Senior CRA, Oncology — Fast-Paced Biotech Impact
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Research/Development
Research Scientist, Regulatory Compliance Specialist
Job Description & How to Apply Below
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.
We are currently recruiting a Senior CRA, Oncology — Fast-Paced Biotech Impact for our team in England, United Kingdom.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior CRA, Oncology — Fast-Paced Biotech Impact role in the description above.
We appreciate your interest in this position.
Join IQVIA Inc and contribute to our ongoing work.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).