Research Coordinator – BLES

The Geneva Foundation

Research Coordinator assisting Principal Investigator in clinical research activities at Ft. Bragg and Fayetteville.

Posted 7/29/2026part-timeFt. Bragg • North Carolina • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in research coordination, data collection, and adherence to regulatory guidelines such as OSHA, GCP, and GLP. Proficient in managing research protocols and effectively communicating with diverse stakeholders.

Highest-signal resume keywords

Research CoordinationData CollectionClinical Research ExperienceCommunication SkillsMicrosoft Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data AnalysisReport GenerationProject Close-Out SupportResearch Protocol ImplementationInfection Control ProceduresGood Clinical PracticesGood Laboratory PracticesCFR KnowledgeICH Guidelines

Soft Skills

Organizational SkillsAttention to DetailPositive DemeanorFlexibilityDiplomatic Communication

Tools & Technologies

ExcelMicrosoft Office Software

Industry Keywords

Occupational Safety and Health AdministrationNon-Profit ResearchHealthcare ExperienceResearch Subjects Coordination

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Assist with report generation and project close-out support
Perform data collection responsibilities as assigned
Promote safety and confidentiality of research participants at all times
Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data
Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives
Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives
Document all correspondence and communication pertinent to the research
Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization

Requirements

What you’ll need

Bachelor’s degree or equivalent work experience required
U.S. Citizenship required
Research coordination and data collection experience highly desired
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

Benefits

Comp & perks

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year
up to 4 weeks of paid time off in a rolling year