Senior UK CRA Contractor – Clinical Trials Lead

Tigermed; Chesterfield; On-site; GBP 50,000 - 70,000; Full time

Job summary

Tigermed is seeking an experienced Clinical Research Associate in the United Kingdom to oversee site management, training, documentation, and safety reporting across multiple studies. The candidate will coordinate SIVs, ensure regulatory compliance, and support budget and contracting activities.

Proficiency in MS Office and GCP is essential. The role requires strong organizational skills, attention to detail, and the ability to manage study materials and systems efficiently within a busy

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: study site selection, initiation visits, and ongoing monitoring to ensure protocol compliance.
• Provide site training on ICH-GCP, protocol requirements and study procedures.
• Maintain essential documentation and trial master files from start-up through close-out.
• Ensure SAE reporting within SOP timelines and regulatory requirements.
• Manage study budgets and contract signatures prior to initiation visits.
• Update and maintain study tools and systems in a timely manner.

Job description

Tigermed is seeking an experienced Clinical Research Associate in the United Kingdom to oversee site management, training, documentation, and safety reporting across multiple studies. The candidate will coordinate SIVs, ensure regulatory compliance, and support budget and contracting activities.

Proficiency in MS Office and GCP is essential. The role requires strong organizational skills, attention to detail, and the ability to manage study materials and systems efficiently within a busy