University of Wisconsin-Madison je javna raziskovalna univerza v Madisonu v zvezni državi Wisconsin ter vodilni kampus sistema University of Wisconsin. Njena akademska in raziskovalna skupnost zajema humanistiko, naravoslovje in uporabne discipline, pri čemer se v raziskave vsako leto vloži več kot milijarda dolarjev. Univerza povezuje dodiplomsko in podiplomsko izobraževanje z delom v skupnosti, viri kampusa in športom ter se pri tem ravna po usmeritvi Wisconsin Idea, ki poudarja služenje javnosti. Pri svojem delovanju poudarja tudi raznolikost, vključujočo odličnost in sodelovanje s širšo skupnostjo.
Clinical Research Coordinator, Women’s Health — UW–Madison
Coordinate women’s health clinical research at UW–Madison, supporting maternal and fetal medicine and obstetrics and gynecology studies. Responsibilities include participant recruitment, data and sample handling, and multi-center study coordination.
Opis
- Support maternal and fetal medicine and obstetrics and gynecology research within the Human Subjects Core.
- Collaborate with faculty researchers on women’s health studies.
- Coordinate clinical studies funded internally and externally, including multi-center collaborations.
- Manage research workflows and collect, prepare, process, and submit participant data and samples in line with study protocols.
- Recruit, screen, assess eligibility for, select, and enroll trial participants.
- Collect participant information and answer questions under the supervision of a licensed medical professional.
- After required training or certification, conduct basic assessments such as taking vital signs, measuring weight, and performing phlebotomy.
- Act as an initial contact for research participants and clinical staff.
- Explain study procedures and expectations, and answer informational questions.
- Monitor participants’ adherence to study protocols and raise concerns with the Principal Investigator.
- Coordinate trial logistics, set workflows, and arrange required resources.
- Identify work unit resource needs and maintain supply and equipment inventory.
Zahteve
- Previous experience in a research setting.
- Familiarity with clinical trial processes and management.
- Proficiency with data management and clinical trial software.
- Must pass an initial caregiver check and repeat checks every four years under Wisconsin Caregiver Law.
- Experience with human subjects research is preferred.
- Data entry experience is preferred.
- Experience with electronic data capture (EDC) systems is preferred.
- Schedule flexibility is preferred.
- A Bachelor of Science degree is preferred.
- A cover letter is required.
- A resume is required.
- Must remain eligible to work in the United States without employer sponsorship.
- The university does not provide sponsorship, including sponsorship transfers or TN visas.
- Employment may be subject to a criminal background check.
- Final candidates will be asked to provide references.
Ugodnosti
- Generous vacation, holiday, and sick leave.
- Competitive insurance plans and savings accounts.
- Retirement benefits.
- Mentorship from faculty researchers.
- Professional networking through multi-center research collaborations.