TRABAJO CLINICAL TRIALS ASSISTANT MADRID, MADRID

Basic knowledge of applicable clinical research regulatory requirement, i... assist the clinical team with the preparation, handling, distribution, filing, and archiving...

• knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i...

The clinical trial learning and development (ctl&d) organization develops and delivers learning strategy, design, and operations for johnson & johnson and...

Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time...

Alcobendas (madrid) (madrid)empresa: lillyrequisitos: bachelor’s degree or equivalent work experience in a scientific field or health-related field with no less...

Job description performs on-site or remote pre-study, initiation, interim, and close-out monitoring visit activities to ensure that facilities and staff at the...

clinical trial management system)... with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our...

Deep knowledge of clinical trials regulations... safety protocols and procedures for clinical research studies... the development safety update report (dsur) for...

Review documents related to clinical trials and post-authorization safety studies where the r&d departments... provide input to benefit risk-assessments and clinical...

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our...

Iqvia is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry...

Learn how to conduct trials and evaluations of product in theatre and clinical environment as required... html key responsibilities start to gain an understanding...

Take responsibility for the p&r or hta dossier preparation and submission to health authorities, understanding payers’ requirements and needs translating them in...

Provide input to benefit risk-assessments and clinical expert statement as applicable... review documents related to clinical trials and post-authorization safety...

clinical outcome assessment, patient-reported outcome, electronic implementation a plus)... clinical outcome assessments (coas)/patient-reported outcomes (pros)...

“ iqvia is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry...

As a clinical trial assistant at icon, you’ll work with a collaborative and successful team to support our clinical trial management and project management...