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Description This is a combined posting for an Associate Clinical Research Analyst and Senior Clinical Research Analyst. The requirements of each role are listed below under each associated title. Consideration for each role will be based on qualifications. If you have the qualifications for any one of these three positions, we encourage you to apply. This position does have remote work/work from home but you must be within the Puget Sound/Seattle, WA area. 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. 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. Duties require the use of judgment and independent interpretation and application of relevant Federal and State laws and regulations and institutional policies and guidelines. This requires considerable exercise of independent judgment related to situations of a sensitive, confidential and scientific nature. Providence caregivers are not simply valued - they're invaluable. Join our team at Swedish Research 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. Associate Clinical Research Analyst 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 Experience in healthcare, research or clinical setting with regulatory compliance familiarity. Associate Clinical Research Analyst, Salary Range: Seattle, WA Min: $30.81, Max: $48.06 Senior Clinical Research Analyst Required Qualifications: Bachelor's Degree Or Five or more years of education or experience in clinical research and regulatory affairs may be accepted in lieu of the degree requirement. 5 years Experience in healthcare, research or clinical setting. Senior Clinical Research Analyst, Salary Range: Seattle, WA Min: $38.67, Max: $61.22 Why Join Providence? 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. About Providence At Providence, our strength lies in Our Promise of "Know me, care for me, ease my way." Working at our family of organizations means that regardless of your role, we'll