Clinical Research Coordinator I, Department of Urology

Mass General Brigham•Boston, MA

2d•Hybrid

About The Position

Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; maintaining and updating data generated by the study. The role involves reviewing proposals for compliance with sponsor and organizational guidelines, verifying sponsor requirements, recruiting patients for clinical trials, preparing data for analysis and entry, documenting patient visits and procedures, and assisting with regulatory binders, QA/QC procedures, interviewing study subjects, and study regulator submissions.

Requirements

Bachelor's Degree Science required
Some relevant research project work 0-1 year preferred
Careful attention to detail and good organizational skills.
Ability to follow directions.
Good interpersonal and communication skills.
Computer literacy.
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Responsibilities

Reviews proposals for compliance with sponsor and organizational guidelines; verify all sponsor requirements are met.
Recruiting patients for clinical trials, conducts phone.
Verifies the accuracy of study forms and updates them per protocol.
Prepares data for analysis and data entry.
Documents patient visits and procedures.
Assists with regulatory binders and QA/QC Procedures.
Assists with interviewing study subjects.
Assists with study regulator submissions.