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Clinical Research Coordinator II Obgyn

MCW: SARGEANT HEALTH CENTER

MILWAUKEE, WIJobSeen 2w agoSeen in employer's feed 2 days ago

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At a glance

Compensation
No compensation found
Location
MILWAUKEE, WI
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, required

Job overview

The Clinical Research Coordinator II supports the day-to-day administration of clinical research trial programs and helps the team achieve program goals. The role coordinates participant recruitment and study protocols, manages research data and regulatory documentation, and monitors timelines and budgets. It also collaborates with investigators, departments, institutions, and community organizations to support research activities.

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 have

Qualifications

Bachelor's Degree, required2 Years Experience, requiredCITI Training, required

Full job description

JOB REQUIREMENTS: 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 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... For full info follow application link. EEO/AA Minorities/Females/Vets/Disability The Medical College of Wisconsin is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, veteran status, disability or sexual orientation. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/A9B95BB3C7F74D81 Qualified females, minorities, and special disabled veterans and other veterans are encouraged to apply.

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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