Clinical Affairs Specialist (Pharmaceuticals & Medical Devices) (F/M/X)

We are looking for a Regulatory Affairs / Clinical Affairs Specialist with strong experience in pharmaceuticals and medical devices.

• Manage regulatory projects in pharmaceuticals and medical devices
• Advise clients on regulatory compliance, product registration, and market access
• Prepare and submit regulatory dossiers to competent authorities
• Monitor regulatory changes and anticipate legislative developments
• Support clients during audits and inspections
• Optimize internal processes related to compliance and quality
• Deliver training and guidance to client teams on regulatory requirements
• Collaborate with multidisciplinary teams to ensure project success
• Experience in regulatory affairs for pharmaceuticals and medical devices (5-15 years)
• Proficiency with industry-specific tools and software
• Academic background in Life Sciences, Pharmacy, Engineering, or related field
• English fluent. French is a plus.
• You demonstrate strong analytical and problem-solving skills

What You’ll Get From Us:

• Be part of a very international and diverse team
• Part-time work from home and work from office
• Ability to work from different offices in different cities and countries
• Long-term career planning as part of periodic performance reviews
• Professional development plans are tailored to each member of the team
• Ability to branch out into other areas such as market access, pricing, statistics, RWE, etc.
• Strong opportunity to bring in your ideas and leave your mark on the organization
• Competitive salary and compensation

Amaris Consulting is committed to diversity and inclusion. We welcome applications from all qualified individuals, regardless of gender, sexual orientation, race, ethnic origin, beliefs, age, marital status, disability, or any other characteristic.