Clinical Research Coordinator I: Trials, Data & Compliance

The Medical College of Wisconsin, Inc.

Wauwatosa (WI)

On-site

USD 55,000 - 75,000

Full time

3 days ago
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Benefits offered by this job

Health insurance
403B Retirement Package
Paid Parental Leave
Tuition Reimbursement

Job summary

The Medical College of Wisconsin, Inc. (MCW) is hiring for an administrative professional to support the clinical research trials program in Wisconsin.

The role involves recruiting and consenting participants, coordinating training and study procedures, and ensuring regulatory compliance within a collaborative environment. You will collect and analyze program data, prepare reports, and assist investigators in developing study protocols and materials.

Qualifications

  • Associate's Degree required; equivalent experience considered.
  • At least 1 year of relevant experience.
  • CITI training within 90 days of hire.
  • Ability to maintain accurate documentation and records.

Responsibilities

  • Recruit, screen, enroll and obtain consent from program participants.
  • Coordinate training for program participants.
  • Coordinate research protocols and appointments with departments and institutions.
  • Collect, analyze, and disseminate program data.
  • Ensure compliance with IRB and regulatory requirements.
  • Assist in IRB document preparation and protocol writing.
  • Develop program materials and manage databases and files.
  • Maintain program timeline and track deadlines.

Skills

Recruitment coordination
Data analysis
Documentation
Report writing

Education

Associate's Degree
Equivalent experience considered

Tools

CITI training

Job description

The Medical College of Wisconsin, Inc. (MCW) is hiring for an administrative professional to support the clinical research trials program in Wisconsin.

The role involves recruiting and consenting participants, coordinating training and study procedures, and ensuring regulatory compliance within a collaborative environment. You will collect and analyze program data, prepare reports, and assist investigators in developing study protocols and materials.

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