UK Contract CRA: Site Management & Trial Oversight

Tigermed; Cambridge; On-site; GBP 65,000 - 90,000; Full time

Job summary

Tigermed in Cambridge, United Kingdom, is seeking a qualified Clinical Research Associate to oversee site management, initiation, and monitoring for multiple studies. You will ensure safety reporting, regulatory compliance, and efficient study administration.

The role requires strong knowledge of ICH-GCP, trial operations, and extensive experience with MS Office tools. You will collaborate with site staff to ensure protocol adherence and timely study completion.

Qualifications

• Bachelor degree or higher in medical/biological field required.
• 8+ years of CRA experience required.
• Strong understanding of ICH-GCP and trial operations.
• Proficient in MS Word, Excel, PPT and Outlook.

Responsibilities

• Site management including site selection, initiation (SIV) and clinical monitoring.
• Ensure safety reporting per protocol, SOP, ICH-GCP and GCP.
• Maintain investigator files and trial master files; archiving per protocol.
• Coordinate study materials and EC submissions to sites.
• Provide ongoing training to site staff on ICH-GCP and protocol.

Skills

CRA experience

GCP knowledge

Documentation

Communication

Education

Bachelor degree or above in Medical/Pharmacology/Biology

Tools

Microsoft Word

Excel

PowerPoint

Outlook

Job description

Tigermed in Cambridge, United Kingdom, is seeking a qualified Clinical Research Associate to oversee site management, initiation, and monitoring for multiple studies. You will ensure safety reporting, regulatory compliance, and efficient study administration.

The role requires strong knowledge of ICH-GCP, trial operations, and extensive experience with MS Office tools. You will collaborate with site staff to ensure protocol adherence and timely study completion.