Associate Clinical Research Analyst - Tumor Institute

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

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.

Providence Swedish caregivers are not simply valued - they're invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.

Required Qualifications:

• Bachelor's degree preferably in science, healthcare, pharmacy, 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

Why Join Providence Swedish?

Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our mission of improving the health and wellbeing of each patient we serve.