Senior Clinical Research Associate (CRA) - UK

Iqvia Cfsp; Bracknell; On-site; GBP 32,000 - 46,000; Full time

Benefits offered by this job

World-class training

Professional development

Career advancement opportunities

Job summary

IQVIA cFSP is seeking experienced Clinical Research Associates in the United Kingdom to perform site monitoring visits in accordance with GCP and ICH guidelines. You will work with sites to drive subject recruitment, administer protocol training, and ensure timely, compliant data collection.

Travel to sites is required, and you will track regulatory submissions and data queries while maintaining site documentation.

Qualifications

• Minimum 18 months of independent on-site monitoring.
• Experience managing multiple trials across diverse investigative sites.
• Strong knowledge of GCP and ICH guidelines.
• Life science degree or equivalent industry experience.
• Willingness to travel to study sites.

Responsibilities

• Conduct site monitoring visits per contracted scope and regulatory requirements.
• Collaborate with sites to recruit and enroll subjects per project needs.
• Provide protocol and study training to assigned sites and maintain communication.
• Assess quality of site practices and escalate issues as needed.
• Track regulatory submissions, approvals, enrollment, CRF completion and data queries.
• Maintain TMF/ISF documentation and visit reports.
• Collaborate with study team for project execution.

Skills

On-site monitoring

Protocol management

GCP knowledge

ICH knowledge

Travel flexibility

Education

Life science degree

Job description

IQVIA cFSP is seeking experienced Clinical Research Associates in the United Kingdom to perform site monitoring visits in accordance with GCP and ICH guidelines. You will work with sites to drive subject recruitment, administer protocol training, and ensure timely, compliant data collection.

Travel to sites is required, and you will track regulatory submissions and data queries while maintaining site documentation.