Senior Clinical Research Associate – UK Contract

Tigermed

Bath

On-site

GBP 52,000 - 72,000

Full time

14 days+
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Job summary

Tigermed is hiring an experienced Clinical Research Associate (CRA) for roles in the United Kingdom. The position focuses on site management, initiation visits, training, and documentation to ensure compliant trial conduct according to GCP and protocol requirements.

The ideal candidate has a bachelor degree or higher in medical/biological fields and at least 8 years of CRA experience, with strong skills in MS Word/Excel/PowerPoint/Outlook and a solid understanding of clinical trial operations.

Qualifications

  • Bachelor degree or above in Medical, Pharmacology or Biology related major.
  • 8+ years CRA experience.
  • Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures.
  • Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

Responsibilities

  • Site management including study initiation, monitoring and site selection activities.
  • Provide site training on ICH-GCP and protocol requirements.
  • Maintain study documents and archiving in accordance with SOPs and sponsor requirements.
  • Ensure safety information and SAE reporting in line with regulations.
  • Oversee budget, contracts, and study payments with site staff.
  • Maintain and update study tools and systems timely.

Skills

GCP knowledge
Clinical trial operations

Education

Bachelor degree or above in Medical, Pharmacology or Biology related major
8+ years CRA experience

Tools

Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Outlook

Job description

Tigermed is hiring an experienced Clinical Research Associate (CRA) for roles in the United Kingdom. The position focuses on site management, initiation visits, training, and documentation to ensure compliant trial conduct according to GCP and protocol requirements.

The ideal candidate has a bachelor degree or higher in medical/biological fields and at least 8 years of CRA experience, with strong skills in MS Word/Excel/PowerPoint/Outlook and a solid understanding of clinical trial operations.

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