Senior CRA – Site Management & Study Start-Up

Tigermed; Basildon; On-site; GBP 35,000 - 52,000; Full time

Job summary

Tigermed is seeking a Clinical Research Associate to oversee site management, initiate studies, monitor progress and ensure compliance with ICH-GCP. You will coordinate study materials and communicate with Principal Investigators across sites in the UK.

The role requires a bachelor degree in medical/biological fields, 8+ years CRA experience, strong knowledge of GCP and trial operations, and proficiency with MS Word, Excel, PowerPoint and Outlook.

Qualifications

• Bachelor degree or above in Medical, Pharmacology or Biology related major.
• At least 8 years CRA experience.
• Good understanding of ICH-GCP and trial operation processes.
• Proficient in Microsoft Word, Excel, PPT and Outlook.

Responsibilities

• Site management including SIV, initiation, and monitoring.
• Provide training on ICH-GCP and protocol requirements.
• Maintain essential documents and trial master file.
• Ensure safety reporting and SAE timelines.
• Manage budgets and study payments.
• Update and maintain study tools and systems.

Skills

CRA experience 8+ years

GCP knowledge

Study monitoring

Education

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

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Outlook

Job description

Tigermed is seeking a Clinical Research Associate to oversee site management, initiate studies, monitor progress and ensure compliance with ICH-GCP. You will coordinate study materials and communicate with Principal Investigators across sites in the UK.

The role requires a bachelor degree in medical/biological fields, 8+ years CRA experience, strong knowledge of GCP and trial operations, and proficiency with MS Word, Excel, PowerPoint and Outlook.