Regulatory Clinical Research Coordinator – IRB/FDA Submissions

Providence Health & Services; Seattle (WA); On-site; USD 43,000 - 66,000; Full time

Benefits offered by this job

Benefits package

Job summary

Providence Swedish is seeking a Research Coordinator to prepare, coordinate, and submit regulatory documentation for human subjects research. You will lead Research Assistants and ensure IRB and FDA submissions comply with requirements.

Join a team dedicated to patient-focused care and research excellence within a large health system, with strong benefits and a collaborative work environment.

Qualifications

• Bachelor's degree in science/healthcare or related field preferred, or significant experience in research coordination/regulatory work may substitute for educational requirements
• 2 years of experience in healthcare, research or clinical setting with regulatory compliance familiarity

Responsibilities

• Prepare, facilitate, coordinate, and submit documentation required by regulations and institutional requirements relating to research
• Lead the work of Research Assistants on a task basis and provide on-the-job training, set priorities and schedules to support project objectives

Education

Bachelor's degree in science/healthcare or related field, or significant experience in research coordination/regulatory work

Job description

Providence Swedish is seeking a Research Coordinator to prepare, coordinate, and submit regulatory documentation for human subjects research. You will lead Research Assistants and ensure IRB and FDA submissions comply with requirements.

Join a team dedicated to patient-focused care and research excellence within a large health system, with strong benefits and a collaborative work environment.