Demonstrated ability to work independently and collaborate effectively with physicians, coordinators, sponsors, and multidisciplinary teams.
Demonstrated ability to manage multiple priorities simultaneously and consistently meet deadlines in a fast-paced environment.
Strong verbal and written communication skills with demonstrated attention to detail and sound professional judgment.
Working knowledge of medical terminology.
Demonstrated organizational skills and proficiency with Microsoft Office applications, including Word and Excel.
Demonstrated problem-solving and conflict-resolution skills.
Ability to reliably travel between multiple work sites with dependable transportation.
Current ACRP or SoCRA Certification or ability to become certified within 6 months of hire
Nice to have
Health or science related college degree or equivalent education and experience.
Understanding of medical terminology
Previous experience working in a lab setting or with basic sample processing
Previous experience with research applications used in the UW CTI: OnCore, eBinders (Florence), Advarra Payments, EPIC, etc.
Experience with training staff
Experience working on at least one FDA regulated Clinical Trial
Experience working on industry sponsored clinical trials
Independent, proactive individual with minimal need for oversight
Full description
Current Employees: If you are currently employed at any of the Universities of Wisconsin, log in to Workday to apply through the internal application process.
Job Category:
Academic Staff
Employment Type:
Regular
Job Profile:
Clinical Research Coordinator I
Job Summary:
The Clinical Trials Institute (CTI) has an exciting opportunity for an entry-level or experienced, full-time clinical research coordinator to join our growing team. The ideal candidate is intrinsically motivated, detailed oriented, an enthusiastic problem solver, and works well in a multi-disciplinary team to achieve a common goal. This role directly interacts with current and prospective participants of all ages and backgrounds, so the successful applicant is a clear, compassionate communicator with a strong customer service attitude. Additional responsibilities of the role include executing the procedures of the research protocol, safeguarding the integrity of study data, and actively participating in the screening, recruitment, and retention of our clinical trial participants. Senior members of the team are also expected to lend their experience to assist in training and mentoring new and less experienced members of the team.
This is an on-site position with standard business hours expected during the workweek. However, studies may require a Coordinator remain on-site for an extended number of hours (e.g. 14) while a subject participates in an intervention period – must have flexible work schedule, able to work extended days (e.g. 14 hours), evenings, some holidays, and weekends. A remote day will be given during the probationary period, at the discretion of the supervisor. Additionally, the role may involve travel between research sites within the metro Madison area, so the incumbent should have reliable transportation or be willing to use public transportation. If you are ready to make a meaningful impact in the field of clinical research, we encourage you to apply today!
This position may require some work to be performed in-person, onsite, at a designated campus work location. Some work may be performed remotely, at an offsite, non-campus work location.
This position has been identified as a position of trust with access to vulnerable populations. The selected candidate will be required to pass an initial caregiver check to be eligible for employment under the Wisconsin Caregiver Law and every four years.
Applicants for this position will be considered for the following titles Clinical Research Coordinator I; Clinical Research Coordinator II. The title is determined by the experience and qualifications of the finalist.
Must provide a valid driver's license. Employees may use their own transportation or receive approval for University Car Fleet usage. Employment is conditional pending the results of a Pre-hire Driver Authorization Check. See https://businessservices.wisc.edu/managing-risk/driver-authorization-and-insurance/driver-authorization/#become-authorized-driver (click on “Become an authorized driver;” then click on “Required criteria”).
Clinical Research Coordinator I or II at wisconsin (Madison, WI) — aijobsearch
Candidates who demonstrate the following knowledge, skills, and abilities will be given first consideration: Knowledge of HIPPA requirements and aligned practices; Knowledge of GCP guidelines and regulatory compliance.
Key Job Responsibilities:
Participate in quality and process improvement endeavors within the CTI; contributes to the development of newworkflows and demonstrate flexibility in an evolving environment.
Reconcile research billing, payments, and invoices and financial issues in concert with CTI financial specialists.
Identifies resource needs and develops clinical research documents such as job aids, tools, processes, procedures,and training. Contributes to the development of protocols.
May assist with training staff.
Recruits, screens, selects, determines eligibility and enrolls trial participants, collects information, and answers questions under supervision of a medically licensed professional. May perform basic medical assessments after completion of required training/certification, such as collecting vital signs, obtaining weight, and performing phlebotomy
Serves as an initial point of contact for clinical research participants and clinical staff, providing information regarding research procedures, expectations, and informational inquiries. Ensures participants follow the research protocol and alerts Principal Investigator of issues
Schedules logistics, determines workflows, and secures resources for a defined clinical research trial(s)
Identifies work unit resources needs and manages supply and equipment inventory levels
Manages research workflow components, collects, prepares, processes, and submits participant data and samples to appropriate entities, adhering to research protocols
Performs quality checks.
Department:
School of Medicine and Public Health, UW Clinical Trials Institute
The UW Clinical Trials Institute (CTI), located in beautiful Madison, WI, supports clinical research professionals, participants, and industry partners to advance research in the prevention, detection, and treatment of disease to help improve the health of individuals, families, and communities across Wisconsin and beyond. Our talented staff facilitates the operation and execution of a variety of industry-sponsored and investigator-initiated clinical trials at the University of Wisconsin–Madison and UW Health. The CTI's culture is team-oriented where workplace environment is as important as the work we perform. We pride ourselves on being collaborative and supportive and value input and an open exchange of ideas. We hope you will consider joining us to help advance our mission to move medicine forward.
