Senior Clinical Research Analyst - Tumor Institute

Job description

Prepare, facilitate and coordinate, and submit documents 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. Lead the work of Research Assistants on a task-basis, if applicable. Provide education, on-the-job training, set priorities and schedule 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 or five or more years of education or experience in clinical research and regulatory affairs m...