Contract CRA – UK: Site Management & Study Oversight

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

Job summary

Tigermed is seeking an experienced Clinical Research Associate (CRA) to manage site initiation, monitoring, and data collection across studies in line with protocol and regulatory standards.

The role requires strong knowledge of GCP and trial operations, with responsibility for site qualification, training, and supplier coordination. You will monitor safety reporting and ensure compliant documentation throughout trial conduct.

Qualifications

• Bachelor degree or above in Medical, Pharmacology or Biology related major.
• At least 8 year 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 management responsibilities including study site selection, initiation (SIV) and clinical monitoring.
• Ensure safety reporting requirements are followed per protocol, SOP, ICH-GCP and GCP.
• Manage budgets, contracts and study payment schedules.
• Oversee study tools and systems; ensure timely documentation and archiving.
• Provide ongoing training to site staff on GCP, protocol, and requirements.
• Conduct site initiation to ensure understanding of the study protocol.

Skills

Clinical trial operations

GCP knowledge

Documentation

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Outlook

Education

Bachelor degree in Medical, Pharmacology or Biology related major

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Outlook

Job description

Tigermed is seeking an experienced Clinical Research Associate (CRA) to manage site initiation, monitoring, and data collection across studies in line with protocol and regulatory standards.

The role requires strong knowledge of GCP and trial operations, with responsibility for site qualification, training, and supplier coordination. You will monitor safety reporting and ensure compliant documentation throughout trial conduct.