Oncology Clinical Research Associate - Site Monitoring Pro

IQVIA LLC; Pudsey; Vor Ort; GBP 32.000 - 52.000; Vollzeit

Zusammenfassung

IQVIA Biotech in the United Kingdom is seeking a Clinical Research Associate to perform on-site monitoring visits for oncology studies. You will ensure GCP/ICH compliance, manage site communications, and track recruitment and data quality to support trial progress.

Collaborating with study teams, you will prepare visit reports, resolve issues, and help maintain trial master file integrity. A background in life sciences, strong English communication, and solid organizational skills are essential;

Qualifikationen

• Minimum 1 year of on-site monitoring experience.
• Experience monitoring oncology studies is essential.
• Bachelor's degree in a scientific discipline or healthcare preferred.
• GCP/ICH regulatory knowledge and practice.
• Proficient with MS Office and basic mobile devices.
• Strong written and spoken English communication.
• Excellent organizational and problem-solving abilities.
• Ability to work with study sponsors and sites.

Aufgaben

• Perform site monitoring visits per contracted scope and GCP/ICH guidelines.
• Collaborate with sites to adapt and track subject recruitment plans.
• Administer protocol training and maintain regular site communications.
• Evaluate site practices for protocol compliance and data integrity.
• Track regulatory submissions, enrollment, CRF completion, and data queries.
• May support start-up activities as needed.
• Maintain TMF/ISF documentation and conduct visit reporting.
• Prepare follow-up letters and other required study documents.
• Coordinate with the study team for project execution support.
• Support site-level recruitment plans and, if applicable, invoicing.

Kenntnisse

On-site monitoring

Oncology studies

GCP/ICH knowledge

English communication

Organizational skills

Time management

Team collaboration

Regulatory submissions tracking

Ausbildung

Bachelor's degree in science or healthcare

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Jobbeschreibung

IQVIA Biotech in the United Kingdom is seeking a Clinical Research Associate to perform on-site monitoring visits for oncology studies. You will ensure GCP/ICH compliance, manage site communications, and track recruitment and data quality to support trial progress.

Collaborating with study teams, you will prepare visit reports, resolve issues, and help maintain trial master file integrity. A background in life sciences, strong English communication, and solid organizational skills are essential;