LAVORO STUDY SITE MONITOR CLINICAL

Investigator site relationships... organization to oversee fsp scp and site monitor roles... this role provides line management and oversees the site care partner...

• prior clinical experience preferred... • gain experience in study procedures by working with experienced clinical staff... assist in tracking subject site recruitment...

site activation partner - fsp - (, , remote) sign up with scientific... clinical trial site activation • initiate and coordinate activities and essential documents...

Good clinical practice (gcp) and international conference on harmonization (ich) guidelines)... job overview perform monitoring and site management work to ensure...

Job description as a  clinical research associate  at psi italy you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic...

site intelligence team... minimum 4 years relevant experience in clinical trials environment and clinical site activation... clinical trial management systems (ctms)...

Actively may participate in site feasibility and/or site qualification visit... external interfaces: investigators and their delegates at site (trial site personnel)...

O co-lead and oversee clinical development/authorship of informed consent forms, ecrfs, study manuals, clinical study reports, and regulatory submission documents...

Contributes significantly to the development of study documentation including clinical trial protocols and clinical study reports... demonstrates detailed understanding...

clinical research associate (sr... support site staff in preparation for study related site audits and inspections... and study specific training meetings...

Keywords: project manager, clinical project manager, cro, clinical research organisation, contract research organisation, clinical...