Clinical Research Administration
Embracing the scholar-practitioner (SP) model in clinical research represents a critical responsibility to improve, to inform, and to inspire the lives of others: improve through scholarly research, inform through practical application, and inspire through leadership. During the semester, awareness was heightened as to the importance of scholarly writing, theory implementation, and leadership influence. Being charged with such responsibilities is not for the faint of heart. Becoming independent scholars and critical thinkers who are ready to forge ahead in making valuable contributions to one's fields of expertise requires a great deal of dedication, tenacity, and vision to cultivate a new body of knowledge (Dietzmann, 2005). To become successful, one will need to engage in scholarly writing, which is the basis for the SP model. Without academic integrity, effective writing skills, and synergistic teamwork communicating new knowledge and influencing implementation will not be possible in clinical research.
Academic Integrity
Demonstrating responsible academic behavior is critical to uphold scholarly standards in high-quality research work, academic integrity & honesty, and adherence to ethical guidelines. Clinical researchers are stewards of their learning, while embracing collaborative efforts with colleagues and mentors. Showing care, concern, and professionalism will improve communication, which builds trust for mutually beneficial relationships and professional learning communities (PLCs). Hence, shared values of the clinical research community are to uphold scholarly standards through information literacy, thus building new knowledge.
Becoming an effective scholar requires the assistance of a mentor and a team to provide the guidance needed for success. As a clinical researcher, receiving guidance via constructive feedback will improve knowledge and contribution to the research field in which research and formation experiences are paramount for the development of scholars and for new knowledge communities. More importantly, clinical...
Clinical Research Ethics Medical research is the most sensitive field of research in the entire field of academia. It is governed by several rules, regulations, and ethical standards. For instance, no research endeavor is allowed in case it hurts the life of any human being whether directly or indirectly. Secondly, any research that is to be done must meet environmental conservation measures and should not deride or harm human dignity in
Membership in Professional Organizations Hospitals and other healthcare facilities observe patient experiences for assessing and improving care quality. As nursing professionals devote considerable time to their patients, they greatly influence patient experiences. For providing patients with superior quality healthcare, nursing staff must identify influential factors in the nursing environment. Patients' experiences in the care setting are recognized as markers of care quality assessment and improvement. When patient experiences are gauged by
Letter to Support the Genetic Information Nondiscrimination Act of 2008 (GINA) The Genetic Information Nondiscrimination Act of 2008 (GINA) is an Act of U.S. Congress that makes it illegal for employers and health insurance companies to use genetic information against an individual. For instance, if a person has a genetic predisposition to a particular disease that runs in his or her family tree, an insurer is not allowed to use
Nurse led clinical research: neonatal nurses' perceptions and experiences The aims of the study are to understand the experiences of clinical nurses in conducting and utilizing clinical research within their neonatal setting. This is a qualitative study of five neonatal nurses who were interviewed using semi-structured, face-to-face interviews to obtain the study data. This was a phenomenology-based study, which means it was meant to study the overall structure of the nurses experiences
Roles of Clinical Research Team Members The relevance of a competently constituted clinical research team cannot be overstated when it comes to the success of clinical trials. This is true for both a site-based clinical research team and a sponsor-based clinical research team. Sponsor-Based Clinical Research Team Data Coordinator According to Robinson (2009, p. 9), "the primary role of a data coordinator is to ensure that the clinical trial database is accurate and complete,
Stakeholders in Clinical Research Trials There are various stakeholders involved in clinical trials. These include, but they are not limited to, funding agencies, the patient, the government, regulatory and oversight boards, the general public, insurers (if any), and the industry. In essence, these stakeholders not only influence, but also contribute to the process as well as outcome of clinical trials in a variety of ways. Below, I concern myself with three
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