Clinical Research Coordinator I, Head and Neck

Mass General Brigham•Boston, MA

3d•Onsite

About The Position

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. 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 Advanced Cutaneous Malignancies. 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
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.
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- Technical computer skills (Microsoft Office, Epic, MATLAB, Python, etc. preferred
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
1-2 years of relevant work experience (e.g., basic science, previous CRC experience, etc.) required for the CRC II position.
Previous animal handling experience is preferred but not required.
Other work experience will be considered but is not required.

Nice To Haves

Previous animal handling experience is preferred but 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.