Senior Contractor CRA: Site Management & Compliance

Tigermed; Warmley; On-site; GBP 65,000 - 80,000; Full time

Job summary

Tigermed is seeking an experienced Clinical Research Associate (CRA) to lead site management, initiation visits, and ongoing monitoring in accordance with ICH-GCP and protocol requirements. The role focuses on ensuring site readiness, safety reporting, and meticulous trial documentation.

Ideal candidates hold a bachelor's degree in Medical/Pharmacology/Biology, have 8+ years CRA experience, and possess strong skills in Word, Excel, PowerPoint and Outlook to support trial operations.

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 including study start-up and initiation activities, site selection and monitoring.
• Ensure safety reporting and regulatory compliance per protocol and ICH-GCP.
• Manage study materials, budgets, and payments for sites and vendors.
• Maintain study tools and systems, ensure timely documentation and archiving.

Skills

GCP knowledge

Clinical trial operations

Documentation management

Education

Bachelor degree or above in Medical, Pharmacology or Biology

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Outlook

Job description

Tigermed is seeking an experienced Clinical Research Associate (CRA) to lead site management, initiation visits, and ongoing monitoring in accordance with ICH-GCP and protocol requirements. The role focuses on ensuring site readiness, safety reporting, and meticulous trial documentation.

Ideal candidates hold a bachelor's degree in Medical/Pharmacology/Biology, have 8+ years CRA experience, and possess strong skills in Word, Excel, PowerPoint and Outlook to support trial operations.