Research Nurse (Maternity Leave) at Liverpool School of Tropical Medicine
Liverpool, England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

28 Apr, 25

Salary

0.0

Posted On

16 Apr, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

MAR20253252

Expiry date:

06:00, Mon, 28th Apr 2025
Location:

Liverpool
Salary:

£37,338.00 - £44,962.00 Per Annum
Benefits:

30 days annual leave, plus bank holidays and additional Christmas closure days
Duration:
Fixed-term, maternity cover until 18th May 2026
The Liverpool School of Tropical Medicine (LSTM) is a world leader in infectious disease research, and our Human Challenge Facility (HCF) plays a key role in accelerating the development of vaccines, diagnostics, and therapeutics that improve global health. Our Controlled Human Infection Models are at the forefront of clinical research, shaping the future of infectious disease treatment and prevention.
We are seeking a Research Nurse to join our dynamic team, supporting the delivery of clinical trials in the Accelerator Research Clinic, an 18-bedded outpatient research facility, and the Human Challenge Facility, a 12-bedded inpatient isolation unit. You will play a key role in participant recruitment, clinical assessments, and data collection, ensuring compliance with Good Clinical Practice (GCP) and maintaining the highest standards of patient care.

Responsibilities

CLINICAL RESPONSIBILITIES

  • Conduct research visits, clinical assessments, and procedures such as venepuncture, vital signs monitoring, and respiratory sampling.
  • Assist in research bronchoscopies, ensuring safe patient care.
  • Administer treatments and investigational drugs as per study protocols.
  • Manage caseloads of study participants, ensuring safety monitoring.
  • Coordinate participant follow-ups and ensure timely reporting of results.

ADMINISTRATIVE & OPERATIONAL DUTIES

  • Ensure accurate data collection and documentation in electronic case report forms (eCRFs).
  • Support study setup, documentation, and maintenance of site files.
  • Manage medical supplies and consumables for clinical studies.
  • Assist in archiving clinical studies and maintaining recruitment records.
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