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Clinical Trials jobs in Merthyr Tydfil

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    • Previous experience within a pharmaceutical, healthcare, clinical trials or other regulated environment.
    • Act as the main point of contact for allocated clients…
    • Approximately 70 to 80% of the position will focus on QA activities, particularly internal auditing and document control, with the remaining time supporting…
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    • Position: Analytical Chemist, Quality Control.
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    • Experience of working for the NHS, and/or in a clinical research environment would also be desirable as would knowledge of patient confidentiality.
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    • (i.e., GCP, EMA and FDA).
    • You will bring a pragmatic and professional approach to software development, balancing technical quality with reliable delivery in a clinical research setting.
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    • We are looking for a qualified Solicitor with proven Clinical Negligence experience and a strong track record of managing their own caseload.

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clinical research
Logistics Specialist
Up to £40,000 a year
Permanent, Full-time

Job details

Up to £40,000 a year
Life insurance, Free parking, Company pension, On-site parking
Permanent, Full-time
Rhymney

Full job description

Focused Recruitment are currently seeking an experienced Logistics Project Manager to join our clients manufacturing team based out of their site in Rhymney.

The successful person would ideally have experience within the Clinical / Pharmaceutical industry with proactive logistics experience. Able to coordinate international shipments, manage customs/documentation, communicate confidently with clients, and make sure materials get where they need to go — accurately, compliantly and on time.

Hours of work include:

Monday - Thursday 08:30AM - 17:00PM. 08:30AM - 14:00PM on Fridays.

Fully on site working required initially, however following successful probationary period there will can opportunity for flexible working arrangements.

Duties of the role will include:

  • Act as the main point of contact for allocated clients and clinical studies, providing clear and timely updates.
  • Coordinate international shipments from origin to destination, working closely with couriers, freight forwarders, customs brokers and other logistics partners.
  • Prepare, review and manage shipping, customs and import/export documentation, ensuring accuracy and compliance.
  • Support customs classification and the correct application of duties, taxes, Incoterms and HMRC requirements.
  • Coordinate the distribution, retrieval, return and destruction of clinical trial materials in line with project and client requirements.
  • Review shipment and project information, identify missing or incorrect documentation, and provide appropriate shipping advice.
  • Monitor shipments, proactively manage delays or issues, and recommend practical solutions.
  • Maintain accurate logistics reports, records and invoicing information.
  • Ensure all activities comply with company SOPs, client requirements and applicable GMP/GDP regulations.
  • Support wider logistics and departmental projects as required.

Desired criteria:

  • Previous experience within a pharmaceutical, healthcare, clinical trials or other regulated environment.
  • Experience using SAP or similar ERP/logistics systems.
  • Dangerous Goods (DG) training or certification.
  • Experience managing international shipments and customs processes.
  • Working knowledge of GMP/GDP requirements and regulated supply chains.
  • Previous experience working with clinical trial materials or temperature-controlled shipments.
  • A valid UK driving licence.
  • Flexibility to support occasional UK and international travel.

Pay: Up to £40,000.00 per year

Benefits:

  • Company pension
  • Free parking
  • Life insurance
  • On-site parking

Work Location: In person

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