Contractor CRA - Site & Study Management (UK)

Tigermed; Nottingham; On-site; GBP 55,000 - 75,000; Full time

Job summary

Tigermed in the United Kingdom is seeking an experienced Clinical Research Associate (CRA) to manage sites, initiate studies, and monitor trials in compliance with protocol and regulatory requirements.

The role requires at least 8 years of CRA experience, strong knowledge of ICH-GCP, and proficiency in Word, Excel, PowerPoint and Outlook. You will coordinate study materials, budgets, and site submissions while maintaining trial master files.

Qualifications

• Bachelor degree or above in Medical, Pharmacology or Biology related major.
• At least 8 years of 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 selection, initiation (SIV) and monitoring.
• Pre-study visits to ensure eligible sites.
• Conduct SIV to train site staff on protocol and requirements.
• Ensure safety reporting per protocol and ICH-GCP.
• Track recruitment targets.
• Perform monitoring visits per SDV plan and file reports.

Skills

GCP knowledge

Clinical trial ops

MS Office

Education

Bachelor degree in Medical/Pharmacology/Biology

Job description

Tigermed in the United Kingdom is seeking an experienced Clinical Research Associate (CRA) to manage sites, initiate studies, and monitor trials in compliance with protocol and regulatory requirements.

The role requires at least 8 years of CRA experience, strong knowledge of ICH-GCP, and proficiency in Word, Excel, PowerPoint and Outlook. You will coordinate study materials, budgets, and site submissions while maintaining trial master files.