Clinical Research Coordinator jobs in Wisconsin

Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)

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Research Coordinator
  • Circuit Clinical
  • Madison, WI FULL_TIME
  • Description

    Circuit Clinical® is on a mission to transform the way people find, choose, and participate in clinical research.


    We are searching for a Research Coordinator to join our team! 


    Circuit Clinical was ranked 20th nationally for Best Workplaces for Innovators by Fast Company® and was named an Inc. Magazine® Best Workplaces 2021. Topping a long list of innovation and startup awards over the last 5 years – including winning SCOPE’s Participant Engagement Award and winning at 43North - Circuit recently won Fast Company’s World Changing Ideas™ Award. 


    Our award-winning culture is grounded on a belief in the values of transparency, inclusion, accountability, performance, talent seeking, & continuous learning.  We live these values every day and we’re looking for a leader who embodies them. Our focus is on building an incredible, hard charging Team and on providing them with the opportunity to do the best work of their careers. In short, we’re motivated to take on the hardest problems in the development of new medicines – this is Work That Matters. 


    To accomplish our Mission, we know we must recruit the most dynamic, mission-driven, empathetic, and passionate leaders in our industry. That’s where you come in! 


    What We Offer: 

    If you’ve been looking for a chance to work with an amazing, highly motivated team and to have direct impact in building a transformative clinical trials company every day – that is exactly what we’re offering. We provide competitive benefits and an environment focused on helping you grow personally and professionally.  


    What You Will Bring to Circuit Clinical: 

    As our Research Coordinator, you will be responsible for coordinating, facilitating, and monitoring the implementation of research study protocols being conducted in accordance with departmental policy, institutional policy, sponsor requirements, and FDA regulations. You will also provide, manage, and coordinate care for patients participating in clinical trials in compliance with written study protocols. 

    Requirements

    You’ll Be Responsible For: 

    • Having thorough knowledge of study protocol, including inclusion and exclusion criteria and confirmation of subject eligibility 
    • Knowledge of study endpoints, reportable events (Adverse Event, Serious Adverse Event, Adverse Events of Special Interest) 
    • Knowledge of disease process and standard of care 
    • Completion of study screen tool and study summary 
    • Defining methods of subject identification and recruitment 
    • Thorough knowledge of protocol to conduct Informed Consent Form process 
    • Completion of screening procedures, randomization, and subject visits 
    • Investigational Product dispensing and accountability 
    • Scheduling of study visits in compliance with protocol(s) 
    • Preparation and maintenance of source documents and IRB submitted documents for recruitment 
    • Assisting in recruitment efforts, contacting and identifying potentially eligible participants to screen 
    • Confirming Primary Investigator review of study visits 
    • Reviewing Adverse Events and Serious Adverse Event with Primary Investigator within 24 hour of event report to Institutional Review Board (IRB) and sponsor 
    • Subject retention activities and follow up procedures 
    • Obtaining consents for amendments where applicable 
    • Participating in protocol amendment training and updates essential documents accordingly 
    • Sponsoring monitoring activities, preparation, data clarification 
    • Weekly review of study status 
    • Obtaining appropriate certification of required trainings 
    • Contributing to patient recruitment efforts as business demands require. 

    Your Qualifications: 

    • Bachelor’s degree required.? 
    • Minimum 3 years experience as a Research Coordinator; or one year of RN level nursing, direct patient care in hospital setting or clinical research nurse 

    Your Preferred Experience: 

    • Licensed as a registered nurse (RN) in the state of Wisonsin, preferred. 
    • Certification of Clinical Research Coordinator, preferred. If no certification, willing to obtain certification within two years. 
    • Computer literacy including Microsoft office (Word, Excel), Google suite, and CTMS software a plus. 

    Who You Are: 

    We prize 4 traits above all others: 

    Hungry: we like people who are ambitious for themselves AND for our Mission and for each other – we’ll all win together and that takes real drive 

    Happy: we seek pragmatic optimists – pessimism and ironic dispositions, especially in leadership can kill startups – we seek those who know the world can be improved by those who work hard and smart to change it 

    Humble: not the false “I’m not really anything” kind of modesty – we like swagger! But we prize people who are confident who know they are great, and so is everyone around them… and act accordingly 

    Smart: there are a LOT of smart people here… but smart is last for a reason. We want those kinds of smart people who can collaborate and respect the intelligence of others. 


    What Else Predicts Success and Happiness for you at Circuit? 

