CRA II: Oncology Site Monitoring & Trial Oversight

IQVIA; Reading; On-site; GBP 42,000 - 70,000; Full time

Job summary

IQVIA Biotech is seeking a dedicated On-site Monitor to support oncology trials in the UK. You will conduct site visits, ensure protocol and regulatory compliance, and coordinate with study teams to drive enrollment and data integrity.

You will train site personnel on study procedures, track progress, and maintain essential TMF/ISF documentation while collaborating with cross-functional groups to meet project objectives in a fast-paced environment.

Qualifications

• 1 year+ of on-site monitoring experience in clinical trials.
• Experience monitoring Oncology studies is essential.
• Bachelor’s degree in science or health care field or equivalent.
• Familiarity with GCP and ICH guidelines and regulatory practice.
• Strong written and verbal English communication skills.
• Proficient in MS Word, Excel and PowerPoint; able to manage documentation.
• Able to manage time and finances and work with study teams.

Responsibilities

• Perform site monitoring visits in line with GCP/ICH and contract scope.
• Collaborate with sites to recruit and monitor subject enrollment as required.
• Administer protocol training and maintain regular site communications.
• Assess site practices for protocol compliance and regulatory adherence.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Maintain Trial Master File and Investigator Site File documentation.
• Prepare visit reports, follow-up letters, and study documentation.
• Coordinate with study team for project execution support.

Skills

On-site monitoring experience

Oncology study monitoring

English language proficiency

Analytical and problem-solving skills

Time and financial management

Communication skills

MS Word/Excel/PowerPoint proficiency

Education

Bachelor's Degree in scientific discipline or health care

Equivalent combination of education, training and experience

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Laptop computer

iPhone

iPad

Job description

IQVIA Biotech is seeking a dedicated On-site Monitor to support oncology trials in the UK. You will conduct site visits, ensure protocol and regulatory compliance, and coordinate with study teams to drive enrollment and data integrity.

You will train site personnel on study procedures, track progress, and maintain essential TMF/ISF documentation while collaborating with cross-functional groups to meet project objectives in a fast-paced environment.