiwebTo promote rapport with the site and staff. Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebAcross more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. We are currently looking for talented Clinical Research Associates to join our sponsor's team
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebAcross more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. We are currently looking for talented Clinical Research Associates to join our sponsor's team
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebTo promote rapport with the site and staff. Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human
Uita-te mai târziu03.06.2024 | Full-time | Oradea | PharmiwebDocuments, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies. Act as primary company contact for assigned trial sites, engaging with Investigator and Site Staff throughout the life
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEmerging risk so that the appropriate follow-up action can be taken. Arm the primary site monitor with important information that will enable Sponsor to be the clinical partner of choice; allowing monitors to work differently with site staff and have more productive discussions with our Investigator
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEmerging risk so that the appropriate follow-up action can be taken. Arm the primary site monitor with important information that will enable Sponsor to be the clinical partner of choice; allowing monitors to work differently with site staff and have more productive discussions with our Investigator
Uita-te mai târziu03.06.2024 | Full-time | Craiova | PharmiwebDocuments, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies. Act as primary company contact for assigned trial sites, engaging with Investigator and Site Staff throughout the life
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEmerging risk so that the appropriate follow-up action can be taken. Arm the primary site monitor with important information that will enable Sponsor to be the clinical partner of choice; allowing monitors to work differently with site staff and have more productive discussions with our Investigator
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