Hybrid Oncology Clinical Research Coordinator

Virginia Commonwealth University; Richmond (VA); Hybrid; USD 47,000 - 57,000; Full time

Job summary

Virginia Commonwealth University is seeking a Clinical Research Coordinator to support Principal Investigators in activation, execution, and management of oncology clinical trials. The role involves patient recruitment, data collection, and adherence to IRB requirements within a hybrid work setting.

Ideal candidates have a Bachelor’s degree in health research or related fields, at least 1 year of relevant experience, and certification readiness in GCP/IRB processes.

Qualifications

• Bachelor’s degree in health research and/or healthcare-related fields or equivalent combination of education, experience, and training.
• At least 1 year of relevant experience.
• Must be able to complete mandatory competencies and certifications required by VCU and VCU Health, individual clinical trials and the NIH Human Subjects Protection training.

Responsibilities

• Responsible for participant recruitment, enrollment, tracking, data collection, and verification of data in the study database.
• Maintain understanding of clinical research management duties from study initiation to closeout.
• Maintain current CITI credentials for Human Subjects Protections, Good Clinical Practice (GCP), and additional certifications as required.
• Understand and adhere to all IRB requirements, Human Subjects protection regulations, and all aspects of IRB approved protocols.
• Engage in various forms of communication about the studies they are assisting.
• Be directly responsible for study coordination of an assigned portfolio of oncology clinical research studies covering a variety of diseases and conditions.

Education

Bachelor’s degree in health research and/or healthcare-related fields

Job description

Virginia Commonwealth University is seeking a Clinical Research Coordinator to support Principal Investigators in activation, execution, and management of oncology clinical trials. The role involves patient recruitment, data collection, and adherence to IRB requirements within a hybrid work setting.

Ideal candidates have a Bachelor’s degree in health research or related fields, at least 1 year of relevant experience, and certification readiness in GCP/IRB processes.