RASSU Spec II (Madrid)

RASSU Spec II (Madrid)

31 ago
|
Cti Clinical Trial And Consulting Services
|
Madrid

31 ago

Cti Clinical Trial And Consulting Services

Madrid

What You’ll Do

Assist/Advise project teams on all regulatory requirements for clinical studies
Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings
Review and adapt study specific documents according each country and site requirements
Perform IRB/EC (CA) and/or other Regulatory Bodies submissions on behalf of sponsors and/or sites as agreed with the Sponsor and in accordance with each country requirements
Receive and process study documentation from sites, check content and quality as well as completeness
Interact with site personnel, CPCs, CRAs and PMs for document corrections, clarification or resolution of any incomplete and/or incorrect documentation found during document content quality review
Compile Regulatory documentation according to CTI SOPs, sponsor SOPs and applicable country requirements, perform a QC review of all documentation before submitting to the sites, IRB/EC/CA and/or other Regulatory Bodies according to the local requirements




Assist with and adapt Informed Consent Form (ICF) according to IRB/IEC requests on country or site level
Assist in preparation, quality check and filing of site adapted ICF according to local requirements
Prepare and QC Clinical Trial Application forms (e.g. CTA, XML) where applicable
Interact with Sponsors as needed; forward regulatory documentation, including final regulatory submission packages, if requested, to Sponsor in accordance with CTI or Sponsor SOPs
Respond to Deficiency Letters from IRB/IEC/CA and/or other Regulatory Bodies in liaison with sponsor and study PM or assist sites in their response to IRB according to country and site requirements
Compiling and assessing completeness of the Regulatory-Package for drug release (Regulatory Document Study Start Up Checklist)
Provide Project teams with accurate periodic status reports in accordance with CTI SOPs and attend internal and external project meetings as needed
Accura

📌 RASSU Spec II (Madrid)
🏢 Cti Clinical Trial And Consulting Services
📍 Madrid

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