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MCW

Clinical Research Coordinator

MCW

. Perform day-to-day administrative activities of the clinical research trials program .

Posted 9/17/2026full-timeWauwatosa • Wisconsin • United StatesJuniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical research administration, including participant recruitment, protocol coordination, and compliance with IRB and regulatory requirements. Proficient in data analysis, problem-solving, and effective communication with stakeholders.

Highest-signal resume keywords
Clinical Research AdministrationParticipant RecruitmentIRB ComplianceData AnalysisProtocol Coordination

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
Biology KnowledgeChemistry KnowledgeMathematics KnowledgeDocumentation ManagementRecords ManagementData UtilizationComplex Problem SolvingCritical ThinkingWriting SkillsCITI Training
Soft Skills
Resource ManagementCommunication Skills
Tools & Technologies
Comprehensive Program Databases
Certifications & Qualifications
Associate's DegreeCITI Training
Industry Keywords
Clinical Research TrialsResearch ProtocolsStakeholder ReportingCommunity OutreachRegulatory Agency Requirements

About the role

Key responsibilities & impact
  • Perform day-to-day administrative activities of the clinical research trials program
  • Provide support to facilitate achievement of the program’s goals
  • Recruit, screen, enroll, and obtain consent from program participants
  • Conduct or coordinate training for program participants
  • Coordinate research protocols, appointments, procedures, and participant contact
  • Collaborate with departments and institutions
  • Collect, analyze, and disseminate program data
  • Report program data and progress to stakeholders
  • Identify protocol implementation problems and communicate them to study investigators
  • Assure compliance with IRB and regulatory agency requirements
  • Assist with preparation of IRB documents and reports
  • Assist in evaluation and writing of research protocols
  • Collaborate on educational, marketing, website, form, and report materials
  • Develop, implement, and maintain comprehensive program databases and files with the Principal Investigator
  • Maintain program timelines and track deadlines
  • Coordinate outreach activities and liaise with community organizations
  • Perform other duties as assigned

Requirements

What you’ll need
  • Knowledge of biology, chemistry, mathematics, documentation, and records management
  • Data utilization, complex problem solving, critical thinking, resource management, and writing skills
  • Associate's Degree required
  • Appropriate experience may be substituted for education on an equivalent basis
  • Minimum 1 year of experience
  • CITI training within 90 days of hire
  • Ability to occasionally lift moderate weight materials, stand, or walk continuously
  • Ability to detect and translate speech or other communication
  • May occasionally require the ability to distinguish colors and perceive relative distances between objects

Benefits

Comp & perks
  • Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental
  • Flexible Spending options
  • 403B Retirement Package
  • Competitive Vacation and Paid Holidays offered
  • Tuition Reimbursement
  • Paid Parental Leave
  • Employee & Family Assistance Program (EFAP)
  • Pet Insurance
  • On campus Fitness Facility, offering onsite classes
  • Additional discounted rates on items such as: Select cell phone plans, local fitness facilities, Milwaukee recreation and entertainment etc.