Clinical Trial Liaison (CTL) Rare Diseases (Paediatric Growth Hormone Deficiency) - India

Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible + specialized medical + commercial services. No matter where a drug is in its lifecycle, we scale with ease to maximize resources + improve impact for all our clients. Through strategic partnerships + deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them. Clinical Trial Liaison (CTL)  Rare Diseases (Paediatric Growth Hormone Deficiency)  Business Unit: Clinical Operations – outsourced through Amplity Reports to: Program Director, Amplity Location: India Territory: India Individual or Manager: Individual Working Model: Field-Based / Remote About the Role:  Amplity is partnering with an innovative biopharmaceutical company focused on developing transformative therapies for patients living with rare diseases.  We are seeking a highly motivated Clinical Trial Liaison (CTL) to support ongoing clinical development programs within Rare Diseases, with a focus on Pediatric Growth Hormone Deficiency (PGHD) and related endocrine disorders.   This field-based role will play a critical part in supporting clinical trial sites, investigator engagement, patient recruitment and retention, referral network development, and overall study execution.  The CTL serves as a key scientific and operational partner to investigators, study coordinators, healthcare professionals, and internal stakeholders, helping to ensure the successful delivery of global clinical development programs.  This is an exciting opportunity to contribute directly to innovative research programs designed to address significant unmet needs for children and families affected by rare endocrine disorders.  Key Responsibilities  Site Relationship Management & Clinical Trial Support  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.  Scientific Education & External Engagement  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.