I have extensive experience in ethical review processes, having worked with various research protocols across multiple disciplines. I am well-versed in the regulations set forth by the Department of Health and Human Services, including the Common Rule. My role involved ensuring that all studies adhered to ethical standards, protecting both participants and the integrity of the research.

Handling conflicts of interest is crucial. I ensure transparency by requiring all researchers to disclose any potential conflicts. These disclosures are then reviewed and managed to prevent bias. If a conflict is identified, I work with the team to develop a mitigation plan, ensuring that the conflict does not compromise the study's outcomes or the participants' well-being.

I employ clear, concise communication strategies, using analogies and real-world examples to explain complex ethical concepts. I also utilize visual aids like flowcharts and infographics to simplify information. Engaging stakeholders through interactive discussions helps ensure they fully understand the ethical implications and the importance of adhering to ethical guidelines.

In such a situation, I would first ensure that the concerns are thoroughly documented and communicated to the research team. I would then facilitate a discussion to address the issues, possibly revising the protocol to align with ethical standards. If necessary, I would recommend suspending the study until the necessary changes are made and approved by the IRB.

In a previous role, I encountered a study where the informed consent process was inadequate. I worked closely with the research team to redesign the consent forms and educate them on best practices for obtaining informed consent. This collaborative approach ensured that the study could proceed ethically, safeguarding the rights and welfare of the participants.