Senior CRA, Oncology — Fast-Paced Biotech Impact

IQVIA Inc

England

On-site

GBP 42,000 - 64,000

Full time

6 days ago

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Job summary

IQVIA Biotech seeks an on-site Clinical Research Monitor with oncology study experience to oversee site performance, protocol adherence, and data quality across trials in the United Kingdom. You will collaborate with investigative sites, manage recruitment plans, and ensure regulatory compliance throughout the study lifecycle.

The role requires a science/healthcare background, strong English communication, and proficiency with standard MS Office tools.

Qualifications

Minimum 1 year of on-site monitoring experience.
Experience monitoring Oncology studies is required.
Bachelor’s degree in a scientific discipline or healthcare preferred.
Equivalents accepted in lieu of degree.
Knowledge of GCP/ICH guidelines at a basic level.
Strong communication in English; good writing and presentation skills.

Responsibilities

Perform site monitoring visits per scope and regulatory requirements (GCP/ICH).
Collaborate with sites to recruit subjects and track recruitment plans.
Train sites on protocol and study procedures; maintain regular communication.
Assess site practices for protocol compliance and regulatory adherence.
Monitor study progress: regulatory submissions, recruitment, CRF completion, data queries; support start-up if needed.
Maintain site documentation and Trial Master File from visit notes and follow-ups.