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Clinical Research Coordinator I
Mass General BrighamClinical Research Coordinator assisting with clinical research studies at Mass General Brigham. Responsibilities include patient recruitment, data organization, and compliance verification in research protocols.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research processes, including patient recruitment, data collection, and compliance with regulatory standards. Proficient in maintaining accurate documentation and ensuring adherence to clinical research protocols.
Highest-signal resume keywords
Clinical Research ProtocolsPatient RecruitmentData CollectionRegulatory CompliancePhlebotomy
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 EntryClinical TestingPatient SchedulingQA/QC ProceduresDocumenting Patient Visits
Soft Skills
Attention to DetailOrganizational SkillsInterpersonal SkillsCommunication SkillsAbility to Follow Directions
Tools & Technologies
Computer Literacy
Industry Keywords
Clinical ResearchPatient ConsentStudy ProposalsRegulatory BindersStudy Subject Interviews
About the role
Key responsibilities & impact- Provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies
- Collecting and organizing patient data
- Scheduling patients for study visits
- Performing clinical tests such as phlebotomy, EKGs, etc.
- Maintaining and updating data generated by the study
- Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met
- Preparing data for analysis and data entry
- Documents patient visits and procedures
- Assists with regulatory binders and QA/QC Procedures
- Assists with interviewing study subjects
- Assists with study regulator submissions
Requirements
What you’ll need- Bachelor's Degree Related Field of Study required
- Some relevant research project work 0-1 year preferred
- 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
Benefits
Comp & perks- Competitive base pay
- Comprehensive benefits
- Career advancement opportunities
- Differentials, premiums and bonuses as applicable
- Recognition programs designed to celebrate your contributions and support your professional growth