Clinical Paediatric Site Engagement Specialist
Parexel
Clinical Paediatric Site Engagement Specialist
Parexel
End-to-end clinical trials and regulatory consulting
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.
About Parexel
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®.
About the Role
We are seeking a Clinical Paediatric Site Engagement Specialist (Paediatric Clinical Research Engagement Specialist, Paediatric Site Partnerships Specialist) to join our team in a remote capacity in the UK or Belgium.
As a Clinical Paediatric Site Engagement Specialist, you will play a critical role in advancing paediatric migraine research across Europe by strengthening relationships with investigators and clinical research sites, accelerating site activation and enrolment, and supporting successful study execution.
This position is central to improving recruitment performance, enhancing investigator engagement, and helping bring innovative therapies to paediatric patients through high-quality clinical research. Responsibilities include site identification and evaluation, investigator and site engagement, support for feasibility and startup activities, recruitment and enrolment optimization, and the collection of site intelligence to inform study strategy. You will have the opportunity to make a meaningful impact on study outcomes while partnering with experienced clinical development and operations teams.
You’ll join a fast-paced, growth-oriented environment focused on improving site performance, accelerating patient enrolment, and supporting successful execution of the Paediatric Migraine Program. With diverse teams and continuous learning opportunities, the Clinical Paediatric Site Engagement Specialist can expand expertise across paediatric clinical development, site engagement strategy, and clinical operations while contributing to research that has the potential to improve the lives of children living with migraine.
Key Responsibilities
Candidate Profile
You’ll thrive in this role if you bring:
Required Qualifications
Preferred Qualifications
Benefits and Compensation
We offer a comprehensive benefits package to eligible employees, which includes life assurance, medical and dental insurance, and additional benefit offerings in accordance with the terms of our applicable plans.
If this job doesn’t sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, send them the link to apply!
We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.
Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.
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