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Clinical Research Associate III
Clinical Research Associate IIISunrise Systems • Milwaukee, Wisconsin, United States
Clinical Research Associate III

Clinical Research Associate III

Sunrise Systems • Milwaukee, Wisconsin, United States
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Note- this contract is 100% onsite so please only submit local candidates to the below address in WI.


Title Clinical Research Coordinator


Number of Leased Workers needed 1

Tentative start date asap

Tentative end date 12 months

Work shift (days/times) 1st Shift

Work Location 100% onsite, 9900 W. Innovation Dr., Wauwatosa, WI 53226

Travel Required (% of travel) No, just to office each day

Is this a temp to perm position Contract only


Posted Position Title


Clinical Research Coordinator


Role Summary/Purpose


The Clinical Research Coordinator is responsible for managing in-house clinical research for the Client Ultrasound Businesses


Essential Responsibilities

Duties include (but are not limited to):


Recruit, screen, enroll, and obtain informed consent from study participants

Coordinate and oversee research sessions, including scheduling participants, reserving space, ensuring staff training, and managing documentation

Ensure compliance with the study protocol, external standards (regulations, GCP, IRB requirements), and internal Client processes

Maintain all study documentation, including regulatory binders, source documentation, trackers, and other materials

Complete IRB submissions such as new study submissions, Continuing Review, Amendments, Deviation reports, and Adverse Event reports

Conduct training and provide guidance to a large study staff

Facilitate regular monitoring visits; prepare for audits as needed

Serve as main point of contact for research volunteers and study staff

Maintain facilities (consent area, scan bays), order supplies and track spend

Implement process improvement activities as needed

Implement electronic processes to facilitate compliance and efficiency

Provide support to Research Program Integrators as needed

Serve as a Subject Matter Expert (SME) for coordinators at global sites executing similar protocols


This role requires physical presence in the Client Research Park facility in Wauwatosa, WI during ultrasound scanning sessions.


Qualifications/Requirements


1. Bachelor's degree in science or research-related field

2. Previous experience with a minimum of 2 years in clinical research

3. Outstanding organizational skills

4. Proficient at Microsoft Office (Excel, Outlook, Word)

5. Meticulous attention to detail

6. Exceptionally well-organized

7. Excellent communication skills (written and verbal)

8. Must be willing to work in our Wauwatosa, WI facility



Desired Characteristics


1. CCRC or CCRP certified preferred

2. Previous experience as a Clinical Research Coordinator

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