Clinical Trial Liaison, Rare Diseases, Paediatric Growth Hormone Deficiency

This is a fully remote position, open to applicants in Argentina, +1 more country.

📋 Description

• Act as a scientific and operational intermediary between clinical trial sites and study teams.

• Facilitate study initiation, site activation, patient recruitment, enrollment, and retention efforts.

• Establish and nurture relationships with investigators, study coordinators, referral centers, and research personnel.

• Assist sites in recognizing and overcoming recruitment obstacles and enrollment difficulties.

• Aid sites with strategies for patient identification and the development of referral pathways.

• Coordinate site-related activities with Clinical Operations, CROs, and internal stakeholders.

• Contribute to the achievement of study enrollment targets and clinical milestones.

• Provide precise, non-promotional scientific information regarding the disease state, study rationale, trial protocols, and patient eligibility criteria.

• Support investigator meetings, educational events, and scientific discussions.

• Address scientific inquiries using approved materials.

• Cultivate relationships with healthcare providers involved in pediatric endocrine disorders.

• Enhance awareness of clinical trial opportunities within referral networks and healthcare professionals.

• Collaborate with investigators and research teams to refine patient recruitment strategies.

• Assist with patient referral networks and engagement initiatives.

• Facilitate recruitment planning and activities aimed at accelerating enrollment.

• Share best practices across sites to enhance recruitment and retention outcomes.

• Work together with Clinical Development, Clinical Operations, Medical Affairs, and CRO partners.

• Collect actionable insights from sites and investigators and relay them to internal stakeholders.

• Support scientific training initiatives for study personnel.

• Foster alignment among internal and external stakeholders to ensure successful study execution.

• Identify prospects for future site development and investigator involvement.

• Conduct activities in accordance with regulations, GCP, company policies, and industry standards.

• Maintain thorough documentation of site interactions and field activities.

• Complete mandatory training within specified timelines.

• Ensure scientific interactions adhere to compliance, balance, and evidence-based standards.

⛳️ Requirements

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, Medicine, or another healthcare-related field.

• An advanced scientific degree (PharmD, MD, MSc, or PhD) is preferred.

• Prior experience in roles such as Clinical Trial Liaison, Clinical Operations, Clinical Research Associate (CRA), Clinical Enrollment, Clinical Site Management, Medical Science Liaison (MSL), or related clinical research positions.

• Strong comprehension of clinical trial processes, including study initiation, recruitment, enrollment, study conduct, and retention.

• Experience in engaging with investigators, study coordinators, healthcare professionals, and research sites.

• Familiarity with Good Clinical Practice (GCP), ICH Guidelines, and clinical research regulations.

• Proven track record in supporting patient recruitment and clinical trial enrollment efforts.

• Experience in Rare Diseases, Pediatric Endocrinology, Endocrinology, Growth Disorders, or related therapeutic fields is highly preferred.

• Experience in multinational clinical trials is advantageous.

• Strong skills in stakeholder engagement and relationship-building.

• Capable of working independently while effectively collaborating across global teams.

• Exceptional communication, organizational, and project management abilities.

• Proficiency in English is required.

• Willingness to travel frequently within the designated territory.

• Domestic and international travel may be necessary.

• Travel commitment of approximately 50–70%.

• Candidates must be prepared and able to travel within their assigned territory as required.

• Please submit your CV in English.

🏝️ Benefits

• Field-based position with substantial ownership and flexibility.

• Continuous training opportunities.

• Scientific development prospects.

• Exposure to international clinical development initiatives.

• Competitive compensation package.

• Comprehensive benefits offerings.

• Opportunities for long-term professional advancement.

• Inclusive environment that values and empowers diverse perspectives.