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Clinical Research Coordinator Interstitial Lung Disease Program

Brigham and Women's Hospital
United States, Massachusetts, Boston
20 Shattuck Street (Show on map)
Oct 02, 2025
The Interstitial Lung Disease Program (ILD) at Brigham is seeking a highly organized and motivated individual with interest in clinical research to join our research program as a full-time Clinical Coordinator under supervision of the of the Principal Investigator and Project Manager, and working in collaboration with the research team. The incumbent will be responsible for supporting all aspects of clinical trial coordination for ILD research projects. The position is expected to begin around October 2025 with some flexibility on the start date. A CRC I or II may be hired based on level of experience and skills.
Summary
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 and files; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, vitals etc.; maintaining and updating data generated by the study.
Does this position require Patient interaction? Yes
Essential Functions
Reviews proposals for compliance with sponsor and organizational guidelines; verify all sponsor requirements are met.
-Recruiting patients for clinical trials, conducts phone interviews.
-Verifies the accuracy of study forms and updates them per protocol.
-Prepares data for analysis and data entry.
-Schedule, coordinate and documents patient visits and procedures.
-Administer questionnaires
-Conducts monitor visits
-Schedule all protocol-required tests and procedures
-Maintain point of contact communication with enrolled patients
-Develop protocol-specific flow charts, intake sheets, and other tools to ensure protocol compliance and proper data acquisition
-Coordinate, obtain, process, and ship protocol-required samples
-Work cross functionally with the departments involved in the project
-Assists with regulatory binders and QA/QC Procedures.
-Assists with interviewing study subjects.
-Assists with study regulator submissions.

Education
Bachelor's Degree Science required

Experience
Some relevant research project work 0-1 year preferred

Knowledge, Skills and Abilities
- 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.



The Brigham and Women's Hospital, Inc. is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
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