Senior Clinical Research Coordinator: Trials & Compliance

Medical College of Wisconsin; Milwaukee (WI); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Health insurance

Vision and dental coverage

Flexible spending options

403B retirement plan

Vacation and paid holidays

Tuition reimbursement

Parental leave

Employee assistance program

Pet insurance

On-campus fitness facility

Job summary

The Medical College of Wisconsin is seeking a Program Administrator to coordinate the day-to-day administrative activities of the clinical research trials program. You will support the team to achieve program goals, recruit, train, and supervise staff, and manage study budgets.

Responsibilities include overseeing participant recruitment and consent, coordinating protocols with departments and institutions, and ensuring regulatory compliance.

Qualifications

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

Responsibilities

• Coordinate day-to-day administrative activities of the clinical research trials program.
• Recruit, train, and supervise staff; manage study budgets.
• Oversee recruitment, screening, enrollment, and consent of participants; coordinate trainings.
• Coordinate research protocols with other departments and institutions; maintain contact with participants.
• Oversee data collection, analysis, and dissemination; develop and maintain databases and files.

Skills

Biology knowledge

Data management

Regulatory compliance

Staff supervision

Budget management

Education

Bachelor’s Degree

Job description

The Medical College of Wisconsin is seeking a Program Administrator to coordinate the day-to-day administrative activities of the clinical research trials program. You will support the team to achieve program goals, recruit, train, and supervise staff, and manage study budgets.

Responsibilities include overseeing participant recruitment and consent, coordinating protocols with departments and institutions, and ensuring regulatory compliance.