Full-Time

Clinical Research Coordinator 2

Paulsen Lab

Posted on 5/12/2026

Deadline 5/22/26
University of Wisconsin-Madison

University of Wisconsin-Madison

Compensation Overview

$50k/yr

No H1B Sponsorship

Madison, WI, USA

Hybrid

Hybrid work: some remote/offsite work may be possible; in-person on Madison, WI campus required.

Category
Biology & Biotech (1)
Required Skills
Inventory Management
Ruby
Google Cloud Platform
Requirements
  • At least 3 years of experience in Human Subjects research with direct participant interaction
  • Must show career progression in this or similar field
  • Experience with collecting, processing, handling, or shipping biological samples
  • Ability to communicate effectively in English, both verbally and in writing, as required to conduct cognitive testing and obtain informed consent
Responsibilities
  • Identifies resource needs and develops clinical research documents, such as job aids, tools, processes, procedures, and training. Contributes to the development of protocols
  • Identifies work unit resources needs and manages supply and equipment inventory levels
  • Supervise lab undergraduate students
  • 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
  • May assist with training of staff
  • Oversee biospecimen processing lab
  • Participate in community-based events to introduce research programs and disseminate project information to the general public
  • Manages research workflow components, collects, prepares, processes, and submits participant data and samples to appropriate entities, adhering to research protocols
  • 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
  • Presentation and collection of informed consent to implement all ethical principles of good clinical research practices. May submit and maintain appropriate IRB submissions
  • Schedules logistics, determines workflows, and secures resources for clinical research trials
  • Performs quality checks
Desired Qualifications
  • Previous supervisory experience
  • Previous UW-Madison experience
  • Previous experience with IRB submissions
  • Previous experience writing standard operating procedures
  • Previous experience with administration of Neuropsych exam testing
  • Bachelor’s Degree preferred; focus in Psychology, Biology or related field preferred
University of Wisconsin-Madison

University of Wisconsin-Madison

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