Clinical Research Coordinator II — Impactful Trials & Data

Medical College of Wisconsin

Wauwatosa (WI)

On-site

USD 48,000 - 70,000

Full time

8 days ago

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Benefits offered by this job

Health insurance
Dental coverage
Paid time off

Job summary

The Medical College of Wisconsin is seeking a Program Administrative Specialist to support day-to-day activities of the clinical research trials program. You will recruit, screen, enroll, and obtain consent from participants across clinics within Froedtert Health and community settings, coordinating training and maintaining engagement with study participants.

You will assist in protocol coordination, data collection and reporting, and ensuring IRB compliance.

Qualifications

  • Bachelor's degree required.
  • Minimum 2 years of experience.
  • CITI training within 90 days of hire.

Responsibilities

  • Recruit, screen, enroll and obtain consent from program participants across primary care and specialty clinics; coordinate training for participants.
  • Coordinate research protocols including arranging appointments and procedures, collaborating with departments, and maintaining contact with study participants.
  • Collect, analyze, and disseminate program data; report progress to stakeholders.
  • Identify problems or obstacles in the system related to protocol implementation and communicate with investigators.
  • Ensure compliance with IRB and regulatory requirements.

Skills

Biology
Chemistry
Mathematics
Documentation
Records management
Data utilization
Problem solving
Critical thinking
Resource management
Writing skills

Education

Bachelor's degree

Job description

The Medical College of Wisconsin is seeking a Program Administrative Specialist to support day-to-day activities of the clinical research trials program. You will recruit, screen, enroll, and obtain consent from participants across clinics within Froedtert Health and community settings, coordinating training and maintaining engagement with study participants.

You will assist in protocol coordination, data collection and reporting, and ensuring IRB compliance.

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