Senior ConsultantUK, Denmark, Italy, Poland, Czech, Ireland, Switzerland
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DetailsType of contract: PermanentLocation(s):UK, Denmark, Italy, Poland, Czech, Ireland, SwitzerlandLanguage(s):EnglishMobility: Some TravelApplication Deadline:10/30/2026Senior Consultant - Regulatory AffairsNNIT is one of the world's leading consultancies for the
past twenty years serving the Life Science industry around the world. We
strive to enable 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 Senior Consultant with a diverse skill set across
Regulatory Affairs in the life sciences industry including
some IDMP regulatory affairs exposure.
Your responsibilities:
You
will join our Regulatory Affairs team as a Senior Consultant. You
will contribute to forming a variety of tasks and functional
responsibilities within the Regulatory Affairs business unit such as taking ownership
of client engagements and specific projects, contribute to business development
and sales activities and contribute to and deliver Requests for Proposal
(RFP's) as required.
On average you will split your time:75% delivering in consultancy
projects in advisor, project lead or architect roles, and
acting as engagement delivery lead. 10% in
business development, presales and though leadership activities 10% in the development and
delivery of RFP's to ensure NNIT successfully engages new and additional
projects5%
in coaching and mentoring of more junior consultants
in the Regulatory Affairs team Your qualifications and experience: Essential requirements: A Bachelor's Degree (or similar) in a field related to Pharmaceutical Compliance or Regulation. Other relevant academic qualifications can be considered if you also have highly significant consulting and/or industry based experience inRegulatory Affairs within Life Sciences. Significant experience in Regulatory Affairs within a Pharmaceutical company or as a consultant.
Proven consulting based experience is an essential requirement for the role, ideally within a large recognised consultancy with a life sciences division or specialism. A proven level of experience in the area of IDMP including some of the following: Experience in IDMP data transformationData enrichment for PMS, RIMS and XEVMPDExperience with RIM systems related to IDMPFully aware and cognizant of current EMA updates on IDMPExperience presenting IDMP topics to larger audiencesProficiency in PMS and Postman APIExperience in managing interactions with clients, partners and vendors and an interest in driving and expanding NNIT client relations as part of business development, pre-sales and project delivery activities.
First class documentation, communication, and interpersonal skills, with an ability to liaise effectively and professionally with individuals at all levels.
Preferred requirements: A
Masters level qualification in a relevant area of study such as
Pharmaceutical Compliance or Regulation.
Regulatory
experience within the Pharmaceutical industry.
Consulting
experience within a recognised consulting firm.
Experience
working within Regulatory Affairs for a pharmaceutical company.
Experience
with Power BI application.
Phyton
coding and scripting experience.
Why should you join NNIT & What we offer to
you? A
dynamic workplace with good working conditions, social activities,
team events and work life balance.
Opportunity
to work in a multicultural company with a friendly and dynamic work
environment. Competitive
salary, additional bonus and benefit package (contribution
to your home internet, fitness funding, and others).An Informal
and friendly working culture between NNIT colleagues.
Opportunity
to work with the most significant life sciences clients. Diversity
of projects, and the possibility of shaping your own career path.
Personal
development model which defines your long-term career goals.
We are hiring into our European team in the following
countries: UK, Denmark, Italy, Poland, Czech, Ireland, SwitzerlandFluency in oral and written English is a must. A
second language (German, Danish, Italian or French) is
desired but not essential. Travel
must be expected, but will be kept to necessary business trips (<20%). 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 Regulatory Affairs team. Apply now and make your mark! About NNITNNIT 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 1,600 people in Europe, Asia, and USA.We celebrate diversity and are dedicated to fostering an inclusive environment for all employees. We actively work to eliminate bias and ensure an inclusive workplace where everyone has the right to be seen and heard as they are. We invite interested candidates to apply, no matter their background.
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 NNITApply now and liberate your talent!
Graduate Consultant / Consultant / Senior in London employer: NNIT
At NNIT, we pride ourselves on being an excellent employer, offering a dynamic workplace that fosters professional growth and collaboration within the life sciences sector. Our commitment to employee development is reflected in our mentorship programmes and opportunities to work with leading clients, all while enjoying a competitive salary and comprehensive benefits package. Join us in the UK to make a meaningful impact in Regulatory Affairs and advance your career in a supportive environment.
