p>Required Skills: Accountability, Analytical Problem Solving, Clinical Data Management, Clinical IT, Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trial Management, Clinical Trials Monitoring, Clinical Trials Operations, Clinical Trial Support, Data Analysis, Drug Regulatory Affairs, ICH GCP Guidelines, Project Management, Regulatory Compliance.
Regulatory & Site Start-Up responsibilities - Collaborate with other country roles to:
In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions.