Responsible for the preparation of local EC submissions and supporting the preparation of MoH (ISP) submissions, as appropriate, according to the submission strategy.
As applicable, coordinate with others internal functional departments to ensure activities aligned with the submission and site activation strategy and according to the agreed timelines.
Responsible for preparing and reviewing country and site-specific informed consent forms documents.
Also have contact with the investigators and the study coordinators for activities related to submissions and act as a key contact at country level for Ethical or Regulatory submission related activities.
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