♦ Assist with the formulation of instructional materials and training of investigators, study coordinators and associated study site personnel on the conduct of the clinical trials, as applicable

♦ Assist Study Manager with safety monitoring including preparing supporting documentation for CEC and/or DSMB, meetings, agenda, data review, presentations, and updating relevant trackers as applicable.

♦ Serve as a point of contact between clinical site investigators and the MiRus team.

♦ Work with investigators and site personnel to quickly and effectively resolve discrepancies.

♦ May be responsible for patient accruals and tracking payments to sites for clinical study programs.

♦ Monitor ongoing compliance to study protocols in accordance with applicable regulations and GCP, work instructions, guidelines and/or policies.