TRABAJO CLINICAL TRIAL ASSOCIATE FLUENT

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

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...

At least 3 years' experience within clinical trials and study operations specific therapeutic experience in cns and oncology, will be desirable comprehensive knowledge...

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...

As a clinical trial strategy and operations manager at novartis, you’ll be accountable for bringing global and hub strategies to life at the country level—translating...

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...

Contributes to the selection of vendors for the outsourcing of clinical trial services... fluent in english, both written and spoken... understands the asset’s biological...

? your role & impactas a senior clinical project manager, you'll:lead end‑to‑end trial delivery, collaborating closely with clinical ops managers/senior trial managers...

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

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

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

Informed consent form, master clinical study agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions...

clinical trial support:  provide technical support for clinical trial activities within the assigned territory, including site authorization and study procedures...

clinical trial support:  provide technical support for clinical trial activities within the assigned territory, including site authorization and study procedures...