TRABAJO CLINICAL TRIAL ASSOCIATE START

Investigator’s brochures, health authority briefing books, safety updates, submission dossiers, and responses to health authorities) in collaboration with appropriate...

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

Familiarity with ich-gcp, gdpr, mdr, and local spanish clinical trial regulations is important... later, you might join calls with clinical trial managers and divisional...

Extensive experience as a clinical research associate, with a strong understanding of clinical trial processes and regulatory requirements... what you will be doing:monitoring...

Analyze clinical trial data to support strategic decisions and regulatory submissions... skilled in analyzing and presenting complex clinical data... main responsibilities:contribute...

As a ssu associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence...

We are looking for a clinical research associate (cra ii) to join our a-team (hybrid)... as a cra ii at allucent, you will independently control and monitor investigational...

• superior clinical research operational knowledge... • partner with the global trial lead to execute and oversee central activities from planning, trial start up...

\u superior clinical research operational knowledge... \u years clinical trial management experience in the pharmaceutical industry or cro... \u strong project planning\/management...

Understanding of scientific and clinical issues related to the design and implementation of clinical trials and interpreting trial results particularly in respiratory...

Escalates cra performance issues to applicable clinical trial oversight manager... supports and contributes to clinical study teams (csts) / trial management teams...

Proficiency in clinical trial management systems (ctms) and start-up tracking tools... extensive experience in study start-up or clinical operations, with a strong...

Contributes to the selection of vendors for the outsourcing of clinical trial services... working relations:  core study team global clinical lead / clinical development...

Strong monitoring experience in oncological clinical trials... position summary: the manager clinical monitoring (gcm) offers an additional development path for...

Ideal background would be vendor manager, global project management associate/associate project manager, associate study manager... investigators’/monitors&rsquo...

Provide good clinical practice (gcp) guidance to day-to-day questions arising from clinical trials deliverables... strong skills in gcp, quality and/or clinical...

    you must be able to start by end of august... informed consent form, master clinical study agreement etc), and external service provider related documents...