Senior Clinical Research Coordinator

Mass General Brigham

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

Posted 9/30/2026full-timeBoston • Massachusetts • United StatesSenior💰 $27 per hourWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in coordinating oncology clinical trials, including patient enrollment, compliance processes, and data management. Proficient in communication, time management, and problem-solving within a clinical research environment.

Highest-signal resume keywords

Oncology Clinical Trials CoordinationPatient EnrollmentData Management SkillsClinical Research ComplianceExcellent Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ExperienceProtocol DevelopmentData AnalysisVital Signs MeasurementEKG AdministrationQuality-of-Life AssessmentsSpecimen ProcessingResearch DocumentationTime ManagementAnalytical Skills

Soft Skills

Interpersonal SkillsMentoring AbilityProblem-SolvingInitiativeOrganizational Skills

Tools & Technologies

Data Management SystemsCompliance ToolsResearch Software

Industry Keywords

Clinical TrialsOncologyResearch ComplianceStandard Operating ProceduresPatient Coordination

About the role

Key responsibilities & impact

Support the team in enrolling eligible patients on oncology clinical trials
Work as a CRC at Brigham and Women’s Hospital and assist the Clinical Research Manager with implementing clinical trials across disease specialties
Schedule all protocol-mandated tests required for institutional and federal research compliance
Assist management with Standard Operating Procedure changes, compliance processes, training new staff, specialized program studies, and disease-specific administrative tasks
Screen potential patients for study participation
Coordinate patient appointments with physicians, nurses, and testing areas
Schedule 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 study participation questions
Develop protocol-specific flow charts, intake sheets, and compliance/data-acquisition tools
Coordinate, obtain, process, and ship required tissue samples
Collect and process 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

BA/BS degree required; Bachelor's Degree in a related field required
Related post-bachelor's degree research experience: 3–5 years required
2–4 years related experience
High-level time management and organization skills
Excellent written and verbal communication skills
Knowledge of current and developing clinical research trends
Sound interpersonal skills and ability to mentor others
Ability to work independently and display initiative
Ability to identify problems and develop solutions
High degree of computer literacy and analytical skills
Ability to interpret acceptability of data results
Highly proficient data management skills and working knowledge of data management systems
Ability to introduce innovations to research studies
Experience in lieu of a degree accepted

Benefits

Comp & perks

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