TRABAJO REGULATORY SPECIALIST STUDY START BARCELONA, BARCELONA

study start up associate / contract specialist at icon, it’s our people that set us apart... study start up associate ii as a member of the study start up team...

study start up associate ii at icon, it’s our people that set us apart... responsibilities:   perform a variety of routine essential document collection, review...

Provides matrix management of functional area representatives to cross functional clinical study teams... protocols/amendments, informed consent form (icf) documents...

Support the study team in the implementation of audits and regulatory inspections... support risk management and quality efforts to ensure study compliance...

• experience in all phases of a clinical study lifecycle... • extensive knowledge of clinical research regulatory requirements (incl ich-gcp) and demonstrated abilities...

(inter)national coordinating investigators, steering/executive committee) during study design and delivery   manage study finance:    develop and maintain the overall...

Prepare and provide input to clinical study reports (csrs) and clinical portions of regulatory documents (e... responsible for timely responses to investigational...

study level: supports the study lead or in some instances serves as the clinical lead for the study guides aspects of the cdp, aligning study protocols, and ensuring...

Ensures study systems are complete, accurate and updated per agreed study conventions (e... responds to company, client and applicable regulatory requirements/audits/inspections...

The scope of work includes, but is not limited to, clinical study report development, regulatory submissions, commercialization, and the scientific utilization of...

You will provide subject matter expertise within the programming discipline and act as a specialist within cross-functional teams to deliver continuous improvement...

Identify high potential growth projects: • study new acquisition channels and/or market opportunities (internally or externally) like google ads, meta ads, tik tok...

It is a bridge between study site operations (sso) clinical trials and medical affairs, aligning technical, operations & strategy... • reporting of technical complaints...

As the key web development specialist within the team, you’ll be responsible for the scaffolding, design and implementation of modern javascript-based in-browser...