IDMP and Regulatory Affairs Consultant
Denne stilling er desværre ikke længere ledig.
Se alle ledige stillinger
Storkøbenhavn
In NNIT RA, we guide our customers through the digital business transformation; with knowledge, experience, dedication, and trust, we help our customers impact patients’ lives.
NNIT Regulatory Affairs is a leading global RA advisory and consultancy organization committed to digitally transform Regulatory Affairs into an influential, strategic and data driven business unit.
We are looking for Senior/Principal Consultant with deep IDMP and Regulatory Affairs expertise who wishes to make a mark on some of the most exciting IDMP projects in the life science industry.
Are you driven by leveraging your IDMP expertise with digital acumen, having responsibility and ownership of projects, and do you want to change the life science industry?
Then you are a perfect match for the role as our new RA colleague.
Your responsibilities as a Regulatory Affairs Consultant
You will join an exciting, international department with highly skilled colleagues that have a deep understanding of the industry and the ability to bridge this knowledge with digital technologies and deliver the highest quality implementations.
Working closely with clients, you will use your experience to assist companies in a vast array of projects, spanning from IDMP process optimizations, IDMP data governance implementations and IDMP data quality assessments.
You will be expected to direct the clients on regulatory requirements and technologies to meet the IDMP data scope. You’re likely to have knowledge about RIMS systems, in particular Veeva Vault RIM. Part of the job is also business development activities related to IDMP that will support our continued growth within the area of Regulatory Affairs.
The job will include close collaboration with a multitude of stakeholders within NNIT where your business domain knowledge will strengthen our companies' strategic aspirations in Regulatory Affairs.
If you are interested in giving presentations at conferences and working groups on IDMP, this would be very welcome and will be part of your development plan.
Your career will include continuous training and competence development to support our department and your personal ambitions.
You will be part of NNIT’s Regulatory Affairs Consulting
NNIT Regulatory Affairs is at the forefront of supporting global pharmaceutical and medical device clients on the latest digital trends within Regulatory Affairs and Safety.
Our commitment to the life science industry is reinforced in our devotion to the advisory and consultancy unit. This makes us stand out, is key to our costumer success and emphasize our leadership position in RA consulting.
The specialized RA consultancy team is dedicated to leverage RA knowledge with the newest technology, to ensure highest quality across implementation projects in close collaboration with the RA Advisory team.
We are an ambitious department with highly skilled colleagues with deep understanding of the industry. We are a diverse mix of nationalities with different educational backgrounds and an even mix of gender.
Your qualifications and experiences
You may hold an MSc degree in life sciences or IT with solid experience from Regulatory Affairs or consultancy in RA with focus on IDMP. You have an interest in and an understanding of IT, and you manage to bridge your professional experience with IT and build solid implementations with the costumer in focus.
Experience with agile delivery such as SAFe is an advantage.
It is an advantage if you have experience with Regulatory business processes and how digitalization can support business process efficiency. You know that a winning personality will help you build trust and enable great customer engagement, and you might have gained this experience from a past job within the consulting area.
We appreciate openness, honesty, and a winning attitude.
We expect that you are quickly integrating with customers and internal teams and that the customer satisfaction will be key to your personal success.
NNIT has offices in Copenhagen, Frankfurt, and Basel, and you might live in the proximity of these pharma hubs.
Fluency in oral and written English is a must. German, French and/or Danish is beneficial.
Depending on your location and specific project responsibilities, travel must be expected.
About NNIT Regulatory Affairs
The NNIT Group provides a wide range of IT and consulting services to the global life science industry and has been a trusted partner to life science companies for +25 years.
We are a leading global RA advisory and consultancy organization committed to digitally transform Regulatory Affairs into an influential strategic and data driven business unit.
We leverage thought leadership knowledge and the newest technology, with implementation excellence and successive maintenance service.
NNIT Regulatory Affairs is a leading global RA advisory and consultancy organization committed to digitally transform Regulatory Affairs into an influential, strategic and data driven business unit.
We are looking for Senior/Principal Consultant with deep IDMP and Regulatory Affairs expertise who wishes to make a mark on some of the most exciting IDMP projects in the life science industry.
Are you driven by leveraging your IDMP expertise with digital acumen, having responsibility and ownership of projects, and do you want to change the life science industry?
Then you are a perfect match for the role as our new RA colleague.
Your responsibilities as a Regulatory Affairs Consultant
You will join an exciting, international department with highly skilled colleagues that have a deep understanding of the industry and the ability to bridge this knowledge with digital technologies and deliver the highest quality implementations.
Working closely with clients, you will use your experience to assist companies in a vast array of projects, spanning from IDMP process optimizations, IDMP data governance implementations and IDMP data quality assessments.
