Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
MCW

Clinical Research Coordinator II

MCW

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

Posted 10/14/2026full-timeWauwatosa • Wisconsin • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in coordinating clinical research trials, including participant recruitment, data analysis, and compliance with regulatory requirements. Proficient in managing program timelines and collaborating with various stakeholders to achieve program goals.

Highest-signal resume keywords
Clinical Research CoordinationParticipant RecruitmentData AnalysisIRB ComplianceCITI Training

ATS Keywords

Tailor your resume
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 Skills
Soft Skills
CollaborationCommunicationResource Management
Tools & Technologies
Program DatabasesResearch Protocols
Certifications & Qualifications
CITI Training
Industry Keywords
Clinical Research TrialsIRBStakeholder ReportingOutreach Activities

About the role

Key responsibilities & impact
  • Perform day-to-day administrative activities of the clinical research trials program
  • Support the team in achieving program goals
  • Recruit, screen, enroll, and obtain consent from program participants across primary care and specialty clinics and in the community
  • 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 and communicate problems related to research protocol implementation
  • Ensure compliance with IRB and other regulatory requirements
  • Assist with IRB submissions, documents, reports, research protocol evaluation, and writing
  • Collaborate on educational materials, marketing materials, websites, forms, and reports
  • Develop, implement, and maintain program databases and files with the Principal Investigator
  • Maintain program timelines and track deadlines
  • Coordinate outreach activities and act as a liaison with community organizations
  • Perform other duties as assigned

Requirements

What you’ll need
  • Bachelor’s degree
  • Minimum 2 years of experience
  • Appropriate experience may be substituted for education on an equivalent basis
  • CITI training within 90 days of hire
  • Knowledge of biology, chemistry, mathematics, documentation, and records management
  • Data utilization, complex problem solving, critical thinking, resource management, and writing skills
  • 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 Health, Vision, and Dental
  • Flexible Spending options
  • 403B Retirement Package
  • Competitive Vacation and Paid Holidays
  • Tuition Reimbursement
  • Paid Parental Leave
  • Employee & Family Assistance Program (EFAP)
  • Pet Insurance
  • On campus Fitness Facility, offering onsite classes
  • Discounted rates on select cell phone plans, local fitness facilities, Milwaukee recreation and entertainment