Clinical Research Nurse

at  Velocity Clinical Research Inc

JOB OVERVIEW

We are seeking a dedicated and knowledgeable Research Nurse to join our clinical research team. The ideal candidate will play a crucial role in the management and execution of clinical trials, ensuring the highest standards of patient care while contributing to vital medical research. This position requires a strong background in nursing, with a particular emphasis on patient interaction and an understanding of human anatomy.

REQUIREMENTS

• Registered Nurse (RN) qualification with a current nursing licence.
• Proven experience in patient care, preferably within a research or clinical setting.
• Strong knowledge of human anatomy and physiology to effectively assess patient conditions.
• Excellent communication skills, both verbal and written, to interact with patients and team members effectively.
• Ability to work independently as well as part of a multidisciplinary team.
• Strong organisational skills with attention to detail for accurate data collection and documentation.
• Familiarity with clinical trial regulations and Good Clinical Practice (GCP) guidelines is advantageous but not essential.
  If you are passionate about advancing medical knowledge through research while providing exceptional care to patients, we encourage you to apply for this rewarding opportunity as a Research Nurse.
  Job Type: Full-time
  Pay: £40,542.00-£42,378.00 per year

Benefits:

• Additional leave
• Company pension
• Enhanced maternity leave
• Enhanced paternity leave
• Health & wellbeing programme
• Life insurance
• On-site parking
• Referral programme
• Sick pay

Schedule:

• Monday to Friday

Application question(s):

• How many years of clinical research experience do you have?

Experience:

• Nursing: 1 year (required)
• Clinical research: 1 year (required)

Licence/Certification:

• NMC (required)
• Driving Licence (preferred)

Work Location: In perso

• Conduct patient assessments and monitor their health status throughout the research study.
• Administer medications and treatments as per study protocols while ensuring patient safety and comfort.
• Collect and document data accurately, maintaining meticulous records for compliance with regulatory requirements.
• Collaborate with physicians, researchers, and other healthcare professionals to facilitate effective study implementation.
• Educate patients about the study procedures, potential risks, and benefits, ensuring informed consent is obtained.
• Participate in the development of research protocols and assist in the preparation of reports for regulatory submissions.
• Maintain confidentiality of patient information in accordance with ethical guidelines and organisational policies.