Job Description

The duties and responsibilities will include, but will not be limited to, the following: Research Delivery Coordinate and conduct clinical research study activity and contribute to commercial and non commercial trials as required Ensure that the approved trial protocols are followed at all times Involved in EOI submissions for commercial and non-commercial trials Maintain trial site files Maintain files of current protocols, patient information sheets and consent forms Conduct trials and trial related activities according to current legislation, GCP, study SOPs and Confederation SOPs Apply critical appraisal skills in evaluating research protocol and implementation Assist in the development and maintenance of databases as appropriate Consults with primary investigators, research organisations and industry in the delivery of research protocols Develop knowledge of the preclinical data and the specific rationale for research trials Ensures trial case report forms are completed within appropriate time guidelines Processes blood and tissue samples according to study protocols and standard operating procedures for appropriate work for which the post-holder has been trained Attends research seminars and meetings relevant to research as required Clinical Demonstrates autonomy as well as being a key player within a multidisciplinary healthcare research team Ensure patients are treated according to the schedule or protocol Coordinate and monitor the care of research participants Collaborate with the clinical and corporate staff involved in clinical trials Participate in identifying potential patients for trials Pre screen eligibility of potential patients Ensures all pre study tests are undertaken and results obtained Acts as patient advocate and assist in obtaining informed consent in the first instance and as the trial progresses/unfolds Register and randomise patients onto study protocols Provide general written and verbal information to patients and families on the concept of clinical trials and detailed education regarding the objectives, scientific rationale, treatment and investigations, side effects, self-care and follow-up for specific clinical trials Participate in decisions concerning the treatment of patients on trials in accordance with the protocol. Where appropriate, provide direct patient care within the expanded role of clinical trials (e.g. advanced history taking, toxicity and response evaluation skills, administration of experimental agents, etc) Systematically document patient information in the medical notes ensuring appropriate coding and reporting of data Schedules follow-up appointments, consistent with protocol guidelines Perform, or be willing to be trained to perform spirometry to ARTP standards or equivalent Maintain measurable standards of nursing care for specific needs of patients Administer study drugs as required by the relevant clinical trials and according to study protocols Communication Disseminate protocol information to other healthcare professionals and patients Educate staff and patients about clinical research and its importance Act as one of the primary contacts for patients interested or participating in research Educate patients and their families about clinical research, including objectives, rationale, involvement and outcomes Report and support with the reporting of any adverse events or serious adverse events Management Act as an appropriate and effective nursing role model at all times Act as a resource, supporting and motivating staff members involved in research delivery Take personal responsibility for promoting a safe environment and safe patient care by identifying areas of risk and following the incident, serious incidents and near misses Professional Practice in accordance with the NMC code of professional conduct at all times Adheres to organisational policies, procedures, standards and protocols Remains up to date professionally as outlined by the NMC Training & Development Ensure all organisational mandatory training is completed and up-to-date Maintain own professional development Attend any organisational or research workshops, conferences etc as required