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    • Familiarity with clinical trial regulations and Good Clinical Practice (GCP) guidelines is advantageous but not essential.
    • Must hold a valid NMC registration.*.
    • This role oversees operational logistics for clinical trial drug supply and laboratory samples.
    • Understanding of GCP, clinical trial workflows, and IP…
    • You will liaise with clinical investigators, sponsor companies and external vendors to manage trial protocols.
    • Occasional out of hours working may be required.
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    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
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    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
    • Research Grid (R.grid) is the automation engine for admin-free clinical trials.
    • Maintain strong market knowledge to spot emerging players and partnership trends…
    • By conducting audits of our clinical investigator sites, external vendors, and internal trial management processes, you identify the findings and non-compliance…
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    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
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    • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
    • To gain experience of the clinical trial process and become proficient in all aspects of clinical trial coordination.
    • Laboratory sample preparation and storage.
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    • You have successfully managed multiple clinical trial protocols across diverse investigative sites.
    • IQVIA has access to significant data pools allowing better…
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    • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
  • View similar jobs with this employer
    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
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    • Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes.
    • Proficiency in Microsoft Office and clinical trial systems (eTMF, CTMS, EDC)…
    • Provision of medical care and oversight of clinical trial participants.
    • Assist clinical staff members in various clinical activities as required.

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Job Post Details

Clinical Research Nurse - job post

Velocity Clinical Research, Inc.
Eastern Road, Romford RM1 3PJ
£40,000 - £50,000 a year - Temporary, Full-time

Job details

Pay

  • £40,000 - £50,000 a year

Job type

  • Temporary
  • Full-time

Location

Eastern Road, Romford RM1 3PJ

Benefits

Pulled from the full job description

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

Full job description

Job Overview

No experience necessary, would suit a nurse looking to break into clinical research!!

Must hold a valid NMC registration.

Temporary Role for 8 week with potential to be extended

. 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.

Duties

  • 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.

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.

Pay: £40,000.00-£50,000.00 per year

Benefits:

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

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)

Work Location: In person

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