Band 5 Clinical Research Practitioner

Company: National Health Service
Apply for the Band 5 Clinical Research Practitioner
Location: Birmingham
Job Description:

Overview

As a Band 5 Clinical Research Practitioner at the CRF, you will coordinate the IBHO BioResource while supporting early-phase clinical studies. You will engage with diverse communities, manage study processes, and ensure regulatory compliance in a dynamic research environment. This role offers hands-on participant-facing work and data management across a range of diseases, with a focus on improving health outcomes for UK Black communities. You will work closely with colleagues and external partners to drive inclusive research participation and high-quality trial delivery.

Pay / Benefits

  • flexible working
  • permanent contract
  • £32,073–£39,043 salary (Band 5)
  • inclusive workplace
  • opportunity to contribute to health inequality initiatives

Responsibilities

  • Coordinate and deliver the IBHO BioResource and support early-phase CRF studies
  • Identify/screen potential participants and obtain informed consent
  • Collect/process blood and tissue samples; record vitals; perform ECGs and phlebotomy
  • Maintain Investigator Site Files and manage study data
  • Respond to data queries and assist sponsor monitoring visits
  • Ensure procedures align with study protocol and regulatory requirements
  • Engage with participants and collaborate with colleagues and external partners
  • Contribute to reducing health inequalities through research activities

Key requirements

  • Significant experience in clinical trial/research data management
  • Experience of research in a healthcare setting
  • Understanding of research governance and GCP (ICH GCP)
  • Essential GCSE English and maths; degree-level or diploma-level education in Healthcare, Science or Research
  • Travel and flexible work to meet service needs
  • Excellent interpersonal and communication skills
  • Collaborative and team-oriented
  • Commitment to equality, diversity and inclusion
  • Clinical trial data management
  • Regulatory compliance and study documentation
  • Informed consent process; specimen collection and handling

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Posted: October 10th, 2026