TRABAJO REGULATORY SPECIALIST STUDY START

Job purpose/summarymanage essential regulatory documentation (as applicable) for submission across europe, namely using eu submission portal (ctis) and/or other...

study start up associate / contracts & budget specialist  at icon, it’s our people that set us apart... study start up associate / contracts & budget specialist ...

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 iias a member of the study start up team, you will play an integral role in making sure that physicians at our research sites are prepared...

Prepare site regulatory documents, reviewing for completeness and accuracy... inform team members of completion of regulatory and contractual documents for individual...

Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst...

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

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...

Reports study progress/update to the global study associate director/ global study team including smm lead... assists in forecasting study timelines, resources,...

• accountable for study budget management (and re-forecasting where required) through the study lifecycle... • develop and maintain relevant study plans as well...

Global study management plan and its relevant components such as study project plan spp) including required input into study level quality and risk management planning...

Data acquisition specialist     purpose:     • the principal data acquisition specialist implements data collection requirements into validated...

Clinical study protocol (csp) through to clinical study report (csr)) in accordance with relevant az sops... • develop and maintain relevant study plans including...

study team meetings, monitors’ meetings, investigators’ meetings... • coordinates administrative tasks during the study process, audits and regulatory inspections...

Protocols/amendments, informed consent form (icf) documents detailing study delivery data management activities, etc... this role provides matrix management of functional...

Identify regulatory risks and communicate mitigations to regulatory lead and cross functional teams... review documents and provide regulatory input (e... accountabilities/responsibilities:...

G study protocols, periodic safety reports, etc... ) identify regulatory risks and communicate mitigations to regulatory lead and cross functional teams...   accountabilities/responsibilities...