Clinical Trial Assistant- Sponsor Dedicated
... Local Study Team (LST) the Clinical Trial Assistant ensures quality and consistency ... preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking ...
Trabajo Clinical Trial Monitor en España. Se encontraron 8582 las vacantes nuevas en esta región
Clinical Research Associate II
... the role of a typical clinical monitor. CRA’s are accountable for using ... efficacy and drug accountability. Execute. Monitor the completeness and quality of ... to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document ...
Clin Research Coordinator II- Barcelona (Spain)
... for the study. Clinical ConductPerform all study activities following Good Clinical Practices (GCP). Manage multiple clinical trials simultaneously. Protect the safety of human subjects. Monitor appropriate sources for specific clinical study or federal ...
Clinical Trial Coordinator Assisted reproduction and gynaecological endocrinology Unit_20240156
... are developing a clinical trial to demonstrate the safety and ... updating of the clinical trial electronic notebook and for the ... Project Manager of the clinical trial sponsor to monitor the progress of the clinical trial and or possible incidents related ...
Clinical Research Associate II - Ophthamology - Spain
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
Clinical Research Associate III - Ophthamology - Spain
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
Clinical Quality Compliance Lead
... strategic plan based on upcoming clinical trial activities and Quality Management Review( ... all stakeholders involved in the clinical trial conduct process Coach internal and ...
Sr. Clinical Research Associate (Spain)
... , you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with ...
Clinical Research Associate III - Ophthamology - Spain
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...
Clinical Research Associate III - Ophthamology - Spain
... Responsibilities: Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation. Monitor ...