Remote CRA — Real-World Evidence Monitoring (Phase 3/4)

IQVIA; Reading; Remote; GBP 30,000 - 50,000; Full time

Job summary

A leading clinical research organization in the UK is seeking a Clinical Research Associate (CRA I OR CRA II) to conduct monitoring visits for Phase 3b and Phase 4 studies. Candidates should have independent monitoring experience, knowledge of GCP and ICH guidelines, and the ability to travel to sites across the UK and Ireland. This position offers work flexibility and opportunities for career development.

Benefits

Career development opportunities

Work on cutting-edge medicines

Qualifications

• Minimum 6 months of independent on-site monitoring experience.
• Successfully managed multiple clinical trial protocols.
• In-depth knowledge of GCP and ICH guidelines.

Responsibilities

• Perform site monitoring visits in compliance with regulations.
• Adapt and track subject recruitment plans as needed.
• Administer study training to assigned sites.
• Evaluate site practices for protocol adherence.
• Manage the progress of assigned studies.
• Ensure site documents are properly filed.
• Create and maintain documentation regarding site management.
• Collaborate with study team members for project support.

Skills

Independent on-site monitoring

Project management

Knowledge of GCP and ICH guidelines

Flexibility to travel

Education

Life science degree or equivalent industry experience

Job description

A leading clinical research organization in the UK is seeking a Clinical Research Associate (CRA I OR CRA II) to conduct monitoring visits for Phase 3b and Phase 4 studies. Candidates should have independent monitoring experience, knowledge of GCP and ICH guidelines, and the ability to travel to sites across the UK and Ireland. This position offers work flexibility and opportunities for career development.