Wer wir sind

ÜBER ENOVIS™

Who We Are

ABOUT ENOVIS™

Was Sie tun werden | What You'll Do

Oversees the direction, planning, execution and interpretation of clinical trials/research and data collection activities along with regulatory compliance, patient safety and emerging patient risks. May establish and approve scientific methods for design and implementation of clinical protocols, data collection systems and final reports. Provides input on clinical study design, execution, and data analysis. Leads the adverse event reporting and safety responsibilities monitoring. Coordinates and develops information for reports submitted to regulatory agencies. Monitors adherence to protocols and determines study completion. May recruit clinical investigators and negotiate study design and costs. May act as consultant/liaison with other corporations when working under licensing agreements. Establishes strategic plans and o...