Clinical Research Coordinator

The Opportunity:

Our location in Alameda, California has an opportunity for an experienced professional in the Medical Affairs Sub-Function, who possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.

What you will do:

•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.

Requirements:

Must have an Associate's Degree in a relatable field of study

0-2 years of experience in a similar role.