The Regulatory Advisor acts as a central resource, guiding researchers on preparing and submitting documentation for human subjects research, especially FDA-regulated and sponsor-funded clinical trials, to the Institutional Review Board (IRB). This role involves advising on study design, translating research ideas into compliant protocols, and developing educational materials regarding regulatory requirements and IRB navigation.

Design and execute a comprehensive risk and compliance strategy, provide senior advisory on regulatory matters, oversee compliance with applicable regulations, and lead a high-performing risk and compliance organization to foster a culture of ethical...

The EHS Associate II (Loss Control Associate) plays a key role in managing and supporting loss control and return-to-work programs within American Red Cross Biomedical Services. This fully remote position helps reduce workplace injuries, improve incident reporting, and control co...

Develop and execute comprehensive test strategies and plans for compliance software applications, collaborating with stakeholders to translate requirements into test cases while identifying defects and assessing software quality from an end-user...