Clinical Development Liaison; CDL Neuromuscular Diseases

Puesto: Clinical Development Liaison (CDL Neuromuscular Diseases
Location: Puerto Rico

Clinical Development Liaison (CDL) – Neuromuscular Diseases Business Unit

Reports to:

Program Director, Amplity

Location:

Spain (Remote, field‑based)
Territory:
Spain
Role Type:
Individual Contributor
About the Role  Amplity is partnering with a leading biopharmaceutical company committed to advancing innovative therapies for patients living with neuromuscular diseases. The CDL will support clinical development activities across Spain, focusing on study start‑up, investigator engagement, patient identification, recruitment strategies, and study execution. The role serves as a scientific bridge between investigators, healthcare professionals, clinical sites, and internal stakeholders to accelerate successful delivery of clinical studies in rare and neuromuscular disorders.

Key Responsibilities  Scientific Education & External Engagement   Establish and maintain trusted scientific relationships with Key Opinion Leaders (KOLs), investigators, study coordinators, and multidisciplinary healthcare teams.
Communicate scientific information related to neuromuscular diseases, clinical development programs, pipeline assets, and ongoing clinical trials.
Support the planning and execution of Clinical Advisory Boards, Investigator Meetings, and scientific exchange activities.
Represent the company at national and international congresses, scientific meetings, and educational events.
Collaborate with patient advocacy groups and support approved patient engagement initiatives.
Act as a scientific ambassador for the organization, strengthening awareness and engagement within the neuromuscular community.
Clinical Trial Start‑Up   Identify and assess potential investigators and clinical trial sites across Spain.
Develop and maintain a strong network of neuromuscular specialists, referral centers, and clinical research stakeholders.
Support site feasibility, study start‑up activities, and investigator engagement strategies.
Provide scientific and operational support to study sites during activation and initiation phases.
Patient Recruitment & Enrollment   Partner with investigators and study teams to optimize patient identification and enrollment strategies.
Support the development of referral pathways and collaboration among healthcare institutions.
Facilitate discussions with sites to identify barriers to recruitment and implement solutions.
Leverage disease‑area expertise and site insights to maximize recruitment performance and patient retention.
Study Conduct & Cross‑Functional Collaboration   Coordinate interactions among investigators, Clinical Development, Clinical Operations, Medical Affairs, CROs, and other internal stakeholders.
Gather and communicate actionable field insights to support study execution and strategic decision‑making.
Provide timely updates following site engagements and investigator interactions.
Identify opportunities related to scientific collaborations, publications, and Investigator‑Initiated Studies (IIS/IITs), ensuring appropriate internal alignment.
Compliance & Quality   Conduct all activities in compliance with applicable laws, regulations, industry codes, and company policies.
Maintain the highest ethical and scientific standards in all stakeholder interactions.
Complete all required compliance and training activities within defined timelines.

Required Qualifications & Experience   Advanced degree in Life Sciences, Pharmacy, Medicine, Nursing, Biomedical Sciences, or a related discipline (MSc, PharmD, PhD, or MD preferred).
Minimum of 5 years of experience within the pharmaceutical, biotechnology, CRO, or clinical research industry.
Previous experience supporting clinical trials and engaging with investigators and healthcare professionals.
Experience in Neurology, Neuromuscular Diseases, Rare Diseases, or Neuroscience is mandatory.
Strong understanding of clinical research processes, including study start‑up, site management, and patient recruitment.
Demonstrated success building long‑term relationships with healthcare professionals and key external stakeholders.
Excellent scientific communication and presentation skills.
Strong organizational and project management capabilities.
Ability to work…