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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…
    • MUST HAVE: Experience in clinical trials..
    • Patient Assessments:* Perform clinical and cognitive assessments as required by trial protocols (e.g., MMSE, MoCA,…
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    • Knowledge or FDA and ICH-GCP guidelines for conducting clinical research.
    • Work is performed in an office/ laboratory and/or a clinical environment.
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    • Collaboration with experienced clinical and operational professionals.
    • Coordinating project delivery across clinical and operational teams.
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    • Deliver training on Working Practice Documents (WPDs) and Standard Operating Procedures (SOPs), local requirements and any other subjects that impact clinical…
    • Strong clinical credibility and professional standards.
    • Develop and maintain competency frameworks across clinical roles.
    • Travel Required, Full-Time, Permanent.
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    • 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.
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    • Provision of medical care and oversight of clinical trial participants.
    • Assist clinical staff members in various clinical activities as required.
    • Experience in clinical research or clinical trials.
    • Act as Study Physician on selected trials.
    • With over 35 years of experience and a track record of success,…
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    • This is your chance to move into a structured Monday - Friday clinical role with no shifts, no chaos, and no burnout..
    • Message now – roles filling quickly*.
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    • This is your chance to move into a structured Monday - Friday clinical role with no shifts, no chaos, and no burnout..
    • Message now – roles filling quickly*.
    • Significant experience within clinical research laboratories.
    • Bodyline Medical Wellness Clinics is a leading CQC-registered clinical services and clinical…
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    • This is your chance to move into a structured Monday - Friday clinical role with no shifts, no chaos, and no burnout..
    • Message now – roles filling quickly*.
    • This role serves as a GVP Auditor within our Research & Development Quality audit program, responsible for executing the global audit plan to ensure the…

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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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