IQVIA is seeking an experienced Clinical Research Associate in Manchester to monitor interventional studies in line with GCP and ICH guidelines. You will manage site visits, training, and communications with investigative sites to ensure protocol adherence and data quality.
The role requires at least 2 years on-site monitoring experience, a degree in a scientific or health care field, and strong knowledge of regulatory requirements.
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CRA II — On‑Site Monitoring & Study Oversight in Manchester employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
