Regulatory Coordinator

Overview

Cancer Care Northwest is hiring a full-time Regulatory Coordinator, responsible for overseeing the regulatory management of phases I-III industry- and federally-sponsored trials as well as investigator-initiated research studies. This includes adherence to rules and regulations concerning the Code of Federal Regulations, Good Clinical Practice and other regulations that govern clinical research studies. This may include preparing, facilitating, coordinating and submitting documentation required by federal, state and local regulations to the central or local IRB to assure the protection of human subjects in research for all CCNW trials.

May assist with monitoring activities along with quality assurance projects.

• Oversee regulatory management of phases I-III industry- and federally-sponsored trials and investigator-initiated research studies.
• Prepare, facilitate, coordinate and submit documentation required by federal, state and local regulations to the central or local IRB.
• Ensure adherence to Code of Federal Regulations, Good Clinical Practice and other regulatory standards to protect human subjects in research.
• Assist with monitoring activities and quality assurance projects as needed.

• Must be detail oriented and able to multi-task to meet standard response times and deadlines.
• Highly motivated with excellent communication, verbal and interpersonal skills; able to demonstrate appropriate conflict resolution in stressful situations.
• Superior customer service skills.
• Ability to work independently and as part of a team.
• Proficient with Microsoft Office.

• Bachelor's degree required or equivalent combination of education and experience.
• Oncology experience preferred.
• Regulatory experience in clinical research preferred.

Benefit information and eligibility can be found at:

Hourly Salary DOE $24.62 - $35.71