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Regulatory Affairs Specialist
2 months ago
Job Summary:
Swedish Cherry Hill is seeking a highly skilled Regulatory Affairs Specialist to join our Clinical Research team. As a key member of our team, you will be responsible for preparing, coordinating, and submitting required documentation for research compliance with regulations at all levels.
Key Responsibilities:
- Prepare and submit documentation to IRB to ensure human subjects protection
- Coordinate and submit FDA-required documentation and other necessary paperwork for regulatory agencies
- Oversee Research Assistants' work and provide training and guidance as needed
Requirements:
- Bachelor's Degree in science, healthcare, or related field, or equivalent experience in research coordination or regulatory affairs
- Minimum of 2 years experience in healthcare, research, or clinical settings with knowledge of regulatory compliance
Why Providence?
At Providence, we value our caregivers and prioritize their well-being, professional growth, and financial stability. Our benefits are designed to support you and your family's needs, allowing you to focus on delivering exceptional patient care.
