Clinical Development Liaison – Neuromuscular Diseases

Amplity Health

. Establish and maintain scientific relationships with KOLs, investigators, study coordinators, and multidisciplinary healthcare teams across the Benelux region .

Posted 9/15/2026full-timeRemote • NetherlandsMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in neuromuscular diseases and clinical research processes, with a strong ability to build relationships with healthcare professionals and stakeholders. Proficient in scientific communication and project management, ensuring compliance and effective collaboration across multidisciplinary teams.

Highest-signal resume keywords

Neuromuscular Diseases ExpertiseClinical Trial SupportScientific Communication SkillsProject Management CapabilitiesFluent English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ProcessesStudy Start-UpSite ManagementPatient RecruitmentStudy ConductInvestigator EngagementCompliance TrainingScientific CollaborationData AnalysisRegulatory Knowledge

Soft Skills

Relationship BuildingInfluencing SkillsOrganizational SkillsAutonomous WorkCross-Functional Collaboration

Industry Keywords

Pharmaceutical IndustryBiotechnologyCROClinical ResearchMedical AffairsClinical Development LiaisonMedical Science LiaisonInvestigator MeetingsPatient AdvocacyHealthcare Institutions

About the role

Key responsibilities & impact

Establish and maintain scientific relationships with KOLs, investigators, study coordinators, and multidisciplinary healthcare teams across the Benelux region
Communicate scientific information about neuromuscular diseases, clinical development programs, pipeline assets, and clinical trials
Support Clinical Advisory Boards, Investigator Meetings, and scientific exchange activities
Represent the organization at national and international congresses, scientific meetings, and educational events
Collaborate with patient advocacy groups and support approved patient engagement initiatives
Identify and assess potential investigators and clinical trial sites across the Netherlands and Belgium
Develop and maintain networks of neuromuscular specialists, referral centers, and clinical research stakeholders
Support site feasibility, study start-up, and investigator engagement strategies
Provide scientific and operational support during site activation and initiation
Partner with investigators and study teams to optimize patient identification and enrollment strategies
Support referral pathways and collaboration among healthcare institutions and specialist centers
Identify recruitment barriers and implement practical solutions
Use disease-area expertise and site insights to maximize recruitment and patient retention
Coordinate interactions among investigators, Clinical Development, Clinical Operations, Medical Affairs, CROs, and internal stakeholders
Gather and communicate field insights to support study execution and strategic decision-making
Provide timely updates following site engagements and investigator interactions
Identify opportunities for scientific collaborations, publications, and Investigator-Initiated Studies
Conduct activities in compliance with applicable laws, regulations, industry codes, and company policies
Complete required compliance and training activities within defined timelines

Requirements

What you’ll need

Advanced degree in Life Sciences, Pharmacy, Medicine, Nursing, Biomedical Sciences, or a related discipline
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 Neuromuscular Diseases and/or Rare Diseases is mandatory
Strong understanding of clinical research processes, including study start-up, site management, patient recruitment, and study conduct
Demonstrated success building long-term relationships with healthcare professionals, investigators, and key external stakeholders
Excellent scientific communication and presentation skills
Strong organizational, influencing, and project management capabilities
Ability to work autonomously while collaborating effectively within cross-functional and international teams
Previous experience in Clinical Development Liaison, Medical Science Liaison, Clinical Operations, Clinical Research, or Medical Affairs roles is highly desirable
Willingness to travel extensively across the Netherlands and Belgium and occasionally within Europe (approximately 50–70%)
Fluent English is required
Fluent Dutch and/or French is strongly preferred
Additional European languages are considered an advantage
Candidates must be based in the Netherlands or Belgium
CV must be submitted in English

Benefits

Comp & perks

Fully remote, field-based role
Ongoing training and development opportunities
Exposure to international clinical development programs
Collaborative culture with scientific and clinical experts
Permanent employment contract
Performance-related incentives
Comprehensive benefits package
Inclusive environment where diverse perspectives are valued and empowered