Clinical Research Analyst – Tumor Institute

Role Overview

• Prepares, facilitates, coordinates, and submits documentation required by federal, state and local regulations and institutional requirements relating to the conduct of research.
• This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA‑required submissions which may include investigator 1572 forms, investigational new drug applications, device submissions such as Emergency use, HDE, Safety Reports, and other documents that may be required by a regulatory agency or the institution.
• Leads the work of Research Assistants on a task-basis if applicable.
• Provides on-the-job training, sets priorities and schedules workflow required to support project objectives.

Requirements

• Bachelor's Degree Preferably in science, healthcare, or other related field --or-
• Significant experience in research coordination or regulatory work may be substituted for educational requirements
• 2 years of experience in healthcare, research or clinical setting with regulatory compliance familiarity

Benefits

• Health care benefits (medical, dental, vision)
• 401(k) Savings Plan with employer matching
• Life insurance
• Disability insurance
• Paid time off benefits (paid parental leave, vacations, holidays, health issues)
• Voluntary benefits
• Well-being resources