In this role, you will build focus on line management and mentoring of Monitors on project-specific activities.
Hybrid workstyle at either Tokyo or Osaka office.
The scope of responsibilities will include:
- Prepare, conduct and report site selection, initiation, routine monitoring and closeout visits.
- Act as a Mentor for the Monitors on project-specific activities and supporting their professional development.
- Plan and conduct supervised monitoring visits with training, authorization, and ongoing assessment purposes.
- Build and maintain good relationships with sites’ staff involved in the study conduct.
- Contribute to the performance appraisal of monitors.
- Training, coaching and mentoring the Clinical Operations team.
- Supervise activities of Site Management Associates related to the flow of documents and laboratory supplies between the site and the Central/Regional Laboratory/Central Reviewer.
- Development and implementation of quality control, ensuring data integrity and compliance at a site level.
- Ensure proper handling, accountability and reconciliation of all Investigational Products and clinical study supplies.
- Supports Clinical Operations Managers with resource allocation and
utilization of departmental staff
- Performs additional Clinical Operations supervisory tasks at the discretion of
their Line Manager