Senior Clinical Research Associate (Contractor) – UK

Tigermed; Wolverhampton; On-site; GBP 38,000 - 52,000; Full time

Job summary

Tigermed in Wolverhampton, UK, is seeking an experienced Clinical Research Associate to oversee site management, initiation visits and ongoing monitoring for multiple studies. You will coordinate site training, ensure protocol adherence and manage safety reporting with regulatory compliance.

You will track recruitment, liaise with investigators, and maintain study documents and archiving. Proficiency in Word, Excel, PowerPoint and Outlook, plus a solid understanding of ICH-GCP, are essential for

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 clinical monitoring.
• Pre-study visits to ensure eligible sites meet criteria.
• Prepare and conduct SIV to train site staff on protocol and requirements.
• Ensure PI/staff comply with safety reporting per protocol, SOP, ICH-GCP and GCP.
• Track study recruitment to achieve targets across studies.
• Conduct monitoring visits according to SDV plan and SOP; address issues and report.
• Coordinate timely provision of study materials (drug, non-drug, equipment, CRFs) to sites.
• Assemble site-specific EC submission dossier and ensure submission to EC.

Skills

Microsoft Word

Excel

PowerPoint

Outlook

Education

Bachelor degree in Medical, Pharmacology or Biology related major

Tools

Microsoft Word

Excel

PowerPoint

Outlook

Job description

Tigermed in Wolverhampton, UK, is seeking an experienced Clinical Research Associate to oversee site management, initiation visits and ongoing monitoring for multiple studies. You will coordinate site training, ensure protocol adherence and manage safety reporting with regulatory compliance.

You will track recruitment, liaise with investigators, and maintain study documents and archiving. Proficiency in Word, Excel, PowerPoint and Outlook, plus a solid understanding of ICH-GCP, are essential for