Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
• Prepares, reviews and coordinates, under guidance, local regulatory submissions
(MoH, EC, additional special national local applications if applicable, e.g. gene
therapy approvals, viral safety dossiers, import license) in alignment with global
submission strategy.
• Provides, under guidance local regulatory strategy advice (MoH &/or EC) to
internal clients.
• Provides project specific local SSU services and coordination of these projects.
• May have contact with investigators for submission related activities.
• Key-contact at country level for either Ethical or Regulatory submission-related
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activities.
• 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 work with the start-up CRA(s) to prepare the regulatory compliance review
packages, as applicable.
• May develop country specific Patient Information Sheet/Informed Consent form
documents.
• May assist with grant budgets(s) and payment schedules negotiations with sites.
• Supports the coordination of feasibility activities, as required, in accordance with
agreed timelines.
• Entes and maintains trial status information relating to SIA activities onto PPD
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.