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Children's Minnesota

Clinical Research Associate – Cancer and Blood Disorders

Children's Minnesota

Clinical Research Associate supporting pediatric research projects at Children’s Minnesota. Collaborating with healthcare professionals and contributing to regulatory compliance and data management.

Posted 7/16/2026full-timeMinnesota, Wisconsin • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical research processes, including study startup, implementation, and closeout activities, while ensuring compliance with regulatory standards. Proficient in data management, patient interaction, and documentation maintenance within research settings.

Highest-signal resume keywords
Clinical Research ExperienceRegulatory SubmissionsData ManagementPhlebotomy SkillsPediatric Population Experience

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical ResearchData EntryRegulatory ComplianceGood Clinical PracticePhlebotomySample CollectionAdverse Event ReportingChart AbstractionECGStudy Implementation
Soft Skills
Attention to DetailWritten CommunicationOral CommunicationTeam CollaborationMulti-Project Management
Tools & Technologies
Research SoftwareData Management SystemsRegulatory Binder ToolsScheduling Software
Industry Keywords
Institutional Review BoardInformed ConsentPediatric ResearchClinical TrialsFederal Compliance

About the role

Key responsibilities & impact
  • Support the research team in the conduct of department research projects
  • Perform study startup, implementation, and closeout activities
  • Assist research team with coordination and entry of research data
  • Assist with regulatory submissions to the Institutional Review Board, and maintain compliance with all federal and local agencies in accordance with Good Clinical Practice guidelines
  • Interact with patients and families for securing informed consent, scheduling research visits, and collection of data
  • Maintain documentation for regulatory binder, adverse event reporting, and communications between sponsors and sites
  • Other special skills specific to assigned research area may include phlebotomy, sample collection, processing or shipping, ECGs, chart abstraction or other duties as assigned
  • 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 with strong written and oral communication skills
  • Strong computer skills beyond basic familiarity with the most common hardware and software systems
  • Ability to assist staff working on multiple projects
  • Experience working with pediatric populations (preferred)

Benefits

Comp & perks
  • Medical, dental, vision, retirement, and other fringe benefits