Senior Clinical Research Associate (Contractor) - UK

Tigermed; Leeds; On-site; GBP 40,000 - 56,000; Full time

Job summary

Tigermed in Leeds, United Kingdom, is seeking a Clinical Research Associate to oversee site management, initiation visits, and monitoring for multiple studies. The role requires a strong CRA background, GCP knowledge, and experience with study documentation and safety reporting.

The candidate will train site staff, coordinate materials, and manage budgets and contracts with sites, ensuring timely SAE reporting and regulatory compliance.

Qualifications

• Bachelor degree or above in Medical, Pharmacology or Biology related major.
• At least 8 years of CRA experience.
• Strong understanding of Good Clinical Practice and trial operation processes.
• Proficient in Microsoft Word, Excel, PPT and Outlook.

Responsibilities

• Site management including site selection, initiation (SIV) and clinical monitoring.
• Conduct pre-study visits to verify site eligibility per criteria.
• Prepare and conduct SIV training for site staff.
• Ensure safety reporting aligns with protocol, SOP, ICH-GCP and GCP.
• Track study recruitment targets across studies.
• Perform monitoring visits and address site issues with timely reports.
• Coordinate study materials and EC submission dossiers.
• Provide ongoing training on ICH-GCP and protocol requirements.
• Maintain essential documents and archiving in trial master files.
• Manage study budgets and contracts with sites.
• Update and maintain study tools and systems.
• Ensure SAE reporting within required timelines.

Skills

CRA experience

GCP knowledge

Education

Bachelor degree or above in Medical, Pharmacology or Biology related major

Tools

Microsoft Word

Excel

PowerPoint

Outlook

Job description

Tigermed in Leeds, United Kingdom, is seeking a Clinical Research Associate to oversee site management, initiation visits, and monitoring for multiple studies. The role requires a strong CRA background, GCP knowledge, and experience with study documentation and safety reporting.

The candidate will train site staff, coordinate materials, and manage budgets and contracts with sites, ensuring timely SAE reporting and regulatory compliance.