## Clinical Trial Liaison (CTL)
- Rare Diseases (Paediatric Growth Hormone Deficiency)
- Argentina/ColombiaApply: Colombia: Argentina: Full time: Posted Today: R6281Join 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 AmplityReports to: Program Director, Amplity

Location:
ArgentinaTerritory: Argentina & ColombiaIndividual or Manager: IndividualWorking 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 integral 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.




* Increase awareness of clinical trial opportunities among referral networks and appropriate healthcare providers. Clinical Trial Recruitment & Enrollment
* 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. Cross-Functional Collaboration
* 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. Compliance
* Conduct all activities in compliance with applicable regulations, Good Clinical Practice (GCP), 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. Required Qualifications & Experience
* 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 res

📌 Clinical Trial Liaison (Argentina)
🏢 Amplity
📍 Argentina