Research Specialist I — Study Coordination & Data

University of Missouri System; New York (NY); Presencial; USD 24 000 - 25 000; Tempo integral

Resumo da oferta

The University of Missouri System’s Department of Physical Medicine & Rehab is seeking a Research Specialist I to recruit participants for studies, assist with data collection, and coordinate study visits. You will manage regulatory documents and support daily program activities using established procedures.

The role involves IRB-related tasks, consent processes, and data entry, with a standard Monday–Friday schedule. Prior experience in clinical research is valued.

Qualificações

• Bachelor's degree or equivalent combination of education and relevant experience.
• At least 1 year of experience from which comparable knowledge and skills can be acquired.

Responsabilidades

• Recruit participants for research studies (including screening and consenting).
• Assisting/performing clinical/behavioral data collection acquisition and imputing the data.
• Coordinate, mange, and schedule research study visits; manage devices mailing to participants.
• Complete annual IRB reviews, submit amendments, and maintain regulatory documents for research studies.
• Program support for daily activities as assigned using existing procedures.

Conhecimentos

Clinical coordination

Data collection

Formação académica

Bachelor's degree or equivalent

Descrição da oferta de emprego

The University of Missouri System’s Department of Physical Medicine & Rehab is seeking a Research Specialist I to recruit participants for studies, assist with data collection, and coordinate study visits. You will manage regulatory documents and support daily program activities using established procedures.

The role involves IRB-related tasks, consent processes, and data entry, with a standard Monday–Friday schedule. Prior experience in clinical research is valued.