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Amplity

Global contract services for drug lifecycle

Clinical Trial Liaison - Rare Diseases, Paediatric Growth Hormone Deficiency

Clinical Research OperationsPosted on Nov 9
Full-timeNo salary listedRemote

About the Job

Requirements

  • A bachelor's degree in Life Sciences, Pharmacy, Nursing, Medicine, or another healthcare-related discipline is required.
  • Previous experience in Clinical Trial Liaison, Clinical Operations, Clinical Research Associate, Clinical Enrollment, Clinical Site Management, Medical Science Liaison, or related clinical research roles is required.
  • A strong understanding of clinical trial processes, including study start-up, recruitment, enrollment, study conduct, and retention, is required.
  • Experience engaging investigators, study coordinators, healthcare professionals, and research sites is required.
  • Knowledge of Good Clinical Practice, ICH Guidelines, and clinical research regulations is required.
  • Demonstrated experience supporting patient recruitment and clinical trial enrollment initiatives is required.
  • Strong stakeholder engagement and relationship-building capabilities are required.
  • Ability to work independently while collaborating effectively across global teams is required.
  • Excellent communication, organizational, and project management skills are required.
  • Fluent English is required.
  • Willingness to travel frequently within the assigned territory is required; approximately 50–70% travel, including domestic and international travel, may be required.
  • Candidates must be willing and able to travel within their assigned territory as required.

Responsibilities

  • Serve as a scientific and operational liaison between clinical trial sites and study teams.
  • Support study start-up, site activation, patient recruitment, enrollment, and retention activities.
  • Build and maintain strong relationships with investigators, study coordinators, referral centers, and research staff.
  • Support sites in identifying and addressing recruitment barriers and enrollment challenges.
  • Assist sites with patient identification strategies and referral pathway development.
  • Coordinate site-facing activities with Clinical Operations, CROs, and internal stakeholders.
  • Support achievement of study enrollment objectives and clinical milestones.
  • Provide accurate, non-promotional scientific information regarding disease state, study rationale, trial protocols, and patient eligibility criteria.
  • Support investigator meetings, educational events, and scientific exchanges.
  • Respond appropriately to scientific inquiries from investigators and site personnel using approved materials.
  • Develop strong relationships with healthcare professionals involved in the diagnosis and management of pediatric endocrine disorders.
  • Increase awareness of clinical trial opportunities among referral networks and appropriate healthcare providers.
  • Partner with investigators and research teams to optimize patient recruitment strategies.
  • Assist sites with the development of patient referral networks and engagement initiatives.
  • Support recruitment planning and enrollment acceleration activities.
  • Share best practices across sites to improve recruitment and retention performance.
  • Work closely with Clinical Development, Clinical Operations, Medical Affairs, and CRO partners.
  • Gather actionable insights from sites and investigators and communicate them to internal stakeholders.
  • Support scientific training activities for study personnel.
  • Facilitate alignment among internal and external stakeholders to ensure successful study delivery.
  • Identify opportunities for future site development and investigator engagement.
  • Conduct all activities in compliance with applicable regulations, Good Clinical Practice, company policies, and industry standards.
  • Maintain accurate documentation of site interactions and field activities.
  • Complete required training within designated timelines.
  • Ensure all scientific interactions are compliant, balanced, and evidence based.

Desired Qualifications

  • An advanced scientific degree (PharmD, MD, MSc, or PhD) is preferred.
  • Experience within Rare Diseases, Pediatric Endocrinology, Endocrinology, Growth Disorders, or related therapeutic areas is strongly preferred.
  • Experience working within multinational clinical trials is desirable.
  • Additional local languages are advantageous.
  • Experience supporting clinical trials, patient recruitment, site engagement, or clinical operations activities is highly desirable.
  • Experience in Rare Diseases, Pediatric Endocrinology, Endocrinology, Growth Disorders, or related therapeutic areas is strongly preferred.

About the Company

Amplity

Global contract services for drug lifecycle

Amplity Health is a global contract organization delivering medical and commercial services to pharmaceutical and healthcare companies across the full drug lifecycle—from development to launch and beyond. It uses an AI-driven platform and a HIPAA-compliant database to provide actionable insights that help clients make decisions during the drug launch window, and it offers contract Medical Science Liaisons and patient support teams to engage healthcare providers and patients. Its services are contract-based and scalable, enabling clients to adjust medical and commercial operations as a product progresses. By combining data-driven insights, hands-on medical affairs execution, and a flexible workforce, Amplity aims to accelerate drug approvals, commercialization, and market access while ensuring compliant data handling.

Company size
1-10
Company stage
Debt Financing
Total funding
$102.5M
Headquarters
Santa Cruz, CA
Founded
2010

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