Clinical Research Regulatory Coordinator

Swedish; Seattle (WA); Hybrid; USD 43,000 - 66,000; Full time

Job summary

Providence Swedish is seeking a Regulatory/Research Coordination Specialist to prepare and submit documentation for IRB and regulatory agencies, ensuring human subjects protection and compliance. You will lead RAs, train staff, set priorities and coordinate timelines in a hybrid Seattle area role.

Responsibilities cover collaboration with clinical teams, managing submissions for FDA-related documents, and ensuring alignment with institutional and regulatory requirements.

Qualifications

• Bachelor's degree in science, healthcare, pharmacy, or related field; or significant research/regulatory experience may substitute.
• 2 years experience in healthcare, research or clinical settings with regulatory familiarity.

Responsibilities

• Prepares, facilitates, coordinates, and submits regulatory documentation to IRB, FDA and institutional requirements.
• Leads Research Assistants on task-basis, provides on-the-job training, sets priorities and schedules workflow.

Skills

Regulatory compliance

Research coordination

Education

Bachelor's degree in science/healthcare/pharmacy or related

Job description

Providence Swedish is seeking a Regulatory/Research Coordination Specialist to prepare and submit documentation for IRB and regulatory agencies, ensuring human subjects protection and compliance. You will lead RAs, train staff, set priorities and coordinate timelines in a hybrid Seattle area role.

Responsibilities cover collaboration with clinical teams, managing submissions for FDA-related documents, and ensuring alignment with institutional and regulatory requirements.