LAVORO CLINICAL ASSOCIATE ITALY

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...

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...

Skills: cardiology, oncology, respiratory, clinical research associate, clinical trials, cro, medical devices, monitoring, pharma location: italy...

In-depth knowledge of gcp, ich guidelines, and regulatory requirements related to clinical trials... team collaboration: collaborate with cross-functional teams...

• prior clinical experience preferred... • advanced knowledge of applicable clinical research regulatory requirements, i... • some organizations may require 2 years...

Ensures site staff have current gcp and necessary protocol, compound and systems training to conduct the clinical trial... ensures clinical drug supplies are...

Internal job description experienced clinical research associate your responsibilities will include... experience in pharma industry, and\/or clinical trials environment...

Good clinical practice (gcp) and international conference on harmonization (ich) guidelines... • good knowledge of, and skill in applying, applicable clinical research...

Jsb solutions, società di servizi nel settore life science che offre consulenza, gestione di studi clinici e sviluppo software, con 3 sedi in italia (firenze, parma...

Good clinical practice (gcp) and international conference on harmonization (ich) guidelines)... req • good knowledge of, and skill in applying, applicable clinical...

Independent experience in on-site monitoring of clinical trials... being in possession of right to work in italy... #weareiqvia #projectpatientfocus #li-remote iqvia...

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

They are looking for a clinical affairs program manager europe... additional responsibilities include management of clinical trials approvals with local irbs and/or...

Who we are looking for purpose lead and coordinate the clinical monitoring of assigned clinical studies according to ich gcp, chiesi procedures and regulatory...

Cdc italy is responsible for conducting clinical trials within the country, providing clinical trial management and administration supporting the local teams...

Experience with clinical supply systems (e... the associate director, is a matrix team leader responsible for the management of clinical supplies during the study...