
Junior Legal Associate
Ardena Careers
Ghent, Flemish Region, Belgium
Legal / Public / Security
As a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO), Ardena partners with pharmaceutical and biotech companies to turn scientific ideas into real treatments. From early development to manufacturing and regulatory support, we help bring new medicines to market faster and with the highest quality standards.
With more than 750 colleagues across Europe and the United States, Ardena offers expertise in drug substance and drug product development, manufacturing, bioanalytical services, clinical logistics, fill & finish, and CMC regulatory support.
But what truly makes Ardena special is our people. We are a science-driven and people-focused company where collaboration, innovation, and curiosity are encouraged.
We offer an international environment where you can learn, take initiative, and grow your career across teams, functions, and locations. Our way of working is guided by our CARE values: Communicative, Accountable, Reliable, and Excellent. These values shape how we collaborate, solve challenges, and support each other every day.
At Ardena, you’re not just building your career — you’re helping build the future of medicine.
For our Corporate Legal department, based in Wondelgem (Gent, Belgium), we are looking for a motivated and detail-oriented
JUNIOR LEGAL ASSOCIATE
YOUR KEY ROLE
This is an entry-level position designed for recent law graduates who are eager to start their legal careers. No prior professional experience is required, just an eagerness to learn, good attention to detail, and a solid academic foundation.
Your Key Responsibilities
- Contract drafting: You assist in drafting, reviewing, and negotiating a range of agreements, such as clinical trial agreements, confidentiality agreements, licensing deals, and vendor contracts.
- Compliance: You support compliance initiatives related to pharmaceutical regulations, GDPR, anti-bribery laws, and industry codes of conduct.
- Legal research: You conduct legal research on applicable laws, regulations, and emerging industry trends, and translate findings into practical business guidance.
- Automation and AI: You leverage AI-driven legal tools and automation technologies to enhance efficiency in contract review, legal research, and document management; you support the development of automated templates and self-service tools; you identify opportunities to streamline legal workflows; and you contribute to internal guidance on the responsible, compliant use of AI, including monitoring relevant legal and regulatory developments.
- Archiving: You maintain organized and up-to-date legal documentation, including contract repositories and knowledge management systems.
- You report to the Corporate Legal Counsel
- Master’s degree in law
- Fluent in English
- Excellent written and verbal communication skills
- Analytical thinking and attention to detail
- Excellent organizational skills and ability to manage multiple tasks and meet deadlines
- Self-starter who is curious, loves AI and technology, and thrives in a dynamic environment
- You are stress-resistant, solution-oriented, and driven by a 'make-it-work' mindset
- You show flexibility and you are open-minded and change oriented (always looking for ways to improve)
- You are a team player
- Proficiency in Microsoft Office (Word, Excel, PowerPoint)
- A true learning environment where you will have the ability to grow your skills
- A rapidly international developing and growing company with an interesting services, product and customer portfolio
- A dynamic working environment with nice colleagues
- Open straightforward but also caring culture
- We love creative thinking and pro-activeness
- We are true to our values
- An attractive remuneration package including extra-legal benefits such as: group insurance, hospitalization insurance, meal vouchers, eco vouchers and a group bonus system
About the company
Company website•Pharmaceutical Manufacturing
Find your career path with Ardena
At Ardena, we’re more than a global Contract Development and Manufacturing Organization (CDMO) - we’re a team of innovators, problem-solvers, and experts dedicated to advancing drug development. With over 750 professionals across Belgium, the Netherlands, Spain and the US, we help biopharma companies navigate complex challenges and bring new therapies to patients.
Whether you’re a scientist, engineer, project manager, or business professional, Ardena offers dynamic career opportunities, global collaboration, and a people-first CARE culture where you can grow, innovate, and make a real impact. Join us and together, we’ll transform your potential and the future of medicine!
When you join Ardena, you gain:
✔ Diverse Projects – Work on breakthrough therapies across a range of customers and drug types.
✔ Global Collaboration – Connect with colleagues across Belgium, the Netherlands, Sweden, Spain, and the US.
✔ Comprehensive Training – Benefit from our Ardena Academy, onboarding programs, and ongoing career development.
✔ Career Growth – Advance your skills with mentorship, learning opportunities, and leadership pathways.
✔ A People-First Culture – Enjoy a supportive, international work environment that values collaboration and innovation.
At Ardena, your career growth knows no limits. Whether you’re starting with an internship, joining as an experienced professional, or looking to expand your expertise, we provide the tools, support, and opportunities to help you succeed.
🔍 Ready to start your career path with Ardena? Explore our careers: https://careers.ardena.com/