Senior Clinical Research Coordinator

Mass General Brigham

. Support the team in enrolling eligible patients in oncology clinical trials .

Posted 10/27/2026full-timeBoston • Massachusetts • United StatesSenior💰 $27 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating oncology clinical trials, managing patient enrollment, and ensuring compliance with clinical research regulations. Proficient in data management and communication, with a strong ability to mentor and train staff.

Highest-signal resume keywords

Oncology Clinical Trials CoordinationData Management SkillsClinical Research CompliancePatient Enrollment SupportInterpersonal Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research OperationsProtocol ComplianceData AnalysisVital Signs MeasurementEKG AdministrationQuality-of-Life AssessmentsAdministrative Task ManagementResearch Document CertificationPatient ScreeningFlow Chart Development

Soft Skills

Time ManagementOrganizational SkillsTeam CollaborationInitiativeMentoring

Tools & Technologies

Data Management SystemsClinical Safety Laboratory ToolsResearch Documentation Software

Industry Keywords

Clinical ResearchOncologyStandard Operating ProceduresCompliance ProcessesPatient CoordinationResearch Trends

About the role

Key responsibilities & impact

Support the team in enrolling eligible patients in oncology clinical trials
Support clinical research operations at Brigham and Women’s Hospital and Massachusetts General Hospital
Assist the Clinical Research Manager with implementation of clinical trials across different disease specialties at the BWH site
Schedule protocol-mandated tests required for compliance with institutional and federal clinical research regulations
Assist management with Standard Operating Procedure changes and compliance processes
Train new staff
Manage studies within a specialized program
Perform disease-specific administrative tasks
Screen potential patients for study participation
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 front-line study questions
Develop protocol-specific flow charts, intake sheets, and tools for protocol compliance and data acquisition
Coordinate, obtain, process, and ship protocol-required tissue samples
Coordinate processing of required correlative research blood samples with MGH and BWH processing labs
Obtain vital signs and perform EKGs as required
Administer quality-of-life assessments
Scan and certify research documents as copies

Requirements

What you’ll need

Bachelor's Degree Required
Related post-bachelor's degree research experience 3-5 years required
Ability to work more independently and as a team member
High degree of computer literacy and analytical skills
Ability to identify both technical and non-technical problems and develop solutions
Ability to interpret the acceptability of data results
Highly proficient data management skills and working knowledge of data management systems
Able to display initiative to introduce innovations to research studies
Excellent time management, organizational, interpersonal, written, and verbal communication skills
Knowledge of current and developing clinical research trends
Sound interpersonal skills and the ability to mentor others
Ability to work independently and display initiative

Benefits

Comp & perks

Comprehensive benefits
Career advancement opportunities
Differentials
Premiums
Bonuses as applicable
Recognition programs
Reasonable accommodation for qualified individuals with disabilities