LAVORO REGULATORY CLINICAL TRIAL SUBMISSIONS

Prepares and/or reviews regulatory documents to support clinical trial submissions... independently provides regulatory support for complex projects and programs...

Maintains and updates trial management systems... the ltm ii is responsible for coordinating and leading the local trial team to deliver quality data and trial documents/records...

Maintains and updates trial management systems... the ltm iii is responsible for coordinating and leading the local trial team to deliver quality data and trial...

Basic knowledge of applicable clinical research regulatory requirement, i... senior clinical trial administrator, single sponsor dedicated - milan   job overview:...

Basic knowledge of applicable clinical research regulatory requirement, i... senior clinical trial administrator, single sponsor dedicated - milan job overview:...

Prepares and/or reviews regulatory documents to support clinical trial submissions... prepares and maintains core clinical trial submission dossiers in accordance...

Perform/support submissions activities to swissmedic through the appropriate electronic gateway and support client during the entire regulatory process...

As a ctaii at allucent, you act as the primary administrative support to allucent clinical study teams at country/site level, support clinical trial operations and...

Overview: the head emea regulatory affairs strategy organization is a member of the global regulatory affairs organization... develops regional regulatory strategic...

Director clinical scientist provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and...

The clinical scientist provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and clinical...

Develops regional regulatory strategic objectives, goals and performance measures... reporting relationships: reports to vp head emea regulatory affairs strategy...

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

·       may review/co-author medical publications emerging from clinical trial results... knowledge of good clinical practices and...

Purpose -    support the clinical team in relevant medical and scientific aspects of the assigned global clinical studies within the global clinical development...

Facilitate communication between clinical sites and other abbott clinical staff (e... proactively and critically examine ways to enhance overall clinical trial performance...

They are looking for a clinical affairs program manager europe... overall responsibility for design of clinical trials including protocol development, clinical trial...

Prior regulatory authority experience desirable... provides strategic regulatory advice towards efficient clinical development and navigation of us & european regulatory...

For consistency with case report forms as well as monitor clinical trial/study safety, in keeping with protocols, gcp (good clinical practices), phi (personal health...