TRABAJO CLINICAL STUDY MANAGER

clinical operations department duties\/responsibilities... serves as a source of clinical research expertise for iqvia biotech clinical staff... ","applicantlocationrequirements":[{"@type":"country"...

•    responsible for development and ongoing maintenance of clinical study tools and templates, including the clinical monitoring plan... •    demonstrates understanding...

•    responsible for development and ongoing maintenance of clinical study tools and templates,  including the clinical monitoring plan... •    demonstrates understanding...

Strong knowledge of clinical research processes related to study start-up... facilitates communication with the clinical team (e... ensure project level compliance...

Opportunities available for an experienced clinical trial manager ii or senior clinical trial manager... develop and implement clinical monitoring plan... ","applicantlocationrequirements":[{"@type":"country"...

Job summary the clinical supply chain manager is responsible for the strategic planning and execution of new clinical trial supply chains...

•    responsible for study management components of inspection readiness for all aspects of the study conduct...   •    clinical research organization (cro) and...

Iqvia biotech is now hiring a study start-up manager... this position works directly with clinical monitoring, project management and clinical trial managers in...

Contacting clinical trial participants remotely (e... clinical outcome assessments (coas)\/patient-reported outcomes (pros), preference research) and passive (e...

Iqvia is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry... ","applicantlocationrequirements":[{"@type":"country"...

Company description psi is a leading contract research organization with more than 25 years in the industry, offering a perfect balance between stability and innovation...

We focus on delivering quality and on-time services across a variety of therapeutic indications... company description psi is a leading contract research organization...

• good understanding of clinical study management including monitoring, study drug handling and data management... • manages study supplies (isf, etc), drug supplies...

Delivery of study milestones esp... co-own start-up phase and the recruitment plan for development clinical trials with the study & site operations organization...

Responsible for review of synopses, other relevant clinical study documents and critical study results... accountabilities:  accountable to oncology clinical science...

Quality oversight of clinical trials, including clinical trial protocol development, execution, and submissions... thorough understanding of clinical r&d activities...

• collects, reviews, and monitors required regulatory documentation for study start-up, study  maintenance and study close-out...   • good understanding and working...

clinical data programmer icon plc is a world-leading healthcare intelligence and clinical research organization... clinical data programmer location: mexico city...

• 3+ years of clinical research experiences as a: clinical trial assistant or study coordinator... • may lead cta study teams... • knowledge of applicable clinical...