Clinical Research Program Manager

Mass General Brigham•Boston, MA

1d•Onsite

About The Position

Responsible for managing a clinical study involving multiple sites around the world. This includes leading efforts on selecting and testing site capabilities for long-term compliance, engaging in and managing contractual agreements with sites, and training staff on study protocols and data upload to a web-based data collection system. The role also involves generating standard operating procedures and working directly with investigators, clinicians, software developers, and other lab personnel.

Requirements

Bachelor's Degree Related Field of Study required
Research Related Experience 3-5 years required
Excellent critical thinking skills and ability to work independently are essential.
Must be self-motivated and able to work independently.
Good verbal and written communication skills.
Proficiency in Word, Power point, Excel.
Ability to make independent effective decisions.
Strong organizational skills.
Demonstrated analytical skills to problem solve effectively.

Responsibilities

Engages potential sites and tests their capabilities for long-term compliance.
Trains the site coordinators at each clinical site.
Monitors the site coordinators at each clinical site.
Trains newly hired technical staff to work on this project.
Responsible for the generation and maintenance of standard operating procedures.
Responsible for communicating project progress with the sponsor.
Responsible for troubleshooting problems related to access the web based registry.
Prepares reports and presents progress at research staff meetings.