LAVORO CLINICAL STUDY ADMINISTRATOR

Minimum 2 years of experience as a clinical study associate/clinical trial assistant or study coordinator proven organizational and administrative skills...

We are currently recruiting for a clinical director oncology (principal scientist) to join our european clinical development (ecd) team... requisition id: r...

General description: accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget leads the regional...

Experience managing clinical project team personnel... experience leading operational teams through the start-up, study conduct, data management, and report writing...

As a clinical research associate at psi italy, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining...

#li-ces #li-dnp iqvia is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare...

Solid knowledge of clinical data management and... archiving of study cts related documentation in the company cts repository... #li-ces #li-dnp iqvia is a leading...

Experiencia mínima de 3 años en clinical monitoring... descripción del puesto: estamos buscando un clinical study manager altamente cualificado para una de las principales...

Site management); develops clinical trial documents (e... study protocol, informed consents, crf, monitoring plan, study manual, investigator brochure, annual reports)...

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

clinical research certification (acrp or socra, clinical coordinator/cra certification) preferred... key responsibilities: study start-up and study conduct activities...

Perform study close-out visits and archive study documentation and correspondence... perform study initiation activities, reviewing with the site personnel, the...

study protocol, informed consents, crf, monitoring plan, study manual, investigator brochure, annual reports), ensure registration on www... ability to travel approximately...

Our j&j medtech neurovascular clinical team is currently seeking a senior clinical research specialist... study protocol, informed consents, crf, monitoring plan...

Assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical study subject documentation...

Ensure the study is registered on public clinical trial registries (e... ideally experience managing respiratory clinical trials... clinical trial supplies: collaborate...

Ensure the study is registered on public clinical trial registries (e... clinical trial supplies: collaborate with the clinical trial supply coordinator to establish...

Description our j&j medtech neurovascular clinical team is currently recruiting for a clinical research manager... clinical project leadership across multiple studies/...