Research Study Coordinator III - Cancer Clinical & Translational Research - 40 hours - Days

CHEManager International; Detroit (MI); On-site; USD 55,000 - 75,000; Full time

Job summary

Henry Ford Health System is seeking a Research Study Coordinator III to manage and coordinate cancer-focused clinical trials under regulatory guidelines. The role involves direct interaction with participants, coordination with investigators, and overseeing study operations to ensure high-quality care for patients and efficient trial progress.

The position requires a Bachelor's degree in a scientific field, 3 years of relevant experience (2+ in coordination), and SOCRA/ACRP and IATA

Qualifications

• Bachelor's degree in a scientific field is required.
• Three years of relevant experience with at least two years in research project coordination.
• SOCRA or ACRP and IATA certification required.

Responsibilities

• Direct contact with potential and enrolled study participants; provide support as required.
• May work on multiple studies simultaneously; oversee recruitment and day-to-day study operations.
• Provide technical support to Principal Investigators and ensure regulatory compliance.

Skills

Communication

Coordination

Regulatory awareness

Education

Bachelor's degree in a scientific field

Job description

The Cancer Clinical and Translational Research Office (CCTRO) is the largest clinical research department at Henry Ford Health System. We manage approximately 200 ongoing trials that focus on the prevention, diagnosis, treatment and cure of cancer. Our staff have highly specialized roles in clinical coordination, research nursing, data management, regulatory coordination, grant management, and research sample processing. This is a fast growing program that is working with the Henry Ford Health and Michigan State University Health Sciences Partnership toward National Cancer Institute designation. The CCTRO is very team driven and passionate about providing high quality care to our patients and excellent support to our physician investigators.

General Summary

Under minimal supervision, the Research Study Coordinator III is responsible for coordinating research projects within guides of regulatory compliance and/or Code of Federal Regulation.

• Provides technical support to Principal Investigators.
• Duties include but not limited to, interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study.

Duties Include But Not Limited To

• Direct contact with potential and enrolled study participants expected. Provides other support as required.
• May work on multiple studies at any given time.

Education Required

• Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related field.

Experience Required

• Three (3) years of relevant experience with at least two (2) years of research project coordination experience.

Certifications/Licensures Required

• SOCRA or ACRP and IATA certification required.