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Clinical Research Coordinator II
Mass General Brigham. Support the team in enrolling eligible patients on oncology clinical trials .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in coordinating oncology clinical trials, including patient enrollment, scheduling, and compliance with protocols. Proficient in data management and communication with healthcare providers and patients to ensure successful trial execution.
Highest-signal resume keywords
Oncology Clinical Trials CoordinationPatient Enrollment SupportData Management ProgramsAnalytical SkillsClinical Research Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Patient ScreeningProtocol ComplianceVital Signs MeasurementEKG AdministrationQuality-of-Life Assessments
Soft Skills
Team CollaborationIndependent WorkProblem ResolutionCommunication Skills
Tools & Technologies
Clinical Safety Laboratory SystemsData Acquisition Tools
Industry Keywords
Clinical TrialsOncologyResearch ExperienceBWHMGH
About the role
Key responsibilities & impact- Support the team in enrolling eligible patients on oncology clinical trials
- Assist the Clinical Research Manager with implementation of clinical trials across different disease specialties at the BWH site
- Screen potential patients for study participation
- Schedule protocol-required tests, procedures, patient appointments, and clinical safety laboratory specimen draws
- Coordinate patient appointments with physicians, nurses, and test areas
- Ensure timely availability of laboratory results to providers
- Prepare pre-visit communication for providers
- Maintain point-of-contact communication with enrolled patients and assist with study participation questions
- Develop protocol-specific flow charts, intake sheets, and other tools for protocol compliance and data acquisition
- Coordinate, obtain, process, and ship protocol-required tissue samples
- Ensure collection and processing of correlative research blood samples with MGH and BWH processing labs
- Obtain vital signs and perform EKGs as required
- Administer quality-of-life assessments
- Scan research documents and certify them as copies
Requirements
What you’ll need- Bachelor's Degree required
- Related post-bachelor's degree research experience 1-2 years required
- Ability to work more independently and as a team member
- Computer literacy
- Analytical skills
- Ability to resolve technical problems
- Ability to interpret the acceptability of data results
- Working knowledge of data management programs
- Ability to perform duties on-site at both BWH and MGH locations as needed
Benefits
Comp & perks- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums
- Bonuses as applicable
- Recognition programs
- Reasonable accommodation for individuals with disabilities