Principal Consultant - Regulatory Affairs

NNIT

Dublin, IEonsitePosted Jun 29, 2026
Posting intelligenceActively listedReposted 24×, possible evergreen/ghost posting

Skills

fhir

About the role

8 locations available

|

req1700

Share

Save Job

Posted on: 29/06/2026

Back to Search

Job available in these locations:

Denmark

Follonica GR, Italy

Dublin, Ireland

Saint Asaph, London, United Kingdom

Madrid, Spain

Kraków, Poland

Germany

Basel, Switzerland

Principal Consultant - Regulatory Affairs

Denmark, Germany, Italy, Switzerland, Spain, UK, Ireland, Poland

.nnit-hero__inner { background-image: url('https://mikkeltschentscher.dk/hosting/nnit/assets/images/hero.png'); }

Details

Type of contract: Permanent

Location(s): Denmark, Germany, Italy, Switzerland, Spain, UK, Ireland, Poland

Language(s): English

Mobility: Travel Required

Application Deadline: 31/08/2026

Principal Advisory Consultant - Regulatory Affairs:

NNIT is one of the world’s leading consultancies serving the life sciences industry globally. For more than twenty years, we have enabled our customers to achieve their business goals through digitalization within Quality Assurance, Regulatory Affairs, Clinical, Pharma Production and Laboratory processes.

To further strengthen our Regulatory Affairs team, we are looking for a Principal Advisory Consultant with significant Regulatory Affairs experience and strong expertise within FHIR and healthcare interoperability standards.

You will play a key role in shaping and growing our Regulatory Affairs advisory services with focus on structured data, interoperability, and digital regulatory transformation.

Your responsibilities:

You will join our Regulatory Affairs team as a Principal Advisory Consultant. You will contribute to forming the strategy for growing the Regulatory Affairs business unit with focus on FHIR and structured data, and you will be co responsible for executing this strategy through business development, thought leadership, and client delivery.

On average you will split your time:

60% delivering consultancy projects in advisor, project lead, architect, or engagement delivery lead roles with focus on FHIR enabled regulatory solutions

20% business development, presales, and thought leadership activities within Regulatory Affairs and interoperability

10% development of consultancy offerings, delivery methodologies, and training materials related to FHIR and digital regulatory transformation

5% development and delivery of RFP responses to secure new and expanded client engagements

5% coaching and mentoring consultants across all levels within the Regulatory Affairs team

In your client engagements, you will:

Advise on implementation and governance of FHIR standards in regulatory contexts

Support integration of FHIR with RIM systems, IDMP, and structured content management platforms

Translate global regulatory requirements into compliant, data driven and interoperable solutions

Act as trusted advisor to senior stakeholders in pharmaceutical, biotech, and medtech organizations

Drive alignment between business, regulatory, and IT functions

Your qualifications and experience:

Essential requirements:

Bachelor degree or equivalent in Pharmaceutical Compliance, Regulatory Affairs, Life Sciences, or related discipline

Significant experience in Regulatory Affairs within a pharmaceutical, biotech, or medtech company or as a consultant

Proven consulting experience within a recognized consultancy serving life sciences clients

Strong knowledge of FHIR and its application in healthcare data exchange and regulatory use cases

Experience with global regulatory frameworks including EMA and FDA

Demonstrated experience in sales and business development within a consulting environment

Strong stakeholder management skills and ability to engage clients, partners, and vendors

Excellent documentation, communication, and interpersonal skills in English

Preferred requirements:

Master degree in Pharmaceutical Compliance, Regulatory Affairs, or related field

Experience with RIM systems and IDMP

Knowledge of data governance and Master Data Management principles

Experience bringing new products to market in regulated environments

People management experience and track record of leading complex multi stakeholder projects

Project management experience with consistent on time and on budget delivery

Fluency in an additional European language such as German, Danish, Italian, Spanish, or French

Why join NNIT

A dynamic workplace with strong professional community and focus on collaboration

Opportunity to work with leading life sciences companies across Europe

Influence on strategic direction and growth of our Regulatory Affairs advisory services

Competitive salary, bonus, and benefits package

Clear personal development model supporting your long term career goals

Multicultural environment with an open and professional working culture

We are hiring into our European team in the following countries: UK and Europe – the role can be based in any European country where NNIT has an office location – Denmark, Germany, Ireland, Switzerland, Italy, Spain

Fluency in oral and written English is a must. A second language (Danish, German, Italian, Spanish or French) is desired but not essential.

Travel must be expected, but will be kept to necessary business trips (< 10%).

What’s next?

If you recognize yourself in this role, we’ll be looking forward to hearing from you. Please apply with a full resume and references that describe your abilities with regard of taking this leading role in NNIT’s Lab Consulting team.

and make your mark!

About NNIT

NNIT is a publicly listed company that specializes in IT solutions to life sciences internationally, and to the public and enterprise sectors in Denmark. We focus on high complexity industries and thrive in environments where regulatory demands and complexity are high. We advise on and build sustainable digital solutions that work for the patients, citizens, employees, end users or customers. NNIT consists of group company NNIT A/S and subsidiaries SCALES, Excellis Health Solutions and SL Controls. Together, these companies employ more than 1,800 people in Europe, Asia, and USA.

We celebrate diversity and are committed to creating an inclusive environment for all employees. All candidates are encouraged to apply for the given job regardless of their gender, age, religious beliefs, sexual orientation, national and social origin, political opinion, disability, race, skin colour, and ethnic origin.

In the interest of fostering a fair and unbiased recruitment process, we kindly request candidates to refrain from including their pictures in their applications.

Learn more about working at NNIT

and liberate your talent!

Share

Save Job

Questions about this role

Click "Apply with AI Applyd" above. We auto-fill the application from your resume and answer screening questions in seconds. No copy and paste, no juggling tabs.

Compensation for Teacher roles in Ireland varies widely by seniority, employer size, and remote vs onsite arrangement. Check the salary range on this listing when published, or browse our Teacher hub for Ireland medians across recent openings.

Most applications complete in under 90 seconds. You can track the status in your dashboard and watch the screenshot proof land the moment the application submits.

AI Applyd supports Greenhouse, Lever, Ashby, Workday, iCIMS, SmartRecruiters, Personio, Teamtailor and other major ATS platforms. If we can submit through the platform, we do.

Want AI Applyd to auto-apply to roles like this?

We tailor your resume per posting, fill the forms, and track replies for you.