TRABAJO QUALITY COMPLIANCE CLINICAL EXPERT MADRID, MADRID

As the europe quality director, you will ensure rigorous compliance with internal and external policies, standards, certifications, and procedures related to quality...

Experience with clinical trial management systems (e... ) and clinical document control systems / etmf... support internal quality audits, regulatory inspections...

Basic knowledge of applicable clinical research regulatory requirement, i... essential functions: assist clinical research associates (cras) and regulatory and start-up...

clinical trial team leader... • adhere to chubb's ethical, service standards and quality... the clinical trial team leader will act as a knowledge resource on clinical...

·   write and revise quality management procedures as required... ·   organize and deliver training to other iqvia departments concerning the activities of quality...

clinical trial manager - sponsor dedicated (global) icon plc is a world-leading healthcare intelligence and clinical research organization... collaborate with cross-functional...

clinical trial hub coordinator... • act as a knowledge resource point on clinical trials for underwriters on specifics of clinical trial issuance...

quality awareness in high extend... documenting results in the plant's quality assurance system... assessing compliance with legal regulations and abbott requirements...

Your key responsibilities:as a payments product expert in payments clearing you will:provide a broad knowledge on ing products, services, channels, and local payments...

Key collaborators are the clinical lead for site management, the project vendor manager, the project management analyst for project coordination, tracking and financial...

Your key responsibilities:as a daily payments digital business expert in payments clearing you will:provide a broad knowledge on ing products, services, channels...

Com       process expert manager     position:   the it bts sales & tm process expert manager acts as a liaison between business and development teams in order to...

clinical trials experience and good understanding of clinical trial data and study design (desirable)... provides clinical presentations and medical information...

Good understanding and working knowledge of clinical research, phases of clinical trials, current gcp/ich & country clinical research law & guidelines...

Primary responsibilities: responsible for executing clinical studies in compliance with quality standards (ich/gcp, global regulations, and abbvie policies andprocedures)...

Complete periodic quality reviews and peer feedback reports... ensure compliance of budgetary guidance, templates and process... with clinical trials conducted in...