Senior Clinical Research Site Manager (CRA) – UK

Tigermed; Manchester; On-site; GBP 40,000 - 55,000; Full time

Job summary

Tigermed is seeking an experienced Clinical Research Associate in Manchester to oversee site management, training, and documentation across trials in line with ICH-GCP and sponsor requirements. You will ensure site initiation, monitoring visits, safety reporting, and study materials coordination, with a strong focus on regulatory compliance and timely issue resolution.

The role demands at least 8 years in CRA roles, a bachelor-level science degree, and proven MS Office skills.

Qualifications

• Bachelor degree or above in a medical/science field.
• At least 8 years of CRA experience.
• Strong knowledge of GCP and clinical trial operations.
• Proficient in MS Word, Excel, PowerPoint and Outlook.

Responsibilities

• Site management including study start-up, initiation visits and monitoring.
• Ensure safety reporting per protocol and regulatory requirements.
• Coordinate study materials and EC submissions for each site.
• Maintain study documents and trial master files.
• Support budget, contracts, and study payments.

Skills

CRA experience

GCP knowledge

Education

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

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Outlook

Job description

Tigermed is seeking an experienced Clinical Research Associate in Manchester to oversee site management, training, and documentation across trials in line with ICH-GCP and sponsor requirements. You will ensure site initiation, monitoring visits, safety reporting, and study materials coordination, with a strong focus on regulatory compliance and timely issue resolution.

The role demands at least 8 years in CRA roles, a bachelor-level science degree, and proven MS Office skills.