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When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose -- moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart(R).
We are seeking a Site Start Up EUCTR II Specialist to join our team in a Hybrid capacity. As a Site Start Up EUCTR II Specialist, you will support the planning and submission of European Union Clinical Trials Regulation (EUCTR) Part II applications for complex, multi-country clinical trials. This position plays a key role in regulatory compliance, clinical trial transparency, and ensuring seamless coordination across multiple stakeholders. You'll collaborate with Clinical Trial Management, Regulatory Affairs, and Clinical Trial Transparency teams to execute submissions that meet EMA requirements via the Clinical Trial Information System (CTIS). Responsibilities include managing country allocations, capturing institutional and investigator information, coordinating document submissions, and monitoring trial milestones, with opportunities to deepen your expertise in regulatory affairs and clinical trial operations.
You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through advancing complex clinical trials across Europe. With diverse teams and continuous learning opportunities, the Site Start Up EUCTR II Specialist can explore career paths and expand skills across clinical research and regulatory operations.
You'll thrive in this role if you bring:
