Clinical Development Liaison (Cdl), Spain, Neuromuscular Diseases
hace 2 días
Seville
Clinical Development Liaison (CDL) – Neuromuscular Diseases Business UnitReports to: Program Director, AmplityLocation: Spain (Remote, field‑based)Territory: SpainRole Type: Individual ContributorAbout the RoleAmplity 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 ResponsibilitiesScientific Education & External EngagementEstablish 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‑UpIdentify 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 & EnrollmentPartner 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 CollaborationCoordinate 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 & QualityConduct 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 & ExperienceAdvanced degree in Life Sciences, Pharmacy, Medicine, Nursing, Biomedical Sciences, or a related discipline (MSc, Pharm D, Ph D, 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 autonomously while collaborating effectively in cross‑functional and international teams.Willingness to travel extensively across Spain and occasionally within Europe (approximately 50–70%).Languages: Fluent Spanish and English (written and spoken) are required. Additional European languages are considered an advantage.What We OfferMeaningful Impact– Contribute to the development of innovative therapies that may significantly improve the lives of patients with neuromuscular and rare diseases.Flexibility & Autonomy– Enjoy the benefits of a fully remote, field‑based role, allowing you to manage your territory with a high degree of independence.Professional Growth– Access ongoing training, development opportunities, and exposure to international clinical development programs within a global healthcare organization.Collaborative Culture– Work alongside passionate scientific and clinical experts dedicated to advancing patient care and innovation.Competitive Package– Amplity offers a permanent employment contract, competitive salary, performance‑related incentives, and a comprehensive benefits package.About AmplityAmplity is a global partner of healthcare companies, delivering transformational clinical development and commercialization solutions that improve patient outcomes worldwide.Amplity is an equal opportunity employer. We are committed to creating an inclusive environment where diverse perspectives are valued and empowered. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, disability, marital status, sexual orientation, or veteran status.