Clinical Research Analyst — IRB/FDA Submissions Lead

Agence PROvidence; Seattle (WA); On-site; USD 65,000 - 90,000; Full time

Job summary

Providence Swedish is seeking a Regulatory Coordinator to prepare, facilitate, coordinate, and submit documentation required by federal, state, and local regulations related to research conduct. You will lead Research Assistants, provide on-the-job training, and manage priorities to support project objectives and ensure protection of human subjects.

Responsibilities include coordinating IRB submissions, FDA-related filings, and other regulatory documents, with a focus on compliance and timely

Qualifications

• Bachelor's degree in science, healthcare, pharmacy, or related field, or significant experience in research coordination or regulatory work.
• 2 years of healthcare, research or clinical setting with regulatory compliance familiarity.

Responsibilities

• Lead the work of Research Assistants on a task-basis.
• Prepare and submit documentation to IRB and regulatory submissions to ensure protection of human subjects.
• Provide on-the-job training, set priorities and schedules workflow to support project objectives.

Skills

Regulatory compliance

Research coordination

IRB submissions

Education

Bachelor's degree in science/healthcare or related field

Job description

Providence Swedish is seeking a Regulatory Coordinator to prepare, facilitate, coordinate, and submit documentation required by federal, state, and local regulations related to research conduct. You will lead Research Assistants, provide on-the-job training, and manage priorities to support project objectives and ensure protection of human subjects.

Responsibilities include coordinating IRB submissions, FDA-related filings, and other regulatory documents, with a focus on compliance and timely