TRABAJO CLINICAL TRIAL ASSOCIATE START MADRID, MADRID

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...

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

Excellent understanding of the clinical study process including monitoring... reports study progress/update to the global study associate director/ global study...

Deep knowledge of international clinical trial regulations (ich-gcp, fda, ema)... supervise clinical trial monitoring, investigational product handling, and patient...

Responsible for the monthly us gaap trial balance review process... responsible for monthly review for activities to ensure a robust review of monthly trial balance...

Iqvia is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries...

Html what you will do: in your new role, you will start with a familiarization phase with product and clinical trainings to learn about our portfolio and build...

Extensive experience as a clinical research associate, with a strong understanding of clinical trial processes and regulatory requirements...

You will play a critical role in supporting site start-up and clinical trial operations across international studies... provide regular updates to clinical leadership...

We are currently seeking an in-house clinical research associate (ihcra) to join our diverse and dynamic team... in-house cra icon plc is a world-leading healthcare...