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Parexel

End-to-end clinical trials and regulatory consulting

Clinical Paediatric Site Engagement Specialist

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree in Life Sciences, Nursing, Pharmacy, Clinical Research, Public Health, or a related discipline.
  • At least 10 years of relevant clinical research experience, or an equivalent combination of education and experience.
  • Demonstrated experience supporting paediatric clinical trials, paediatric research sites, or paediatric investigator networks.
  • Experience working directly with investigators and clinical trial sites.
  • Experience supporting site identification, feasibility, startup, recruitment, and enrolment activities.
  • Established relationships with children's hospitals, paediatric neurology programs, paediatric headache centres, or paediatric research institutions across Europe.
  • Strong communication, organization, and problem-solving skills.
  • Willingness and ability to travel extensively throughout Europe, with a minimum of 50% travel.

Responsibilities

  • Identify and evaluate new paediatric migraine clinical research sites across Europe.
  • Build and maintain relationships with paediatric investigators, children's hospitals, paediatric headache centres, and study site personnel.
  • Support site feasibility assessments, startup activities, site activation, and enrolment initiatives.
  • Identify and address barriers to participant recruitment, enrolment, and retention.
  • Support intervention and recovery efforts for underperforming study sites.
  • Gather investigator feedback and site intelligence to inform study execution and recruitment strategies.
  • Partner with study teams to prioritize opportunities and mitigate enrolment risks.
  • Conduct frequent in-person site visits and investigator engagements throughout Europe.

Desired Qualifications

  • An advanced degree (MS, MPH, PharmD, MD, PhD, NP, PA, or equivalent).
  • 5–7+ years of experience in paediatric clinical development, paediatric neurology, migraine, neuroscience, or paediatric clinical research.
  • An existing network of paediatric 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, enrolment acceleration, and site rescue activities.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

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.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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