A clinical research nurse does not perform the same duties as a registered nurse. A registered nurse may eventually want to become part of a clinical research trial to increase her knowledgebase and exposure to the medical world. The work of a clinical research nurse is far from easy. The need to be diligent and possess an analytic mind is high at this point, and you have to do all that you can to be meticulous and accurate.
Clinical research nurses work quite closely with both patients and physicians, so they have to possess great interpersonal skills. It is imperative for clinical research nurses to have a valid nursing license, along with a degree in nursing if they want to work at this position. Some hospitals may require experienced clinical research nurses, but this largely depends on the type of clinical research in question.
Since patients are the subjects of clinical researches, it is imperative for clinical research nurses to look out for their comfort and wellbeing before, during and after each clinical trial. Teamwork and the ability to communicate findings effectively are also prerequisites of working as a clinical research nurse. So if you are interested in a role that will provide you with an opportunity to assist in the design and implementation of clinical researches, you may want to look at the set of duties listed below:
• Interview patients and consider their documents to determine if they meet protocol inclusion criteria
• Draft consent and data collection forms and assist patients or subjects in filling them out
• Perform initial assessments by obtaining medical, mental health, substance abuse and medication histories
• Review intake assessments with clinical team members to gauge patients’ / subjects’ conditions, readiness and study eligibility
• Establish and implement appropriate plan of care for each patient according to his or her specific requirements during the clinical study
• Order, follow up and interpret appropriate lab and diagnostic reports to develop and implement individualized care plans
• Provide patients with information on participation protocols and ensure that they possess deep understanding of the clinical trial program that they will be participating in
• Schedule clinical procedures and follow up appointments through telephone calls and home visits
• Act as a bridge between patients and doctors in order to refer patients for additional care outside of research spectrums
• Write case reports for assigned patients and evaluate them for accuracy and compliance to protocol
• Maintain clinical research data by collecting and inputting it into the database in an accurate and confidential manner