Oncology Research Regulatory Specialist managing regulatory documents and compliance for clinical trials. Supporting a multidisciplinary team within Avera Cancer Institute.
Responsibilities
Works under general direction to perform professional level clinical research assignments.
Prepares and completes regulatory documents for protocols as requested by investigators, sub-investigators and clinical research coordinators.
Submits all required research documents to the protocol sponsor, the Institutional Review Boards (IRB), the FDA, and any other regulatory agency as required by the research project.
Requirements
2 years regulatory, quality or data analyst experience.
Bachelor's degree preferred.
1-3 years related research experience and/or training.
Benefits
PTO available day 1 for eligible hires.
Up to 5% employer matching contribution for retirement.
Career development guided by hands-on training and mentorship.
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