Oncology CRA II: Frontline Site Monitoring in Biotech

IQVIA LLC; Leeds; On-site; GBP 45,000 - 65,000; Full time

Job summary

IQVIA Biotech in Leeds is seeking an experienced Clinical Research Associate to perform on-site monitoring visits for oncology trials, ensuring GCP/ICH compliance and proper trial conduct. You will manage site communications, training, and documentation, while supporting recruitment plans and study start-up activities.

The role requires 1 year of on-site monitoring experience, strong English communication, and solid organizational and financial management skills.

Qualifications

• Bachelor's Degree in scientific discipline or health care preferred.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Basic knowledge of Good Clinical Practice (GCP) and ICH guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Responsibilities

• Perform site monitoring visits in accordance with GCP/ICH and contracted scope.
• Drive and track subject recruitment plan to enhance predictability.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site practices for protocol adherence and regulatory compliance.
• Track regulatory submissions, recruitment, CRF completion and data query resolution.
• Ensure site documents are filed in TMF and ISF maintained per regulations.
• Create and maintain site management documentation and visit reports.
• Collaborate with study team for project execution support.
• May support start-up phase and site financial management as applicable.

Skills

GCP compliance

ICH guidelines

On-site monitoring

English communication

Time management

Financial management

Team collaboration

Education

Bachelor's degree in scientific discipline or health care

Tools

Microsoft Word

Excel

PowerPoint

Laptop

iPhone

iPad

Job description

IQVIA Biotech in Leeds is seeking an experienced Clinical Research Associate to perform on-site monitoring visits for oncology trials, ensuring GCP/ICH compliance and proper trial conduct. You will manage site communications, training, and documentation, while supporting recruitment plans and study start-up activities.

The role requires 1 year of on-site monitoring experience, strong English communication, and solid organizational and financial management skills.