Clinical Trial jobs in Newcastle upon Tyne
Clinical Trial Coordinator
Often replies in 5 daysIksuda TherapeuticsNewcastle upon Tyne NE4 5BX- Life insurance
- Company pension
- Flexible schedule
- Free flu jabs
- Work from home
- This role oversees operational logistics for clinical trial drug supply and laboratory samples.
- Understanding of GCP, clinical trial workflows, and IP…
- Adkins & Cheurfi RecruitmentNewcastle upon Tyne NE1 2LA
- Support solicitors in billing and fee note preparation related to clinical negligence work.
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- Northumbria Healthcare - NHCT Northumbria...North Shields NE29 8NH
- Lead on the recruitment, consent, education and monitoring of patients participating in clinical trials.
- Ensure research activity is embedded within clinical…
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- Health Research AuthorityNewcastle upon Tyne NE2 4NQ
- This supports the government’s pledge to cut the time it takes to get a clinical trial set up to 150 days or less.
- Piramal EnterprisesMorpeth
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- サイネオス・ヘルスNewcastle upon Tyne
- Significant experience in the clinical trial industry, with deep knowledge of the pharmaceutical landscape (required).
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- Maverex LimitedNewcastle upon Tyne NE6 2AR
- Paid training
- Flexitime
- Annual leave
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- Employee assistance programme
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Job Post Details
Clinical Trial Coordinator - job post
Job details
Pay
- £28,000 - £34,000 a year
Job type
- Permanent
- Full-time
Shift and schedule
- Monday to Friday
Location
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