SPR-886 | Country Approval Associate

SPR-886 | Country Approval Associate

07 feb
|
Thermo Fisher Scientific
|
Nuevo Casas Grandes

07 feb

Thermo Fisher Scientific

Nuevo Casas Grandes

**Work Schedule**Other**Environmental Conditions**OfficeEssential Functions- Prepares, reviews and coordinates, under guidance and local EC submissions in alignment with global submission strategy.- Supports preparation, under guidance, of local MoH submissions, as applicable in alignment with global submission strategy.- Coordinates, under guidance,



with internal functional departments to ensure various site start-up activities are aligned with submissions activities and mutually agreed upon timelines; ensures alignment of submission process for sites and study are aligned to the critical path for site activation.- Achieves PPD's target cycle times for site.- May have contact with investigators for submission related activities.- May act as a key-contact at country level for either Ethical or Regulatory submission-related activities.- Works with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable.- Assists in developing country specific Patient Information Sheet/Informed Consent form documents.- Assists with grant budgets(s) and payment schedules negotiations with sites.- Enters and maintains trial status information relating to SIA activities onto PPD, or client (where contracted) tracking databases in an accurate and timely manner- Ensures the local country study files and filing processes are prepared, set up and maintained as per PPD WPDs or applicable client SOPs.- Maintains knowledge of and understand PPD SOPs, Client SOPs/directives, and current regulatory guidelines as applicable to services provided.

El anuncio original lo puedes encontrar en Kit Empleo:
https://www.kitempleo.com.mx/empleo/139082672/spr-886-country-approval-associate-nuevo-casas-grandes/?utm_source=html

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