I contribute to clinical research with expertise and empathy. And I do it
Regulatory Affairs Consultant – Germany & Austria (Munich on-site)
Primary Location: Germany, Remote Job ID R0000045589 Category Regulatory / Consulting Date Posted 09/03/2026Overview
As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there.
We value collaboration, innovation, and continuous learning. As a member of our team, you will partner with a diverse group of clients, and be exposed to various product types and therapeutic areas. You will also develop your skills through challenging assignments and mentorship from experienced regulatory professionals. Plus, you will enjoy the flexibility of working remotely while still being part of a supportive and dynamic team.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Problem-solver
- Relationship-builder
- Results-driven
- Strategic
About This Role
About the Role
We are seeking an experiencedRegulatory Affairs Professional to provide comprehensive regulatory support for Germany and Austria. This is a strategic role that combines deep regulatory expertise with business acumen, supporting our client's mRNA therapeutics and vaccines across Germany and Austria.
This role requires at least one day per week on-site presence (the office is in Munich).
Key Responsibilities
Regulatory Strategy & Guidance: Deliver forward-looking, pragmatic, and creative strategic regulatory guidance to affiliate and brand teams, anticipating regulatory challenges and providing agile solutions
Regulatory Compliance & Operations: Support local business objectives through coordination of cross-functional reviews, translations of product information, artwork management, and market implementation activities
Stakeholder Management: Review promotional materials and medical communications; provide regulatory training and updates to local affiliate teams; represent the Regulatory Affairs team in internal, affiliate, and cross-functional meetings
Market Access Support: Coordinate regulatory activities related to pricing, reimbursement, and tender processes
Authority Relations: Manage and coordinate interactions with German and Austrian regulatory authorities concerning client's pipeline and licensed products
Project Leadership: Independently manage multiple complex regulatory projects in a fast-paced environment while maintaining precision, compliance, and strategic judgment
Innovation & Efficiency: Explore opportunities to leverage Generative AI and emerging digital capabilities to enhance regulatory intelligence, content workflows, and operational efficiency
Leadership Support: Deputise for the Director, Regulatory Affairs Strategy – Germany and Austria as needed
Required Skills and Qualifications:
University Degree in a Scientific or Technical Discipline (Advanced Degree preferred)
Extensive years of experiencein regulatory affairs and regulatory strategy
Deep knowledge of German, Austrian, and European pharmaceutical regulations, including: innovative medicines and vaccines, drug development and marketing authorisation procedures, line extensions and lifecycle management
Strong working knowledge of regulatory systems and tools (artwork management systems, text-verification tools, electronic document/data management systems)
Strategic thinking and sound regulatory judgment
Critical thinking and problem-solving expertise
Client-focused approach with consulting acumen
Fluent in German and English(written and verbal)
#LI-REMOTE
Employee Insights
Why Consultants work at Parexel
