1.    

Assumes a role in implementing clinical research trials with internal and external groups to accomplish research objectives.

    2.    

Will provide assurance of compliance with clinical and research regulations.

    3.    

Contributes to the preparation of clinical protocols, study reports, and any relevant regulatory document submissions. 

    4.    

Assists in patient recruitment, provides informed consent, data collection, and correspondence with various internal hospital and external research departments.

    5.    

Provides education, instruction, and actively addresses questions and concerns from patients.

    6.    

Orders supplies needed to conduct research and maintains inventory of supplies.

    7.    

Maintains a clean working area and adheres to proper safety techniques and procedures.

    8.    

Must demonstrate an ability to manage multiple responsibilities, act independently and communicate effectively across team lines.

    9.    

Performs miscellaneous related duties.