Clinical Research Associate

3 weeks ago


Plymouth, Plymouth, United Kingdom University Hospitals Plymouth NHS Trust Full time
Job Summary

University Hospitals Plymouth NHS Trust is seeking a highly motivated and organized Research Nursing Associate to join our Research and Development team. The successful candidate will be responsible for delivering high-quality nursing care to patients participating in clinical trials, ensuring the smooth operation of research studies, and contributing to the development of new research initiatives.

Main Responsibilities
  • Deliver effective, specialized, high-quality nursing care to patients participating in clinical trials.
  • Work under the supervision of a Registered Practitioner and adhere to local and national protocols, standard operating procedures, and policies.
  • Collect accurate clinical measures, including standard observations, and maintain comprehensive and up-to-date patient records.
  • Conduct assessments and perform necessary procedures in accordance with study protocol.
  • Accurately collect and record data, ensuring it complies with study protocol and Good Clinical Practice (GCP) guidelines.
  • Support the planning and coordination of clinical research studies, including identifying eligible patients and screening potential participants.
  • Provide high-quality and compassionate care to patients participating in clinical trials, including obtaining informed consent and conducting assessments.
  • Collaborate effectively with the research team, including the Principal Investigator, to ensure the successful delivery of research studies.
  • Participate in training sessions, workshops, and conferences to enhance clinical research skills and knowledge.
Requirements
  • GCSEs including English, Maths, and Science at grade A-C/grade 4-9.
  • Foundation degree (FdSc in Healthcare Practice (Nursing Associate) or working towards).
  • Evidence of continuing professional development.
  • Clinical skills, including venepuncture and cannulation or a willingness to undertake.
  • Ability to collect accurate clinical measures, including standard observations.
  • Understanding of ethical practice and patient confidentiality.
  • Good report writing with a focus on accuracy and meticulous attention to detail.
Working Arrangements

The successful candidate will be required to work flexibly, including occasional evenings and weekends, to meet the needs of the research studies.



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