Clinical Trials Coordinator II — Impactful Onsite Research

University of Wisconsin–Madison; Madison (WI); On-site; USD 50,000 - 55,000; Full time

Benefits offered by this job

Sick time

Job summary

The University of Wisconsin–Madison, Department of Medicine, Office of Research Services, is hiring multiple Clinical Research Coordinators to support a portfolio of clinical trials across subspecialties. CRC I and CRC II levels will handle tasks from simple studies to more complex trials under supervision, reporting to the DOM Clinical Trial Research Supervisor.

Ideal candidates will demonstrate strong attention to detail, time management, and the ability to work with patients and researchers,

Qualifications

• Reading and understanding research principles and methodology and applying that knowledge in a clinical trials environment.
• Strong oral and written communication skills.
• Ability to interact with patients and researchers independently using initiative and good judgment.
• Ability to structure time to meet multiple deadlines.

Responsibilities

• Serves as an initial point of contact for clinical research participants and staff, informing on procedures and study expectations.
• Recruits, screens, determines eligibility, and enrolls trial participants under supervision of a licensed professional.
• Manages research workflow components, collects, prepares, processes, and submits participant data and samples per protocols.
• Identifies resource needs and manages supply and equipment inventory for trials.
• Schedules logistics, determines workflows, and secures resources for defined trials.

Skills

Research principles

Communication skills

Interpersonal skills

Time management

Education

Bachelor’s Degree preferred

Job description

The University of Wisconsin–Madison, Department of Medicine, Office of Research Services, is hiring multiple Clinical Research Coordinators to support a portfolio of clinical trials across subspecialties. CRC I and CRC II levels will handle tasks from simple studies to more complex trials under supervision, reporting to the DOM Clinical Trial Research Supervisor.

Ideal candidates will demonstrate strong attention to detail, time management, and the ability to work with patients and researchers,