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    • This role oversees operational logistics for clinical trial drug supply and laboratory samples.
    • Understanding of GCP, clinical trial workflows, and IP…
    • Generous Time Off – 23 days of annual leave to recharge and unwind.
    • Financial Security – Excellent company contributed pension & 4x salary death-in-service…
    • Generous time off – 23 days of annual leave to recharge and unwind.
    • Document control, to include study-specific and general documentation.
    • The postholder will gain extensive experience in the set up and execution of clinical trials and laboratory based / translational research.
    • We are looking for a highly specialist pharmacist with experience in clinical trials, pharmaceutical manufacturing, or regulatory affairs and someone who is…
    • Clinical research: 1 year (required).
    • We are seeking nurse and technician candidates with experience in acute clinical settings such as *Medicine, ITU/CCU,…
    • Provision of medical care and oversight of clinical trial participants.
    • Assist clinical staff members in various clinical activities as required.
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    • Provision of medical care and oversight of clinical trial participants.
    • Assist clinical staff members in various clinical activities as required.
    • Conduct patient assessments and monitor patient responses during clinical trials, ensuring safety and adherence to protocols.
    • Understanding of current relevant clinical and professional issues.
    • Previous experience of clinical research in wound care.
    • Pay: £37,315.00-£39,191.00 per year.
    • Significant experience within clinical research laboratories.
    • Bodyline Medical Wellness Clinics is a leading CQC-registered clinical services and clinical…
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    • Provision of medical care and oversight of clinical trial participants.
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    • Dealing with post issue claims, including instructing, working with barristers and producing bundles…
    • A scientific or clinical background is beneficial but not essential.
    • Working closely with the Data Manager, you will help ensure the successful planning,…
    • Working closely with colleagues across clinical and non-clinical teams, you will help ensure that data, systems, projects and quality processes are effectively…

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Job Post Details

Clinical Trial Coordinator - job post

Iksuda Therapeutics
Newcastle upon Tyne NE4 5BX•Hybrid work
£28,000 - £34,000 a year - Permanent, Full-time
Responded to 75% or more applications in the past 30 days, typically within 5 days.

Job details

Pay

  • £28,000 - £34,000 a year

Job type

  • Permanent
  • Full-time

Shift and schedule

  • Monday to Friday

Location

Newcastle upon Tyne NE4 5BX•Hybrid work

Benefits

Pulled from the full job description

  • Life insurance
  • Company pension
  • Free flu jabs
  • Work from home
  • Flexible schedule

Full job description

Iksuda Therapeutics is a Biotechnology Company focused on the development of Antibody Drug Conjugates (ADCs) for the treatment of cancer.

An exciting opportunity to join our team as a Clinical Trial Coordinator - Drug Supply & Laboratory Sample Logistics, supporting activities and contributing towards Clinical Operations.

This role oversees operational logistics for clinical trial drug supply and laboratory samples. The position ensures timely ordering, receipt, accountability, and reconciliation of investigational product (IP) across global sites, while also managing central and specialty lab workflows, sample labeling compliance, and shipment traceability. The Coordinator works closely with Clinical Operations, clinical supply team, CMC, QA, and external vendors to maintain GCP‑compliant processes that support patient safety, data integrity, and operational efficiency.

Experience required

  • 1-3 years of experience in clinical operations, drug supply management, or central lab logistics

Skills and competencies required

Essential

  • Understanding of GCP, clinical trial workflows, and IP accountability requirements.
  • Excellent organizational, communication, and vendor‑management skills.
  • Ability to manage multiple priorities in a fast‑paced, global environment.
  • Detail‑oriented with a commitment to data integrity and operational excellence.

Desirable

  • Understanding of QA systems
  • Previously employed by a CRO specialising in Clinical Operations/a drug depot/a central lab

Qualifications required

Essential

  • Bachelor’s degree (or equivalent) in a life sciences discipline
  • 1 years’ experience in clinical operations, drug supply management or central lab logistics

Desirable

  • 3 years’ experience in clinical operations, drug supply management or central lab logistics

Schedule:

  • Monday to Friday - Flexible hours

Work Location:

  • This is a hybrid role, predominantly working remotely with the flexibility to attend site meetings as required. Flexible working hours are available, as the role involves collaborating with colleagues across multiple time zones to meet business needs.

MUST have UK Right to Work.

Please include a cover letter with your application.

Pay: £28,000.00-£34,000.00 per year

Benefits:

  • Company pension
  • Free flu jabs
  • Life insurance
  • Work from home

Education:

  • Bachelor's (required)

Experience:

  • clinical operations or central lab logistics: 1 year (required)

Work Location: Hybrid remote in Newcastle upon Tyne NE4 5BX

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