Study Coordinator I

Cayuse Holdings

. Provide services to government-led clinical and translational studies .

Posted 10/6/2026full-timeHonolulu • Hawaii • United StatesJuniorMid-Level💰 $25 - $27 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical and translational studies, including data collection, statistical analysis, and manuscript preparation. Proficient in collaborating with multidisciplinary teams and communicating complex data effectively.

Highest-signal resume keywords

Clinical Trial ExperienceStatistical Data AnalysisManuscript PreparationBiomedical Science DegreeMicrosoft Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ManagementData CollectionPatient Data OrganizationSpecimen ProcessingChart ReviewStudy Subject MonitoringStatistical AnalysisReport WritingPolicy DevelopmentLaboratory Analysis

Soft Skills

Oral CommunicationWritten CommunicationProblem-SolvingTeam CollaborationIndependent Work

Tools & Technologies

Microsoft ExcelMicrosoft WordMicrosoft PowerPointAdobe Acrobat

Industry Keywords

Clinical ResearchTranslational StudiesPatient Eligibility ReviewData DisseminationResearch Oversight

About the role

Key responsibilities & impact

Provide services to government-led clinical and translational studies
Work directly with the Principal Investigator/designated point of contact
Collect, organize, maintain, and disseminate patient data files
Review patient records for study eligibility
Screen, enroll, and monitor study subjects
Obtain specimens for laboratory analysis
Conduct chart reviews and specimen processing
Manage clinical study data
Interact with physicians, scientists, nurses, and laboratory personnel
Perform statistical data analysis
Prepare oral and written presentations based on data analysis and study summaries
Prepare written reports of findings and manuscripts for publication
Manage multiple clinical and translational studies simultaneously
Develop policies and procedures for clinical study execution and oversight
Report to the Director of Research
Perform other duties as assigned

Requirements

What you’ll need

Minimum Bachelor of Science in Biomedical science field or nursing
Biomedical degree with clinical or translational experience
Minimum 2 years clinical trial or laboratory study experience
Familiarity with statistical analysis and preparing manuscripts for publication
Must be able to pass a background check; additional checks may be required by projects or clients
Ability to communicate well orally and in writing using technical and nontechnical language
Ability to process and apply diverse and complex amounts of data
Problem-solving skills
Proficient in Microsoft and Adobe toolsets, including Excel, Word, PowerPoint, and Acrobat
Ability to work independently and as part of a team
Must be able to lift 20 lbs.
Must be able to work on-site in Honolulu, Hawaii
Must be able to sit for long periods while looking at a computer screen
May be asked to work outside normal business hours

Benefits

Comp & perks

Medical, Dental and Vision Insurance
Wellness Program
Flexible Spending Accounts (Healthcare, Dependent Care, Commuter)
Short-Term and Long-Term Disability options
Basic Life and AD&D Insurance (Company Provided)
Voluntary Life and AD&D options
401(k) Retirement Savings Plan with matching after one year
Paid Time Off
Flexible schedule may include holidays
Business travel or professional development opportunities