Clinical Research Coordinator I, Head and Neck

Mass General Brigham•Boston, MA

22h•$21 - $29•Onsite

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.; and maintaining and updating data generated by the study. The Clinical Research Coordinator (CRC) works under the supervision of the Principal Investigator (PI), to provide support for clinical research studies. A major focus of this research is clinical research in the field of Head and Neck Radiation Oncology and Functional Radiation Medicine. The CRC will be responsible for: assisting the PI in drafting research protocols, patient enrollment and coordination, data entry, management, and analysis, creation and maintenance of clinical databases, preparation of conference presentations and journal publications.

Requirements

Bachelor's Degree Related Field of Study required
Some relevant research project work 0-1 year preferred
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Nice To Haves

Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.
Previous animal handling experience is preferred but not required.
Other work experience will be considered but is not required.

Responsibilities

Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
Recruiting patients for clinical trials and conducting phone interviews.
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.
Assist with data abstraction from a variety of sources including patient medical records, radiation treatment software, and hospital clinical information systems.
Assist with data analysis and system evaluation.
Assist with grant progress reports and IRB submissions as needed.
Organizes, and/or maintains study databases. Responsible for data entry and quality control of data.
Assists with analysis of clinical data
Coordination of patient visits for research protocols
Collection of patient reported data
Performs literature searches as appropriate.
Assists PI with preparation of slide presentations, meeting posters, and research articles.
Performs all other duties as assigned.