systems. Facilitates site budgets and contract negotiations. Supports site regulatory document collection.... Under supervision, may prepare initial submission dossiers to competent authorities, ethics committees, and/or site submission dossiers...
systems. Facilitates site budgets and contract negotiations. Supports site regulatory document collection.... Under supervision, may prepare initial submission dossiers to competent authorities, ethics committees, and/or site submission dossiers...
SSU kick off meeting. Country level: maintain country level contract templates Site level: create and maintain site... CSA review and negotiations with key site. Subject injury claim and insurance procedure support. Organize the study...
process. As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol... and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial...
as cookies used to display content tailored to your interests. Your experience of the site and the services we are able... Jobs Job Description Apply now Start Please wait... Job Title: ANALYST DIGITAL MKTG II Posting Start Date: 12/22/25 At TE, you will unleash...
Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON...CRA II, Shanghai, Office with Flex ICON plc is a world-leading healthcare intelligence and clinical research...
, etc.). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP... future. Summarized Purpose: Performs and coordinates different aspects of the clinical monitoring and site management...
, etc.). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP... future. Summarized Purpose: Performs and coordinates different aspects of the clinical monitoring and site management...