Clinical Research Coordinator II - Trials, Data & Compliance

Medical College of Wisconsin; Milwaukee (WI); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Health insurance

403B retirement plan

Paid time off

Tuition reimbursement

Parental leave

Employee assistance program

Life insurance

Job summary

The Medical College of Wisconsin is seeking an administrative professional to support day-to-day operations of clinical research trial programs. You will assist with recruiting, training, supervising staff, and managing the program budget.

Responsibilities include coordinating protocols, enrolling participants, maintaining databases, ensuring regulatory compliance, and preparing IRB documents. You will collaborate across departments and liaise with investigators to keep projects on track.

Qualifications

• Knowledge of biology, chemistry, mathematics, documentation, and records management.
• Data utilization, complex problem solving, critical thinking, resource management, and writing skills.

Responsibilities

• Recruit, screen, enroll and obtain consent from program participants and coordinate training.
• Coordinate research protocols with appointments and procedures, working with other departments and institutions, and maintain participant contact.
• Collect, analyze and disseminate research data; report to investigators; develop and maintain databases and files.
• Identify problems or obstacles in procedures and communicate with investigators.
• Ensure compliance with IRB and regulatory requirements; prepare IRB documents and protocol evaluations.

Skills

Data utilization

Complex problem solving

Critical thinking

Resource management

Writing skills

Biology

Chemistry

Mathematics

Documentation

Records management

Education

Bachelor's degree

Job description

The Medical College of Wisconsin is seeking an administrative professional to support day-to-day operations of clinical research trial programs. You will assist with recruiting, training, supervising staff, and managing the program budget.

Responsibilities include coordinating protocols, enrolling participants, maintaining databases, ensuring regulatory compliance, and preparing IRB documents. You will collaborate across departments and liaise with investigators to keep projects on track.