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University of Wisconsin–Madison
Madison, WI | Full Time
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University of Wisconsin–Madison
Madison, WI | Full Time
$56k-73k (estimate)
4 Months Ago
Clinical Research Coordinator II
$56k-73k (estimate)
Full Time 4 Months Ago
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University of Wisconsin–Madison is Hiring a Clinical Research Coordinator II Near Madison, WI

Job Summary:

UW Clinical Trials Institute (CTI) is a partnership between the University of Wisconsin School of Medicine and Public Health (SMPH) and UW Health. It supports clinical research professionals, investigators, and participants to advance discovery and research in the prevention, detection, and treatment of disease to help improve the health of individuals, families, and communities across Wisconsin and beyond. Our exceptionally talented workforce provides care, support, and provide information to clinical trials participants; resources, training, and guidance to research professionals; and opportunities for industry partners to advance groundbreaking medical research.
The CTI has an exciting opportunity for an 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, flexibility is essential, as occasional early mornings, evenings, or weekends may be required to accommodate the schedules of the research participants. Additionally, the role may involve travel between research sites within the metro Madison area. If you are ready to make a meaningful impact in the field of clinical research, we encourage you to apply today!
At CTI we consider diversity broadly, understanding each person's life and community experiences makes them unique. We believe diverse abilities/disabilities, racial/ethnic and cultural backgrounds, age, genders and gender identities and expressions, educational experiences and life stories drive true innovation and an exceptional work environment.

Responsibilities:Coordinates clinical research studies, performing a variety of tasks and activities. Recruits, screens, selects, determines eligibility, and enrolls study participants and ensures subjects follow the research protocol. Develops study-related documents. Applies expertise, knowledge, and skills to a broad range of different types of clinical studies, navigates resources, and identifies issues needing escalation. Contributes to development of new team and unit processes, procedures, staff, and tools.
  • 10% Schedules logistics, determines workflows, and secures resources for clinical research trials
  • 15% Recruits, screens, selects, determines eligibility and enrolls trial participants, collects more complex information, performs medical assessments, and answers varied questions under supervision of a medically licensed professional. Performs medical assessments after completion of required training/certification, such as collecting vital signs, obtaining weight, and performing phlebotomy
  • 15% Manages research workflow components, collects, prepares, processes, and submits participant data and samples to appropriate entities, adhering to research protocols
  • 10% Identifies work unit resources needs and manages supply and equipment inventory levels
  • 10% Serves as a main point of contact for clinical research participants, providing information regarding research procedures, expectations, and informational inquiries. Ensures participants follow the research protocol and alerts Principal Investigator of issues
  • 5% Performs quality checks
  • 10% Identifies resource needs and develops clinical research documents, such as job aids, tools, processes, procedures, and training. Contributes to the development of protocols
  • 5% May assist with training of staff
  • 10% Reconcile research billing, payments, and invoices and financial issues in concert with CTI financial specialists
  • 10% Participate in quality and process improvement endeavors within the CTI; contribute to the development of new workflows and demonstrate flexibility in an evolving environment.
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.
For more information on diversity and inclusion on campus, please visit: Diversity and Inclusion

Education:

Preferred
Bachelor's Degree

Qualifications:

Required:

- At least 2 years of prior clinical research coordination experience.

Preferred:

- Health or science related college degree or equivalent education and experience.
- Previous experience with basic clinical assessments including phlebotomy.
- Previous experience with research applications used in the UW CTI: OnCore, eBinders (Florence), Advarra Payments, EPIC, etc.
- Experience with training new staff.

Work Type:

Full Time: 100%
It is anticipated this position requires work be performed in-person, onsite, at a designated campus work location.

Appointment Type, Duration:

Ongoing/Renewable

Salary:

Minimum $50,000 ANNUAL (12 months)
Depending on Qualifications

Additional Information:

Required:
- Ability to work with minimal supervision with diverse teams of physicians, coordinators, collaborators, and study sponsors in a diplomatic, collaborative, and effective manner.
- Ability to effectively multi-task, work well under time multiple time constraints, and meet competing deadlines.
- Excellent interpersonal, oral, and written communication skills
- Self-motivated, exceptional attention to detail, and able to exercise good judgement.
- Understanding of medical terminology.
- Strong organizational skills including the use of Microsoft applications (word, excel, etc.)
- Able to quickly problem solve and resolve conflict.
- Travel to multiple sites required, must have reliable transportation.
- Valid Driver's License
- Current ACRP or SoCRA Certification or ability to become certified within 6 months of hire.
The selected applicant will be responsible for ensuring eligibility for employment in the United States on or before the effective date of the appointment. University sponsorship is not available for this position
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.

How to Apply:

To apply for this position, please click on the "Apply Now" button. You will be asked to upload a current resume/CV and a cover letter briefly describing your qualifications and experience. You will also be asked to provide contact information for three (3) references, including your current/most recent supervisor during the application process. References will not be contacted without prior notice.

Contact:

Jennifer Wilkie
jwilkie@wisc.edu
608-262-8025
Relay Access (WTRS): 7-1-1. See RELAY_SERVICE for further information.

Official Title:

Clin Res Coord II(RE016)

Department(s):

A53-MEDICAL SCHOOL/CLINICAL RESEARCH

Employment Class:

Academic Staff-Renewable

Job Number:

299344-AS

The University of Wisconsin-Madison is an Equal Opportunity and Affirmative Action Employer.Qualified applicants will receive consideration for employment without regard to, including but not limited to, race, color, religion, sex, sexual orientation, gender identity, 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 through diversity and encourage all qualified individuals to apply.
If you need to request an accommodation because of a disability, you can find information about how to make a request at the following website: https://employeedisabilities.wisc.edu/disability-accommodation-information-for-applicants/
Employment may require a criminal background check. It may also require you and your references to answer questions regarding 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.

Job Summary

JOB TYPE

Full Time

SALARY

$56k-73k (estimate)

POST DATE

02/05/2024

EXPIRATION DATE

06/27/2024

The job skills required for Clinical Research Coordinator II include Clinical Research, Clinical Trial, Initiative, Data Collection, Planning, Scheduling, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Coordinator II. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Coordinator II. Select any job title you are interested in and start to search job requirements.

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