Clinical Development Liaison

Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible + specialized medical + commercial services. No matter where a drug is in its lifecycle, we scale with ease to maximize resources + improve impact for all our clients. Through strategic partnerships + deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them.

Clinical Development Liaison (CLD) - Neuromuscular Diseases - Benelux

Business Unit: Clinical Development & Operations

Reports to: Program Director, Amplity

Location: Netherlands or Belgium (Remote)

Territory: Benelux (Netherlands & Belgium)

About The Role

Amplity is partnering with a leading biotechnology company focused on developing innovative therapies for patients living with severe neuromuscular diseases.

We are seeking a highly motivated Clinical Development Liaison (CDL) to support clinical development activities across the Benelux region, with a primary focus on the Netherlands and Belgium. This field-based scientific role will play a critical part in supporting clinical trial start-up, investigator engagement, patient identification, recruitment strategies, and study execution.

The CDL serves as a key scientific bridge between investigators, healthcare professionals, clinical sites, and internal stakeholders, helping to accelerate the successful delivery of clinical studies in rare and neuromuscular disorders.

Working closely with Medical Affairs, Clinical Development, Clinical Operations, CRO partners, and international colleagues, the CDL will help build strong scientific relationships and support high-quality study conduct throughout the clinical trial lifecycle.

This role offers a unique opportunity to contribute to pioneering research that has the potential to transform the lives of patients living with rare and often underserved neuromuscular diseases.

Key Accountabilities

Scientific Education & External Engagement

• Establish and maintain trusted scientific relationships with Key Opinion Leaders (KOLs), investigators, study coordinators, and multidisciplinary healthcare teams throughout the Benelux region.
• 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 organization 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 the Netherlands and Belgium.
• 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 and specialist centers.
• Facilitate discussions with sites to identify barriers to recruitment and implement practical 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, Medi