Parexel is seeking a Clinical Research Associate (CRA) to manage investigator sites throughout the lifecycle of assigned clinical trials. You will monitor, support site activation, ongoing study conduct, and close-out while safeguarding patient safety and data integrity.
You will collaborate with the Site Care Partner and study team to ensure protocol compliance, site performance and timely delivery of study milestones. Travel will be substantial, with remote monitoring as needed.
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Clinical Research Associate: Site Monitoring Oversight in Dover employer: PAREXEL
At Parexel, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. Our team members enjoy competitive benefits, including flexible working arrangements and opportunities for career advancement, all while contributing to impactful global clinical trials in a supportive environment across the UK, Poland, Serbia, and Hungary.