Compensation:
The starting salary for the position is $51,000 for a CRC I and $56,000 for a CRC II, but is negotiable based on experience and qualifications.
Employees in this position can expect to receive benefits such as generous vacation, holidays, and sick leave; competitive insurances and savings accounts; retirement benefits. For more information, refer to the campus benefits webpage.
SMPH Faculty /Academic Staff Benefits Flyer 2026
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Required Qualifications:
Demonstrated ability to work independently and collaborate effectively with physicians, coordinators, sponsors, and multidisciplinary teams.
Demonstrated ability to manage multiple priorities simultaneously and consistently meet deadlines in a fast-paced environment.
Strong verbal and written communication skills with demonstrated attention to detail and sound professional judgment.
Working knowledge of medical terminology.
Demonstrated organizational skills and proficiency with Microsoft Office applications, including Word and Excel.
Demonstrated problem-solving and conflict-resolution skills.
Ability to reliably travel between multiple work sites with dependable transportation.
Current ACRP or SoCRA Certification or ability to become certified within 6 months of hire
Preferred Qualifications:
Health or science related college degree or equivalent education and experience.
Understanding of medical terminology
Previous experience working in a lab setting or with basic sample processing
Previous experience with research applications used in the UW CTI: OnCore, eBinders (Florence), Advarra Payments, EPIC, etc.
Experience with training staff
Experience working on at least one FDA regulated Clinical Trial
Experience working on industry sponsored clinical trials
Independent, proactive individual with minimal need for oversight
Education:
Bachelor’s Degree preferred; focus in health or sciences related preferred
How to Apply:
For the best experience completing your application, we recommend using Chrome or Firefox as your web browser.
To apply for this position, select either “I am a current employee” or “I am not a current employee” under Apply Now. You will then be prompted to upload your application materials.
Important: The application has only one attachment field. Upload the following documents in that field, either as a single combined file or as multiple files in the same upload area. Failure to submit the required documents will result in no longer being considered for the position.
Cover letter
Resume
Your cover letter should address how your training and experience aligns with the required and preferred qualifications listed above. Application reviewers will rely on these written materials to determine which applicants move forward in the process. References will be requested from final candidates. All applicants will be notified once the search concludes and a candidate is selected.
University sponsorship is not available for this position, including transfers of sponsorship and TN visas. The selected applicant will be responsible for ensuring their continuous eligibility to work in the United States (i.e. a citizen or national of the United States, a lawful permanent resident, a foreign national authorized to work in the United States without the need of an employer sponsorship) on or before the effective date of appointment. This position is an ongoing position that will require continuous work eligibility and will require eligibility to work for the full duration of the appointment. If you are selected for this position, you must provide proof of work authorization and eligibility to work.
The department will not be able to support a request for a J-1 waiver. If you choose to pursue a waiver and apply for our position, neither the UW nor UWMF will reimburse you for your legal or waiver fees.
Contact Information:
Rochelle Rannow, rochelle.rannow@wisc.edu
Relay Access (WTRS): 7-1-1. See RELAY_SERVICE for further information.
Institutional Statement on Diversity:
Diversity is a source of strength, creativity, and innovation for UW-Madison. We value the contributions of each person and respect the profound ways their identity, culture, background, experience, status, abilities, and opinion enrich the university community. We commit ourselves to the pursuit of excellence in teaching, research, outreach, and diversity as inextricably linked goals.
The University of Wisconsin-Madison fulfills its public mission by creating a welcoming and inclusive community for people from every background - people who as students, faculty, and staff serve Wisconsin and the world.
The University of Wisconsin-Madison is an Equal Opportunity Employer.
Qualified applicants will receive consideration for employment without regard to, including but not limited to, race, color, religion, sex, sexual orientation, national origin, age, pregnancy, disability, or status as a protected veteran and other bases as defined by federal regulations and UW System policies. We promote excellence by acknowledging skills and expertise from all backgrounds and encourage all qualified individuals to apply. For more information regarding applicant and employee rights and to view federal and state required postings, visit the Human Resources Workplace Poster website.
To request a disability or pregnancy-related accommodation for any step in the hiring process (e.g., application, interview, pre-employment testing, etc.), please contact the Divisional Disability Representative (DDR) in the division you are applying to. Please make your request as soon as possible to help the university respond most effectively to you.
Employment may require a criminal background check. It may also require your references to answer questions regarding misconduct, including sexual violence and sexual harassment.
The University of Wisconsin System will not reveal the identities of applicants who request confidentiality in writing, except that the identity of the successful candidate will be released. See Wis. Stat. sec. 19.36(7).
The Annual Security and Fire Safety Report contains current campus safety and disciplinary policies, crime statistics for the previous 3 calendar years, and on-campus student housing fire safety policies and fire statistics for the previous 3 calendar years. UW-Madison will provide a paper copy upon request; please contact the University of Wisconsin Police Department.