Research Study Coordinator III Cancer Clinical Translational Research

Henry Ford Health; Detroit (MI); On-site; USD 55,000 - 80,000; Full time

Job summary

Henry Ford Health System's Cancer Clinical and Translational Research Office (CCTRO) is seeking a Research Study Coordinator III to coordinate research projects under regulatory compliance and CFR guidelines.

You will provide technical support to Principal Investigators, oversee recruitment, manage day-to-day study operations, and collaborate with internal and external stakeholders to ensure patient safety and data integrity across multiple studies.

Qualifications

• Bachelor's degree in a scientific field or related area is required.
• Three years of relevant experience with at least two years in research project coordination.

Responsibilities

• Direct contact with potential and enrolled study participants.
• Provide technical support to Principal Investigators.
• Coordinate day-to-day operations of the study and recruitment oversight.
• Interact with internal and external customers at all levels.

Skills

Recruitment coordination

Clinical research support

Education

Bachelor's degree in scientific field

SOCRA or ACRP and IATA certification

Job description

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.

Qualifications:

Qualifications

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.