    • Your organizational skills are top notch. You will need to be comfortable handling a great deal of information from various sources including internal and external. 
    • Your accuracy and attention to detail are among your best qualities - you enjoy the fine print. This is a critical skill in this role. 
    • You prioritize and focus well. You may be coordinating several studies in tandem and this will require prioritization and focus. 
    • You enjoy learning about new disease states and are able to understand medical jargon as well as explain in layman's terms to your study participants. 
    • You enjoy learning new systems and technology. 
    • You are able take direction from the Principal Investigator, superiors, and teammates. 
    • You are able to identify problems and escalate issues quickly. 
    • You have a patient first mentality. 
    • You have a way of putting the study participants at ease, addressing their concerns in a calm and warm manner.
       

    The Other Fine Print: 

    Location: This position is located at our Madison, WI clinical site.

    Travel: May require regular travel to other research site locations. 

    Exemption Status: Full time, exempt. 

    Physical Requirements: the following physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions:  

    Regularly required to stand; walk; use hands; reach with hands and arms; stoop, kneel, crouch, or crawl and talk or hear.  

    Occasionally required to sit. Occasionally lift and/or move up to 50 pounds. Specific vision abilities include close vision, distance vision, peripheral vision, depth perception and ability to adjust focus. 

    Other Duties: the duties and responsibilities described are not a comprehensive list and that additional tasks may be assigned to the employee from time to time; or. the scope of the job may change as necessitated by business demands. 

  • 16 Days Ago

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Operations Coordinator I
  • CRU Fortrea Clinical Research Unit Inc.
  • Madison, WI FULL_TIME
  • As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical...
  • 12 Days Ago

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Lab Coordinator (on-site Madison, WI)
  • CRU Fortrea Clinical Research Unit Inc.
  • , WI FULL_TIME
  • As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical...
  • 19 Days Ago

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Clinical Research Coordinator
  • Mercyhealth
  • Janesville, WI FULL_TIME
  • Overview The primary function of the Clinical Research Coordinator (CRC) is to coordinate the conduct of clinical research studies in a clinic/hospital setting with an emphasis on the screening, enrol...
  • 19 Days Ago

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Clinical Research Coordinator
  • Mercy Health Corporation
  • Janesville, WI FULL_TIME
  • OverviewThe primary function of the Clinical Research Coordinator (CRC) is to coordinate the conduct of clinical research studies in a clinic/hospital setting with an emphasis on the screening, enroll...
  • 21 Days Ago

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Clinical Research Coordinator- Biobank
  • Versiti, Inc.
  • Wauwatosa, WI FULL_TIME
  • Overview Versiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute...
  • 23 Days Ago

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Clinical Research Coordinator
  • ObjectiveHealth
  • Woodway, TX
  • Clinical Research Coordinator Our clinical research company is looking to hire a qualified candidate for the full-time p...
  • 3/29/2024 12:00:00 AM

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Clinical Research Coordinator
  • Northwest Georgia Oncology Centers, PC
  • Hiram, GA
  • Job Description Job Description Busy oncology practice has an immediate opening for a FT Clinical Research Coordinator. ...
  • 3/29/2024 12:00:00 AM

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Clinical Research Coordinator
  • NYU Langone Health
  • New York, NY
  • NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Sanford Health
  • Fargo, ND
  • Create Your Career With Us! Sanford Health is one of the largest and fastest-growing not-for-profit health systems in th...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Apex Systems
  • Burlingame, CA
  • Apex Systems is seeking a Clinical Research Coordinator to support data collection in the lab. This role will work with ...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Danbury Health Systems
  • Poughkeepsie, NY
  • Full Time Clinical Research Coordinator Opportunity - Poughkeepsie, NY (75 Miles from New York City) Nuvance Health has ...
  • 3/28/2024 12:00:00 AM

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Clinical Research Coordinator
  • Beth Israel Lahey Health
  • Boston, MA
  • When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives. Job Typ...
  • 3/27/2024 12:00:00 AM

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Clinical Research Coordinator
  • CARLE
  • Peoria, IL
  • Promotes good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federa...
  • 3/26/2024 12:00:00 AM

Wisconsin is bordered by the Montreal River; Lake Superior and Michigan to the north; by Lake Michigan to the east; by Illinois to the south; and by Iowa to the southwest and Minnesota to the northwest. A border dispute with Michigan was settled by two cases, both Wisconsin v. Michigan, in 1934 and 1935. The state's boundaries include the Mississippi River and St. Croix River in the west, and the Menominee River in the northeast. With its location between the Great Lakes and the Mississippi River, Wisconsin is home to a wide variety of geographical features. The state is divided into five dist...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$59,183 to $79,787

Clinical Research Coordinator in Rock Hill, SC
A clinical research coordinator coordinates the clinical trials under the guidance of the principal investigator.
October 22, 2019
Clinical Research Coordinator in Binghamton, NY
However, many people start working in research with no experience and can receive on-the-job training and experience.
November 18, 2019
Clinical Research Coordinator in Portsmouth, NH
With an experienced coordinator, just as with an inexperienced one, it’s the same.
December 11, 2019