Manager Medical Information and Operations

MAIN RESPONSIBILITIES

. As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.

. Contributes to implementation of clinical protocols, and facilitates completion of final reports.

. Recruits clinical investigators and negotiates study design and costs.

. Responsible for directing human clinical trials, phases III & IV for company products under development.

. Participates in adverse event reporting and safety responsibilities monitoring.

. Coordinates and provides reporting information for reports submitted to the regulatory agencies.

. Monitors adherence to protocols and determines study completion.

. Coordinates and oversees investigator initiations and group studies.

. May participate in adverse event reporting and safety responsibilities monitoring.

. May act as consultant/liaison with other corporations when working under licensing agreements.

QUALIFICATIONS

Associates Degree

Minimum 1 year