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Research Coordinator
The Geneva Foundation. Provide assistance to the Principal Investigator and Study Team coordinating research activities .
Posted 10/23/2026full-timeHonolulu • Hawaii • United StatesMid-LevelSenior💰 $50,000 - $72,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in coordinating clinical research activities, including participant recruitment, data management, and adherence to regulatory guidelines such as GCP and OSHA. Proficient in communication and organization, ensuring effective collaboration with study teams and stakeholders.
Highest-signal resume keywords
Clinical Research CoordinationData ManagementRegulatory Compliance (GCP, OSHA)Participant RecruitmentOral and Written Communication
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 CollectionData AnalysisReport GenerationResearch Protocol ImplementationIntermediate Excel SkillsMicrosoft Office Software
Soft Skills
Organizational SkillsAttention to DetailPositive DemeanorFlexibility with PrioritiesDiplomatic Communication
Industry Keywords
CFR GuidelinesGCP GuidelinesICH GuidelinesInfection Control ProceduresNon-Profit Research Experience
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Provide assistance to the Principal Investigator and Study Team coordinating research activities
- Recruit research participants
- Collect and manage data
- Assist with report generation and project close-out support
- Promote safety and confidentiality of research participants
- Adhere to OSHA, GCP, GLP, and infection control procedures
- Plan and coordinate research study protocol initiation and implementation of operating policies and procedures
- Maintain data collection and analysis systems and coordinate research data collection and analysis
- Recruit, instruct, and coordinate research subjects and/or volunteers
- Coordinate day-to-day activities of technical support staff engaged in research/clinical protocols
- Organize and facilitate meetings, conferences, events, and outreach activities
- Document correspondence and communication pertinent to research
- Communicate with the Principal Investigator, site personnel, research participants, The Geneva Foundation, and the funding organization
Requirements
What you’ll need- Bachelor’s degree or equivalent work experience required
- 2-4 years’ experience in clinical research preferred
- 2-4 years’ non-profit, research, or healthcare experience desired
- Demonstrate competence in oral and written communication
- Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
- Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
- Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
- Knowledge of CFR, GCP and ICH guidelines