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Clinical Trial jobs in Cheshire

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    • Experience within clinical research, healthcare, laboratories or biobanks.
    • This is an exciting opportunity to play a key role in supporting clinical research by…
    • With experience working in academic clinical trials or clinical research within the NHS.
    • Advise and negotiate on clinical trial agreements including financial…
    • § To liaise with the stakeholders and other project representatives to determine precise requirements in terms of specification and other clinical or user-based…
    • Demonstrate research knowledge when caring for patients receiving treatment within the context of a clinical trial protocol.
    • To have full oversight of clinical trial submission process within teams and overall responsibility from feasibility through to closing out of a team portfolio…
    • Manage selected clinical negligence matters where appropriate.
    • You’ll handle a mix of EL, PL and RTA claims, together with selected clinical negligence matters,…
    • Serving meals to patients at ward level.
    • Ensuring all Food Hygiene and Health & Safety policies and allergen control procedures are followed.
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    • Removal clinical and general waste.
    • Removal of clinical and general waste from ward and department to designated waste store.
    • Cleaning baths, taps, and showers.
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    • Participate in clinical trial feasibilities and risk assessments of clinical trial protocols.
    • Arrange and facilitate clinical trial related meetings.
    • Collaborate with Marketing, Sales, and Sales Operations to refine molecule (mAb) information and monitor updates as prospective biotech companies advance their…
    • The unit undertakes and delivers clinical trials/studies in patients and healthy volunteers for commercial, non-commercial and sub contract studies.
    • Deliver pharmaceutical samples and clinical trial materials to nominated delivery points across the UK.
    • SGS’s Life Sciences services support the pharmaceutical,…
    • Broad understanding of key project functions, including regulatory, quality, manufacturing, clinical, commercial and marketing.
    • Demonstrable experience of dealing with litigated files from inception, through applications and challenges, to trial / disposal hearing.
    • Demonstrable experience of dealing with litigated files from inception, through applications and challenges, to trial / disposal hearing.

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Job Post Details

Clinical Research & Biobank Donor Co-ordinator - job post

BioGrad
4.0 out of 5 stars
Liverpool L13 1HN
£28,000 - £32,000 a year - Part-time, Full-time

Job details

Pay

  • £28,000 - £32,000 a year

Job type

  • Part-time
  • Full-time

Location

Liverpool L13 1HN

Full job description

Clinical Research & Biobank Donor Coordinator

Salary: £28,000 - £32,000 per annum (pro rata for part-time hours)
Location: Liverpool
Job Type: Full-time or Part-time

About BioGrad Biobank

BioGrad Biobank is looking for a compassionate, organised and professional Clinical Research & Biobank Donor Coordinator to join our growing Scientific Operations team.

This is an exciting opportunity to play a key role in supporting clinical research by coordinating donors, collecting biological samples and ensuring the highest standards of patient care, governance and quality.

The successful candidate will have strong administrative skills alongside practical phlebotomy experience and will work closely with donors, researchers and laboratory teams to support ethically approved research projects.

The Role

You will coordinate the safe, ethical and efficient collection of human biological samples for BioGrad Biobank.

This includes:

  • Coordinating donor enquiries and appointments
  • Supporting donor recruitment and pre-screening activities
  • Providing approved study information to participants
  • Obtaining informed consent (where trained and authorised)
  • Performing venepuncture and approved biological sample collection
  • Maintaining accurate donor and study records
  • Supporting research studies from set-up through to completion
  • Ensuring compliance with Good Clinical Practice (GCP), Human Tissue Authority (HTA) requirements, Research Ethics approvals and BioGrad quality procedures

Key Responsibilities

Donor Coordination

  • Coordinate donor enquiries and appointments
  • Manage appointment bookings, confirmations and follow-up communications
  • Act as the main point of contact throughout the donor journey
  • Prepare participant information packs and consent documentation
  • Coordinate appointments with laboratory and scientific teams
  • Maintain accurate donor records
  • Produce activity reports

Clinical Sample Collection

  • Perform venepuncture safely and professionally
  • Verify donor identity and consent
  • Explain procedures and reassure donors
  • Monitor donor wellbeing
  • Label, package and transfer samples
  • Maintain traceability and report incidents

Research Study & Quality Support

  • Support study set-up and monitoring
  • Maintain controlled documentation
  • Support audits and quality improvement
  • Monitor stock and consumables

General Duties

  • Work collaboratively across teams
  • Maintain confidentiality
  • Complete mandatory training including GCP, phlebotomy, safeguarding, first aid and information governance
  • Maintain a safe donor environment
  • Support continuous improvement

Essential Requirements

  • Minimum two years' practical phlebotomy experience
  • Current or recent competency in venepuncture
  • Current Good Clinical Practice (GCP) certification
  • Experience working with patients, donors or research participants
  • Strong administration and organisational skills
  • Excellent communication skills
  • High attention to detail
  • Microsoft Office skills
  • GCSE English and Maths (or equivalent)

Desirable

  • Healthcare, Nursing, Biomedical Science or Life Science qualification
  • Experience within clinical research, healthcare, laboratories or biobanks
  • Knowledge of the Human Tissue Act and Research Ethics processes
  • Experience supporting audits and quality management systems

What We Offer

  • Competitive salary
  • Full-time or part-time opportunities
  • Professional development
  • Supportive working environment
  • Career progression

Pre-employment Requirements

  • Right to Work in the UK
  • Enhanced DBS check
  • Two satisfactory employment references, including the most recent employer
  • Occupational health clearance appropriate to the role

Pay: £28,000.00-£32,000.00 per year

Work Location: In person

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