Clinical Research Associate I – ENT

Children's Minnesota

Clinical Research Associate supporting pediatric clinical research at Children’s Minnesota, a not-for-profit children’s health system. Coordinating studies, regulatory submissions, patient visits, and research data.

Posted 8/19/2026full-timeRemote • Minnesota, Wisconsin • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research processes, including study startup, implementation, and closeout activities, while ensuring compliance with Good Clinical Practice guidelines. Proficient in data management, regulatory submissions, and patient interaction for informed consent and data collection.

Highest-signal resume keywords

Clinical Research ExperienceRegulatory SubmissionsGood Clinical Practice ComplianceData ManagementPediatric Population Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

PhlebotomySample CollectionData EntryAdverse Event ReportingChart AbstractionECG AdministrationRegulatory Binder MaintenanceResearch Data CoordinationResearch Visit SchedulingInformed Consent Process

Soft Skills

Attention to DetailStrong Written CommunicationStrong Oral CommunicationAbility to MultitaskInterpersonal Skills

Tools & Technologies

Common Software SystemsData Management Software

Certifications & Qualifications

Occupational Health AssessmentDrug ScreenBackground Investigation

Industry Keywords

Institutional Review BoardFederal ComplianceLocal Agency ComplianceClinical ResearchGood Clinical Practice

About the role

Key responsibilities & impact

Perform study startup, implementation, and closeout activities
Assist the research team with coordination and entry of research data
Assist with regulatory submissions to the Institutional Review Board
Maintain compliance with federal and local agencies according to Good Clinical Practice guidelines
Interact with patients and families to secure informed consent, schedule research visits, and collect data
Maintain regulatory binder documentation, adverse event reporting, and sponsor-site communications
Perform assigned special research-area duties such as phlebotomy, sample collection, processing or shipping, ECGs, and chart abstraction
Manage personal career development and administrative tasks

Requirements

What you’ll need

Baccalaureate degree or at least 4 years relevant clinical research, professional experience
High attention to detail
Strong written and oral communication skills
Strong computer skills beyond basic familiarity with common hardware and software systems
Ability to assist staff working on multiple projects
Experience working with pediatric populations preferred
Successful completion of an occupational health assessment, drug screen, and background investigation
Compliance with the U.S. Government Form I-9, Employment Eligibility Verification

Benefits

Comp & perks

Medical, dental, vision, retirement, and other fringe benefits
Shift differentials or premium pay may be available for positions requiring night, weekend, or on-call work
Equal opportunity employment