Works with Regulatory Affairs, Clinical Operations and Field Assurance to ensure timely reporting of AEs, SAEs and UADEs including expedited and annual reporting and other documents as needed.
March 20, 2023
Collaborates with data management and other departments on the development of case report forms, study specific safety reports, and other study specific forms.
March 22, 2023
Contribute to CIP (Clinical Investigational Plan) ICF (Informed Consent Form), eCRF (Case Report Form), and CSR (Clinical Study Report) development.
August 18, 2022
Reviews daily all incident reports submitted and works with applicable managers as needed for review/investigation of reports.
January 30, 2023
Prepares reports and analysis of clinical safety events and audits data in order to identify opportunities for clinical process improvement initiatives.
March 13, 2023
Develops, implements and evaluates educational plans/programs and utilizes methods, measurements and tools to evaluate achievement of learning goals.
March 14, 2023
Maintains distinctive quality and commitment as the operating philosophy in carrying out all processes.
March 22, 2023