Senior Clinical Research Associate, UK - Contract

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

Job summary

Tigermed is seeking an experienced CRA to oversee site management, training, documentation, safety reporting, finance, and tool maintenance across multiple studies. The role requires in-depth knowledge of ICH-GCP and clinical trial operations, with 8+ years of CRA experience and strong MS Office skills.

Responsibilities include SIV, site initiation, monitoring, and ensuring compliance, safety reporting, budget finalisation, and timely study materials coordination.

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.
• Strong skills in MS Word, Excel, PPT and Outlook.

Responsibilities

• Site management including site selection, initiation (SIV) and clinical monitoring.
• Provide ongoing training to site staff on ICH-GCP, protocol and study requirements.
• Maintain essential documents and trial master files, and ensure archiving.
• Disseminate safety information and report SAEs within SOP timelines.
• Finalise budgets and manage study payment schedules with sites.
• Update and maintain study tools and systems in a timely manner.

Skills

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Outlook

Education

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

Job description

Tigermed is seeking an experienced CRA to oversee site management, training, documentation, safety reporting, finance, and tool maintenance across multiple studies. The role requires in-depth knowledge of ICH-GCP and clinical trial operations, with 8+ years of CRA experience and strong MS Office skills.

Responsibilities include SIV, site initiation, monitoring, and ensuring compliance, safety reporting, budget finalisation, and timely study materials coordination.