Clinical Research Project Coordinator III

CHEManager International; Detroit (MI); Presencial; USD 60.000 - 75.000; Jornada completa

Descripción de la vacante

CHEManager International is seeking a Research Project Coordinator in Detroit, MI. Under minimal supervision, you will coordinate studies within CFR guidelines, provide support to Principal Investigators, and interact with internal and external stakeholders at all levels.

You will oversee recruitment, manage day-to-day study operations, and maintain direct contact with potential and enrolled participants. This role may involve handling multiple studies concurrently and ensuring regulatory

Formación

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

Responsabilidades

• Coordinate research projects under minimal supervision within regulatory compliance or CFR guidelines.
• Provide technical support to Principal Investigators and interact with internal and external customers at all levels.
• Oversee recruitment and coordinate day-to-day operations of studies; direct contact with potential and enrolled participants.
• May work on multiple studies simultaneously.

Conocimientos

Study coordination

Regulatory compliance

Recruitment oversight

Stakeholder communication

Educación

Bachelor's degree in a scientific field or related discipline

3 years of relevant experience; 2+ years in research project coordination

Descripción del empleo

CHEManager International is seeking a Research Project Coordinator in Detroit, MI. Under minimal supervision, you will coordinate studies within CFR guidelines, provide support to Principal Investigators, and interact with internal and external stakeholders at all levels.

You will oversee recruitment, manage day-to-day study operations, and maintain direct contact with potential and enrolled participants. This role may involve handling multiple studies concurrently and ensuring regulatory