Senior Contractor CRA – UK: Site & Safety Lead

Tigermed; Woking; On-site; GBP 50,000 - 70,000; Full time

Job summary

Tigermed is seeking an experienced Clinical Research Associate to manage study sites, initiate and monitor studies in accordance with protocol and regulatory requirements. You will coordinate safety reporting, budgeting and contract processes, and maintain essential study documentation across multiple sites.

The ideal candidate has a Bachelor degree in a medical-related field and at least 8 years of CRA experience, with strong knowledge of ICH-GCP and trial operations, plus proficiency in Word,

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 initiation (SIV) and clinical monitoring.
• Ensure safety reporting requirements and SAE timelines are met.
• Finalize budget and contracts prior to site initiation.
• Update and maintain Study tools and systems in a timely manner.

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 to manage study sites, initiate and monitor studies in accordance with protocol and regulatory requirements. You will coordinate safety reporting, budgeting and contract processes, and maintain essential study documentation across multiple sites.

The ideal candidate has a Bachelor degree in a medical-related field and at least 8 years of CRA experience, with strong knowledge of ICH-GCP and trial operations, plus proficiency in Word,