Senior CRA - Sponsor-Dedicated Clinical Monitoring (UK)

IQVIA; Livingston; On-site; GBP 30,000 - GBP 45,000; Full time

Job summary

A leading global provider of clinical research services in Scotland is seeking a Clinical Research Associate. The role involves monitoring sites, ensuring compliance with study protocols and regulations, and documenting site management activities. Candidates should have a Bachelor's degree in a scientific discipline, relevant on-site monitoring experience, and strong communication skills. This is a full-time position and not eligible for UK visa sponsorship.

Qualifications

• Minimum 1 year of on-site monitoring experience required.
• Bachelor's degree in a scientific discipline or health care preferred.
• Good knowledge of clinical research regulatory requirements.

Responsibilities

• Perform site monitoring visits as per Good Clinical Practice.
• Evaluate quality and integrity of study site practices.
• Manage progress of assigned studies and ensure document filing.

Skills

On-site monitoring experience

Knowledge of GCP and ICH guidelines

Microsoft Office proficiency

Organizational skills

Effective communication

Education

Bachelor's Degree in scientific discipline or health care

Job description

A leading global provider of clinical research services in Scotland is seeking a Clinical Research Associate. The role involves monitoring sites, ensuring compliance with study protocols and regulations, and documenting site management activities. Candidates should have a Bachelor's degree in a scientific discipline, relevant on-site monitoring experience, and strong communication skills. This is a full-time position and not eligible for UK visa sponsorship.