Reviews and submits protocol specific Informed Consent Form (ICF) if changes are required.
January 20, 2023
Actively participate in assigned disease team including maintaining ongoing communication with team leaders.
January 28, 2023
Maintains understanding of the professional guidelines and code of ethics related to clinical research conduct, and maintains ability to summarize and clarify these for study teams.
March 01, 2023
Works closely with sponsors and study teams on the preparation of regulatory documents and addressing relevant regulatory issues.
March 03, 2023
Complete all reviews and submissions in a timely manner, meeting all deadlines.
March 11, 2023
Assists in the performance of other regulatory functions within the Compliance section of the Regulatory department .
March 18, 2023
Participate in improving organizational performance through recommending areas or approaches for improvement activities, performing new procedures, collecting data and providing input to department discussions.
April 11, 2023