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Clinical Research Coordinator
Mass General BrighamClinical Research Coordinator supporting Mass General Brigham’s cancer detection and diagnostics studies. Enrolling patients, coordinating protocol procedures, processing samples, and managing clinical research data.
Posted 8/5/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesMid-LevelSenior💰 $21 - $29 per hourWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in coordinating clinical research activities, including patient enrollment, data management, and compliance with clinical research protocols. Proficient in maintaining accurate research documentation and effective communication with patients and healthcare professionals.
Highest-signal resume keywords
Clinical Research CoordinationData Entry and ManagementPatient EnrollmentREDCap Database ManagementAttention to Detail
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Data Acquisition ToolsClinical Research ProtocolsPatient Demographics ExtractionSpecimen ProcessingElectronic Medical Record Review
Soft Skills
Good Organizational SkillsInterpersonal CommunicationAbility to Follow DirectionsProfessionalismFlexibility
Tools & Technologies
REDCapElectronic Medical Records
Industry Keywords
Clinical ResearchPatient SafetyResearch ProtocolsTissue Sample CoordinationAmbulatory Care
About the role
Key responsibilities & impact- Support the Cancer Early Detection and Diagnostics research team in enrolling eligible patients into clinical research protocols
- Schedule protocol-mandated tests and procedures
- Coordinate patient appointments with physicians, nurses, and test areas
- Coordinate clinical safety laboratory specimen draws and ensure timely results
- Prepare pre-visit communications for providers
- Maintain point-of-contact communication with enrolled patients and answer frontline study-participation questions
- Develop protocol-specific flow charts, intake sheets, and data-acquisition tools
- Coordinate, obtain, process, and ship tissue samples
- Ensure collection and processing of correlative research blood samples with the MGH Sample Processing Lab
- Scan and certify research documents
- Follow patients throughout study participation via electronic medical record review
- Extract patient demographics and clinical data through chart review and complete data entry
- Maintain research charts and electronic files
- Ensure adequate source documentation and resolve data queries
- Build and maintain REDCap databases
- Maintain screening and enrollment logs
- Coordinate analysis of collected materials with clinical and research laboratory personnel
- Attend research team meetings
Requirements
What you’ll need- BA/BS degree required
- Bachelor's Degree in a related field required
- Some relevant research project work preferred (0–1 year)
- Careful attention to detail
- 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
- Flexibility to commute to MGH Boston, MGH Waltham, and Brigham Women’s Hospital
- Ability to work in an ambulatory/clinical office setting
Benefits
Comp & perks- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums
- Bonuses as applicable
- Recognition programs
- Professional growth support
- Reasonable accommodation for applicants with disabilities