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Clinical Research Coordinator II - Dermatology

MEDICAL COLLEGE OF WISCONSIN INC.

Milwaukee, WI · HybridFull-timePosted 1mo agoStill listed today

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At a glance

Compensation
No compensation found
Location
Milwaukee, WIHybrid
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

CITI Training Within 90 Days, required

Job overview

The Clinical Research Coordinator II supports day-to-day administrative activities for clinical research trial programs, helping the team achieve program goals. The role coordinates participant recruitment and research protocols, manages data and regulatory documentation, and monitors timelines and budgets. It also collaborates with investigators and other departments on program materials, outreach, and research resources.

Skills & qualifications

RequiredNice to have

Skills

Biology, nice to haveChemistry, nice to haveMathematics, nice to haveDocumentation, nice to haveRecords Management, nice to haveData Utilization, nice to haveComplex Problem Solving, nice to haveCritical Thinking, nice to haveResource Management, nice to haveWriting, nice to haveLifting Moderate Weight, nice to haveStanding, nice to haveWalking, nice to haveCommunication, nice to haveColor Discrimination, nice to haveDistance Perception, nice to have

Qualifications

Bachelor's Degree, required2 Years Experience, requiredCITI Training Within 90 Days, required

Benefits

Medical Insurance
Vision Insurance
Dental Insurance
401(k) Match
Paid Time Off
Tuition Assistance
Parental Leave

Full job description

Summary Perform the day-to-day administrative activities of clinical research trial programs. Provide support to the team to facilitate the achievement of the program’s goals. Assist with recruiting, training, and supervising staff and managing the program budget.

Primary Responsibilities

  • Recruit, screen, enroll and obtain consent from program participants. Conduct or coordinate training for program participants.
  • Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants.
  • Collect, analyze, and disseminate research data. Report program data and progress to study investigators. Work with Principal Investigator to develop, implement, and maintain comprehensive databases and files related to the program.
  • Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators.
  • Assure compliance with all relevant IRB and other regulatory agency requirements.
  • Prepare IRB documents and reports. Evaluate and write of research protocols in collaboration with the study investigator.
  • Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports.
  • Maintain program timeline including tracking deadlines for program components.
  • Coordinate program outreach activities including acting as a liaison with community organizations. Organize internal and external meetings, site visits, and special events.
  • Monitor study related budgets. Participate in the development of program resources through literature searches, contact with outside programs, and review of funding opportunities.
  • Other duties as assigned.

Knowledge – Skills – Abilities

  • Knowledge of biology, chemistry, mathematics, documentation, and records management.
  • Data utilization, complex problem solving, critical thinking, resource management, and writing skills.

Qualifications Appropriate experience may be substituted for education on an equivalent basis.

Minimum Required Education: Bachelor’s degree Minimum Required Experience: 2 years

Required Certification/Licensure(s): CITI training within 90 days of hire Preferred Certification/Licensure(s):

Physical Requirements Work requires occasionally lifting moderate weight materials, standing, or walking continuously.

Work Environment Occasional exposure to dust, noise, temperature changes, or contact with water or other liquids. Work is performed in an environmentally controlled environment.

Sensory Acuity Ability to detect and translate speech or other communication required. May occasionally require the ability to distinguish colors and perceive relative distances between objects.

#LI-NL1

Why MCW?

  • Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental. Along with 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.

For a brief overview of our benefits see: Benefits Overview

For a full list of positions see: MCW Careers

At MCW all of our endeavors, from our internal operations to our interactions with our partners, are driven by our shared organizational values: Caring – Collaborative – Curiosity – Inclusive – Integrity – Respect. We are committed to fostering an inclusive environment that values diversity in backgrounds, experiences, and perspectives through merit-based processes and in alignment with all applicable laws. We believe that embracing human differences is critical to realize our vision of a healthier world, and we recognize that a healthy and thriving community starts from within. Our values define who we are, what we stand for and how we conduct ourselves at MCW. If you believe in embracing individuality and working together according to these principles to improve health for all, then MCW is the place for you. For more information, please visit our institutional website.

MCW as an Equal Opportunity Employer and Commitment to Non-Discrimination:

The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer. We are committed to fostering an inclusive community of outstanding faculty, staff, and students, as well as ensuring equal educational opportunity, employment, and access to services, programs, and activities, without regard to an individual's race, color, national origin, religion, age, disability, sex, gender identity/expression, sexual orientation, marital status, pregnancy, predisposing genetic characteristic, or military status. Employees, students, applicants or other members of the MCW community (including but not limited to vendors, visitors, and guests) may not be subjected to harassment that is prohibited by law or treated adversely or retaliated against based upon a protected characteristic.

How this job compares

Set against the 645 open Clinical Research Coordinator jobs on Olive Jobs, counted November 10, 2026.

Pay
  • This postingNot listed
  • US median$56–75K/yr159 salary ranges
  • US median$24–36/hr196 hourly ranges
Openings
Olive Jobs lists 51 open Clinical Research Coordinator jobs in Wisconsin and 645 across the US. 2% of them nationwide are listed as remote or flexible.
Hiring the most in Wisconsin
Experience
This posting asks for at least 2 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (429 postings).
Education
188 of the 645 open Clinical Research Coordinator jobs (29%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 10, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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