Senior CRA — Site Management & Safety Oversight

Tigermed; Southampton; On-site; GBP 42,000 - 64,000; Full time

Job summary

Tigermed is seeking a senior Clinical Research Associate to lead site management, monitoring, and compliance activities for UK studies from our Southampton team. You will oversee site selection, SIVs, staff training, and adherence to ICH-GCP and protocol requirements.

You will monitor recruitment, manage safety communications, and coordinate budgets, contracts, and study tools to ensure timely study delivery and data integrity. Strong MS Office skills are essential.

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

• Study site selection, initiation (SIV) and clinical monitoring.
• Ensure site staff training on protocol and regulations.
• Coordinate study materials and EC submission to EC.
• Track recruitment to meet targets.
• Conduct monitoring visits and address site issues.
• Coordinate EC submission dossier to EC.
• Disseminate safety information to sites per SOPs.
• Report SAE within timelines.
• Finalize budget and obtain signed contracts prior to site initiation.
• Ensure study payment schedule and retain receipts.
• Update and maintain study tools/systems.

Skills

CRA coordination

GCP knowledge

Clinical trial operations

Education

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

Tools

Microsoft Word

Excel

PowerPoint

Outlook

Job description

Tigermed is seeking a senior Clinical Research Associate to lead site management, monitoring, and compliance activities for UK studies from our Southampton team. You will oversee site selection, SIVs, staff training, and adherence to ICH-GCP and protocol requirements.

You will monitor recruitment, manage safety communications, and coordinate budgets, contracts, and study tools to ensure timely study delivery and data integrity. Strong MS Office skills are essential.