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Clinical Trial Liaison, Rare Diseases, Paediatric Growth Hormone Deficiency
Amplity Health. Serve as a scientific and operational liaison between clinical trial sites and study teams .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial processes, including patient recruitment, enrollment, and retention strategies, while effectively engaging with stakeholders and maintaining compliance with regulations. Possesses strong communication and organizational skills to facilitate collaboration across clinical operations and research teams.
Highest-signal resume keywords
Clinical Trial ProcessesPatient Recruitment StrategiesGood Clinical Practice (GCP)Stakeholder EngagementClinical Research Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial LiaisonClinical OperationsClinical Research Associate (CRA)Clinical Site ManagementMedical Science Liaison (MSL)Study Start-UpEnrollment InitiativesRegulatory CompliancePediatric EndocrinologyRare Diseases
Soft Skills
Relationship-BuildingCommunication SkillsOrganizational SkillsProject ManagementIndependent Work
Industry Keywords
Clinical ResearchICH GuidelinesStudy ConductHealthcare ProfessionalsReferral Networks
About the role
Key responsibilities & impact- 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 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 to scientific inquiries using approved materials
- Develop relationships with healthcare professionals involved in pediatric endocrine disorders
- Increase awareness of clinical trial opportunities among referral networks and healthcare providers
- Partner with investigators and research teams to optimize patient recruitment strategies
- Assist with patient referral networks and engagement initiatives
- Support recruitment planning and enrollment acceleration activities
- Share best practices across sites to improve recruitment and retention performance
- Collaborate 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 for successful study delivery
- Identify opportunities for future site development and investigator engagement
- Conduct activities in compliance with regulations, GCP, company policies, and industry standards
- Maintain accurate documentation of site interactions and field activities
- Complete required training within designated timelines
- Ensure scientific interactions are compliant, balanced, and evidence based
Requirements
What you’ll need- Bachelor's degree in Life Sciences, Pharmacy, Nursing, Medicine, or another healthcare-related discipline
- Advanced scientific degree (PharmD, MD, MSc, or PhD) preferred
- Previous experience in Clinical Trial Liaison, Clinical Operations, Clinical Research Associate (CRA), Clinical Enrollment, Clinical Site Management, Medical Science Liaison (MSL), or related clinical research roles
- Strong understanding of clinical trial processes including study start-up, recruitment, enrollment, study conduct, and retention
- Experience engaging investigators, study coordinators, healthcare professionals, and research sites
- Knowledge of Good Clinical Practice (GCP), ICH Guidelines, and clinical research regulations
- Demonstrated experience supporting patient recruitment and clinical trial enrollment initiatives
- Experience within Rare Diseases, Pediatric Endocrinology, Endocrinology, Growth Disorders, or related therapeutic areas is strongly preferred
- Experience working within multinational clinical trials is desirable
- Strong stakeholder engagement and relationship-building capabilities
- Ability to work independently while collaborating effectively across global teams
- Excellent communication, organizational, and project management skills
- Fluent English required
- Willingness to travel frequently within the assigned territory
- Domestic and international travel may be required
- Travel requirement approximately 50–70%
- Candidates must be willing and able to travel within their assigned territory as required
- Please submit your CV in English
Benefits
Comp & perks- Field-based role with significant ownership and flexibility
- Ongoing training
- Scientific development opportunities
- Exposure to international clinical development programs
- Competitive salary
- Comprehensive benefits package
- Opportunities for long-term professional growth
- Inclusive environment where diverse perspectives are valued and empowered