Parexel
Pediatric Site Engagement Specialist - FSP
United Kingdom · Work style not stated
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About the role
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- EmployerParexel
- LocationUnited Kingdom
- Work styleWork style not stated
- Employer posted
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.
Show full description
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.
Key Responsibilities
- Identify and evaluate new pediatric migraine study sites across Europe.
- Build and maintain relationships with pediatric investigators, children's hospitals, pediatric headache centers, and study site personnel.
- Support site feasibility, startup, activation, and enrollment activities.
- Identify and address barriers to recruitment, enrollment, and participant retention.
- Support rescue activities for underperforming sites.
- Gather investigator feedback and site intelligence to inform study execution and recruitment strategy.
- Partner with study teams to prioritize opportunities and mitigate enrollment risks.
- Conduct frequent in-person site visits and investigator engagements throughout Europe.
Required Qualifications
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, Clinical Research, Public Health, or related discipline.
- Minimum 10 years of relevant clinical research experience, or equivalent combination of education and experience.
- Demonstrated experience supporting pediatric clinical trials, pediatric research sites, or pediatric investigator networks.
- Experience working directly with investigators and clinical trial sites.
- Experience supporting site identification, feasibility, startup, recruitment, and enrollment activities.
- Established relationships with children's hospitals, pediatric neurology programs, pediatric headache centers, or pediatric research institutions across Europe.
- Strong communication, networking, and relationship-building skills.
- Willingness and ability to travel extensively throughout Europe (minimum 50% travel).
Preferred Qualifications
- Advanced degree (MS, MPH, PharmD, MD, PhD, NP, PA, or equivalent).
- 5-7+ years of experience in pediatric clinical development, pediatric neurology, migraine, neuroscience, or pediatric clinical research.
- Existing network of pediatric investigators and research coordinators across Europe.
- Prior experience as a CRA, Site Care Partner, Clinical Trial Manager, Study Manager, Clinician, or Clinical Operations professional.
- Experience supporting multi-country European clinical trials and working across multiple European healthcare systems.
- Experience in recruitment recovery, enrollment acceleration, and site rescue activities.
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At a glance
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