Clinical development liaison (cld) - neuromuscular diseases - benelux

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.

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.
• Clinical Trial Start-Up: Identify and assess potential investigators and clinical trial sites across the Netherlands and Belgium.
• Patient Recruitment & Enrollment: Partner with investigators and study teams to optimize patient identification and enrollment strategies.
• Study Conduct & Cross-Functional Collaboration: Coordinate interactions among investigators, Clinical Development, Clinical Operations, Medical Affairs, CROs, and other internal stakeholders.
• Compliance & Quality: Conduct all activities in compliance with applicable laws, regulations, industry codes, and company policies.

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 Neuromuscular Diseases and/or Rare Diseases is mandatory.

Languages

Fluent English is required. Fluent Dutch and/or French is strongly preferred. Additional European languages are considered an advantage.

How to Apply

If you are passionate about advancing clinical research in neuromuscular diseases and want to make a meaningful impact on patients' lives, we encourage you to apply. Please submit your CV in English. Applications will be reviewed on an ongoing basis.

For questions or reasonable accommodations during the recruitment process, please contact: Laura Franco 📧 laura.franco@amplity.com