Senior Clinical Research Associate – UK

Tigermed; Norwich; On-site; GBP 55,000 - 75,000; Full time

Job summary

Tigermed is seeking an experienced Clinical Research Associate to lead site management activities in the UK. You will oversee site initiation, monitoring visits, and training to ensure protocol compliance and data integrity.

Key duties include study start-up, regulatory submissions, safety reporting, and collaboration with investigators, with a focus on quality, timeliness and study governance.

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: site selection, initiation (SIV) and clinical monitoring; ensure trial start-up readiness.
• Training: provide ongoing training on ICH-GCP, GCP, protocol and requirements; conduct site initiation.
• Documentation: collect essential documents, maintain investigator files and trial master files; archiving per protocol.
• Drug Safety: ensure safety information dissemination and SAE reporting within SOP timelines.
• Finance and Administration: finalize budgets, contract from sites, manage study payment schedules.
• Study Tools and System: update and maintain study tools and systems.

Skills

MS Word

MS Excel

MS PowerPoint

Outlook

Education

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

Job description

Tigermed is seeking an experienced Clinical Research Associate to lead site management activities in the UK. You will oversee site initiation, monitoring visits, and training to ensure protocol compliance and data integrity.

Key duties include study start-up, regulatory submissions, safety reporting, and collaboration with investigators, with a focus on quality, timeliness and study governance.