Facilitates site selection process by conducting meetings with appropriate departments and individuals to review and revise draft site list as necessary, and by communicating the final site list to team members.
May 21, 2023
Demonstrated ability to deliver results to the appropriate quality and timeline metrics.
October 14, 2022
Requires 8 years total experience preferably in Clinical Affairs, Program Management and/or Regulatory.
November 21, 2022
Demonstrates mastery of current business unit therapeutic environment and drug development trends and facilitates the development of knowledge for more junior staff.
December 20, 2022
Maintains effective communication with the Customer and project team through oral and written correspondence, project status reports, and monthly progress reports.
January 26, 2023
Produces and distributes status, resourcing, and tracking reports as well as functional area plan to customers, appropriate team members and senior management.
March 22, 2023
Lead the completion of study files and ensure success of global clinical trials.
April 09, 2023
Provide project oversight to ensure that studies are completed on time, within budget and in compliance with SOPs, FDA and global regulations and ICH/GCP guidelines.
May 20, 2023
