Parexel is seeking a Senior Clinical Study Administrator to join our UK team. The role focuses on coordinating and administering clinical studies from start-up through to close-out, ensuring quality and timely delivery.
You will be the local contact, supporting CRAs and trial managers across systems like CTMS and eTMF. The position requires a degree, strong organizational skills, IT proficiency, and fluency in English and French.
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Senior Clinical Study Administrator - Luton On-Site 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.
