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    • Iksuda Therapeutics is a Biotechnology Company focused on the development of Antibody Drug Conjugates (ADCs) for the treatment of cancer.
    • Location: *Based between head office and project sites across Kent, with regular travel required.
    • Support the delivery of projects in line with company…
    • Attend project related meetings, investigator meetings (abroad or teleconferences, as necessary) to convey the relevant information to the study team.
    • The individual is responsible for the design, development, testing, validation, execution, & maintenance of clinical studies in the RAMOS Interactive Response…
    • Accountable for all project deliverables for assigned projects and/or project regions.
    • Responsible for project management components of inspection readiness for…
    • Responsible for the project management of all projects either at individual practice level or across our group.
    • You will report to the Groups Business Manager.
    • Proven experience in project management and able to demonstrate project management skills used in the delivery of work.
    • Oversee and resolve operational aspects of clinical trials in conjunction with project teams.
    • Minimum of 5 years of experience in clinical project management or…
    • The Programme Scheduler is a critical post within the New Hospital Programme, Norfolk & Waveney University Hospitals Group, with responsibility for the design,…
    • Responsible for creating and maintaining project timelines for each project and uses these timelines to track and manage a project's progress.
    • Provide senior leadership within a matrix project environment , guiding and mentoring project team members while resolving issues and escalations at pace.
    • Provide senior leadership within a matrix project environment , guiding and mentoring project team members while resolving issues and escalations at pace.
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    • Support compound transfers and project timelines when required.
    • Work closely with project management, operations, logistics and scientific teams to ensure…
    • Stakeholder engagement is an important aspect of this role, with the project administrator acting as a point of contact for all project partners, stakeholders…
    • Previous experience of leading and successfully deliverying projects on time and to budget.
    • This role is funded by the National Institute for Health and Care…

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 51-74% of applications in the past 30 days, typically within 3 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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