RASSU Spec II (Madrid)

RASSU Spec II (Madrid)

07 sep
|
Cti Clinical Trial And Consulting Services
|
Madrid

07 sep

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

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

Postulate a este anuncio

Muestra tus habilidades a la empresa, rellenar el formulario y deja un toque personal en la carta, ayudará el reclutador en la elección del candidato.

Suscribete a esta alerta:

Recibe por email las nuevas ofertas de trabajo para: rassu spec ii (madrid) / madrid