Parexel seeks a Site Activation Partner for a 6-month temporary assignment to advance clinical research through site activation and start-up activities. You will manage essential documents, regulatory submissions, and study systems while collaborating with investigator sites, regulatory stakeholders, and cross-functional teams.
Ideal candidates bring 2+ years in site activation, familiarity with CTMS/eTMF/eISF, and strong organizational skills to support on-time study delivery in a regulated
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Contract Site Activation Specialist in Uxbridge 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.
