EMPREGO CLINICAL TRIAL COORDINATOR WITH

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

Supports inspection readiness for clinical trial management scope...    reviews the project oversight dashboards and other clinical trial systems (e...

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

•    good understanding of clinical trial process across phases ii-iv and ich gcp... job responsibilities  •    provide support with site selection lead and project...

Experience in clinical trial planning and conduct... experience of leading global phase ii-iii clinical trials, with experience in oncology or adaptive/innovative...

•    meet slas and ad hoc project and cross project queries from trial teams and management with minimal guidance... •    build and maintain effective working...

Represent clinical development on project teams... job summary  (primary function) this position is responsible for working with the physicians within clinical development...

• advise, consult and make final recommendations to all aspects of clinical regulatory intelligence...  the company is committed to compliance with the americans...

Prepares and maintains core clinical trial submission dossiers in accordance with applicable regulatory requirements... prepares and/or reviews regulatory documents...

Prepares and/or reviews regulatory documents to support clinical trial submissions... thank you for your interest in growing your career with us...

Purpose prepares and/or reviews regulatory documents to support clinical trial submissions... thank you for your interest in growing your career with us...

Work collaboratively with the data management, clinical operations, medical writing and the pharmacovigilance team as appropriate... review the clinical study report...

Thank you for your interest in growing your career with us... · 3 years of prior relevant experience including experience managing clinical trial safety/post-marketing...

⦁    works with clinical trial managers to review or prepare of clinical trial reports and summary documents that support the regulatory needs of a project...

•    extensive knowledge of english grammar with a familiarity with ama style guide...   •    ability to demonstrate a familiarity with principles of clinical...