Asphalion’s Regulatory and Strategic Consulting team offers comprehensive support throughout the drug development process, from initial stages to market launch.

Our team has academic research experience and a broad scientific background in non-clinical, clinical and CMC writing for different types of products, including innovative, biological, biotechnological and advanced therapies medicinal products.

Asphalion’s expertise allows us to offer the best regulatory strategy for each project!

Joining us you will participate in different projects with all sort of regulatory related documentation required during the clinical development and registration.

In addition to this, strategic inputs can be provided from the very beginning for segmentation/niche indication, conditional approval/fast track, orphan drug designations, preclinical and clinical development plans with minimal time-to-market, among others.

Why working at Asphalion?





?️Permanent contract.

? Adaptable working schedule - Friday until 15.30h.

? Homeoffice & Hybrid or Remote Model

⚙️ Wide variety of projects, new challenges and experiences.

↗️ Training and personal development program.

?English lessons.

? A professional, inclusive and high-performance work environment to develop your skills and grow your career. A great company culture built around Passion, Flexibility, Commitment, Quality & Companionship.

?A highly & dynamic working environment with employees from more than 15 nationalities.

??Our people and their well-being are our priority: Physical, psychological and emotional well-being programme.

? Internal activities & RSC Activitie

✅ Equal Opportunity Employer

📌 BIOSPAIN 2026 (Barcelona)
🏢 Asphalion
📍 Barcelona