Research facility as clinical research coordinator

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Reference no: EM133801749

Question

Experience: "I work for a research facility as a clinical research coordinator and there was a time when I had brought the patient back to one of our clinic rooms to discuss a research trial our company is conducting. We have a process installed at my company where patients have to sign medical consent prior to obtaining medical information and I was unaware of this process and when I brought the patient back to the room I was asking him questions about his medical information without signing an informed consent. We have procedures and protocols placed inorder to maintain efficacy and order of patient rights. After this incident I always have the patient sign consent prior to obtaining their medical history as a way to protect the patients rights along with company policies. " Offer an additional core APHA value that connects to your peer's experience.

Reference no: EM133801749

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