Hybrid Clinical Research Coordinator I

Corewell Health; Grand Rapids (MI); Hybrid; USD 60,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits package

On-demand pay

Discounts directory

Identity theft protection

Retirement options

Job summary

Corewell Health in Grand Rapids is seeking a Research Coordinator to support principal investigators in designing, evaluating, and implementing clinical studies that advance practice. With a focus on feasibility, budgeting, IRB documents, data collection, and regulatory compliance, you will coordinate subject recruitment, enrollments, and study activities across multiple sites and teams.

This full-time role follows a daytime schedule with a hybrid on-site requirement in Grand Rapids, aligning

Qualifications

• Bachelor's degree in health or science related field or equivalent.
• 1 year of relevant experience in clinical research and project management.
• CRT-BLS - ARC or CRT-BLS - AHA, 90 days required.

Responsibilities

• May serve as primary coordinator / project manager on a variety of research studies with low or moderate regulatory, clinical, and operational complexity; supports the PI and research team members.
• Evaluates and prepares research studies for implementation including: assessment of operational feasibility; budget development; preparation of IRB documents; institutes protocol operations (data collection tools, case report forms); attends study meetings.
• Identifies, recruits, screens, and enrolls eligible subjects per protocol; with appropriate training and delegation, performs protocol-required research activities and/or protocol-required research procedures with low clinical complexity (e.g. six-minute walk test, SF-36, etc.).
• Monitors patient status; collects, reviews, and documents data into a variety of systems per protocol.
• Maintains research studies in compliance with federal, state, and local law, GCP, contracts, and institutional policies.
• Coordinates and/or performs study activities which may include: identification of adverse events; assist with management of investigational product/test article; collection, processing, and shipment of research specimens; and other research activities to the extent permitted by law and policy.
• Communicates, collaborates, networks, and acts as a consultant to the study sponsor and/or CRO, research study centers, academic institutions, investigators, physicians/physician offices, ancillary departments, and the multidisciplinary team (including students and residents).

Skills

Clinical research

Project management

Education

Bachelor's degree in health or science related field

Job description

Corewell Health in Grand Rapids is seeking a Research Coordinator to support principal investigators in designing, evaluating, and implementing clinical studies that advance practice. With a focus on feasibility, budgeting, IRB documents, data collection, and regulatory compliance, you will coordinate subject recruitment, enrollments, and study activities across multiple sites and teams.

This full-time role follows a daytime schedule with a hybrid on-site requirement in Grand Rapids, aligning