Medicine Clinical Research Coordinator II - Impact

Milwaukee Succeeds; Milwaukee (WI); Sur place; USD 65 000 - 90 000; Plein temps

Avantages offerts par ce poste

Health insurance

Vision and dental

403B retirement plan

Vacation and paid holidays

Tuition reimbursement

Parental leave

EFAP

Pet insurance

Onsite fitness facility

Discounts

Résumé du poste

The Medical College of Wisconsin (MCW) is seeking a Clinical Research Coordinator II to manage day-to-day administrative activities of clinical research trial programs, support team goals, and assist with staffing and budgeting.

Responsibilities include recruiting and consenting participants, coordinating protocols and visits, maintaining databases, ensuring IRB compliance, and collaborating on program materials and outreach.

Qualifications

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

Responsabilités

• Recruit, screen, enroll and obtain consent from program participants.
• Coordinate research protocols including appointments and procedures; liaise with other departments.
• Collect, analyze, and disseminate research data; maintain databases and files.
• Identify problems or obstacles; communicate with investigators.
• Ensure compliance with IRB and regulatory requirements.
• Prepare IRB documents and write protocols with investigators.
• Develop program materials including educational, marketing materials, websites, forms, and reports.
• Maintain program timeline and deadlines.
• Coordinate outreach activities with community organizations; organize meetings and events.
• Monitor study budgets; assist with funding opportunities.

Connaissances

Biology

Chemistry

Mathematics

Documentation

Records management

Data utilization

Problem solving

Critical thinking

Resource management

Writing

Formation

Bachelor's degree

Outils

CITI training

Description du poste

The Medical College of Wisconsin (MCW) is seeking a Clinical Research Coordinator II to manage day-to-day administrative activities of clinical research trial programs, support team goals, and assist with staffing and budgeting.

Responsibilities include recruiting and consenting participants, coordinating protocols and visits, maintaining databases, ensuring IRB compliance, and collaborating on program materials and outreach.