Clinical Trial Liaison, Rare Diseases, Paediatric Growth Hormone Deficiency

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🔥 1 hour ago

🌐 Argentina, Colombia – Remote

🇦🇷 Argentina – Remote 🇨🇴 Colombia – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

📈 Growth Marketing

👻 Ghost score 10%

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Amplity Health

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

Amplity Health is a global contract sales and commercial organization partnering with pharmaceutical and biotechnology companies to provide tailored outsourced programs and communications throughout a drug's life cycle. They specialize in scientific stakeholder engagement and go-to-market strategies by emphasizing person-to-person interactions with physicians, patients, payers, community organizations, and life science executives. Amplity manages and employs stakeholder-facing professionals globally to ensure that more patients gain access to the best medicines. Their expertise includes oncology, rare diseases, and specialty therapies, with a focus on precision medicine solutions. Amplity's services extend to medical communications, market access, commercial sales, and providing real-time insights through proprietary AI-powered technology to enhance stakeholder engagement.

📋 Description

• 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

• 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

• 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

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