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

CHEManager International; Detroit (MI); Vor Ort; USD 55.000 - 75.000; Vollzeit

Zusammenfassung

Henry Ford Health System seeks a Research Study Coordinator III to oversee multiple cancer research projects under CFR guidelines. You will provide technical support to principal investigators and coordinate day-to-day study activities, including participant recruitment and interactions with internal and external stakeholders.

The role requires a Bachelor's degree in a scientific field and 3+ years of relevant experience, with at least 2 years in study coordination; SOCRA/ACRP and IATA

Qualifikationen

• Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related field.
• Minimum 3 years of relevant experience with at least 2 years of research project coordination experience.
• SOCRA or ACRP and IATA certification required.

Aufgaben

• Coordinate research projects under regulatory guidelines and CFR.
• Provide technical support to Principal Investigators and recruit participants.
• Interact with internal and external stakeholders and manage day-to-day study operations.

Kenntnisse

Clinical coordination

Regulatory coordination

Data management

Ausbildung

Bachelor's degree in scientific field

Jobbeschreibung

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.