You will be expected to direct the clients on regulatory requirements and technologies to meet the IDMP data scope. You’re likely to have knowledge about RIMS systems, in particular Veeva Vault RIM. Part of the job is also business development activities related to IDMP that will support our continued growth within the area of Regulatory Affairs.
The job will include close collaboration with a multitude of stakeholders within NNIT where your business domain knowledge will strengthen our companies' strategic aspirations in Regulatory Affairs.
If you are interested in giving presentations at conferences and working groups on IDMP, this would be very welcome and will be part of your development plan.
Your career will include continuous training and competence development to support our department and your personal ambitions.
You will be part of NNIT’s Regulatory Affairs Consulting
NNIT Regulatory Affairs is at the forefront of supporting global pharmaceutical and medical device clients on the latest digital trends within Regulatory Affairs and Safety.
Our commitment to the life science industry is reinforced in our devotion to the advisory and consultancy unit. This makes us stand out, is key to our costumer success and emphasize our leadership position in RA consulting.
The specialized RA consultancy team is dedicated to leverage RA knowledge with the newest technology, to ensure highest quality across implementation projects in close collaboration with the RA Advisory team.
We are an ambitious department with highly skilled colleagues with deep understanding of the industry. We are a diverse mix of nationalities with different educational backgrounds and an even mix of gender.
Your qualifications and experiences
You may hold an MSc degree in life sciences or IT with solid experience from Regulatory Affairs or consultancy in RA with focus on IDMP. You have an interest in and an understanding of IT, and you manage to bridge your professional experience with IT and build solid implementations with the costumer in focus.
Experience with agile delivery such as SAFe is an advantage.
It is an advantage if you have experience with Regulatory business processes and how digitalization can support business process efficiency. You know that a winning personality will help you build trust and enable great customer engagement, and you might have gained this experience from a past job within the consulting area.
We appreciate openness, honesty, and a winning attitude.
We expect that you are quickly integrating with customers and internal teams and that the customer satisfaction will be key to your personal success.
NNIT has offices in Copenhagen, Frankfurt, and Basel, and you might live in the proximity of these pharma hubs.
Fluency in oral and written English is a must. German, French and/or Danish is beneficial.
Depending on your location and specific project responsibilities, travel must be expected.
About NNIT Regulatory Affairs
The NNIT Group provides a wide range of IT and consulting services to the global life science industry and has been a trusted partner to life science companies for +25 years.
We are a leading global RA advisory and consultancy organization committed to digitally transform Regulatory Affairs into an influential strategic and data driven business unit.
We leverage thought leadership knowledge and the newest technology, with implementation excellence and successive maintenance service.
- Rated as Leading RA Consultancy by GENS & ASSOCIATES
- Rated as most Responsible and Trustworthy IT consultancy house with Highest Quality and Best Implementation Skills by MyResearch in DK
- First Veeva Premiere Services Partner
- 100+ RA dedicated consultants in DK, CH, DE, CN, US
- 30+ Current RA clients, incl. several tier 1 pharma clients
- 3000+ Employees in NNIT globally
Information og data
Denne ledige stilling har jobtypen "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Storkøbenhavn
Jobbet er oprettet på vores service den 12.7.2021, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Apoteker
- Storkøbenhavn
- Torsdag den 30. september 2021
Lignende jobs
-
Director, Global Regulatory Affairs - CMC
At [xxxxx], we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and th..Få mere info- Apoteker
- København
-
Executive Management Assistant at Xellia Pharmaceu...
Are you ready to make a difference and play a crucial role in an organization dedicated to saving lives? Are you the person who cares about making your executives everyday life work, and have you d..Få mere info- Apoteker
- København
-
Safety Operations Outsourcing Specialist
Do you have solid knowledge of drug safety/pharmacovigilance and clinical drug development, combined with project management experience? Do you have a strategic mindset and strong communication ski..Få mere info- Apoteker
- Søborg
-
Planner søges til [xxxxx] til Pharma
Har du en analytisk tilgang til opgaverne og brænder for at tage strategiske beslutninger? Har du lyst til at arbejde sammen med dedikerede og dygtige kollegaer, hvor ordentlighed er indbegrebet af..Få mere info- Apoteker
- Hvidovre
Statistik over udbudte jobs som apotekere i Storkøbenhavn
Herunder ser du udviklingen i udbudte apoteker i Storkøbenhavn over tid. Bemærk at jobs der ikke har en bestemt geografi ikke er medtaget i tabellen. I den første kolonne ser du datoen. I den næste kolonne ser du det samlede antal apotekere i Storkøbenhavn.
Se flere statistikker her:
Statistik over udbudte apotekere i Storkøbenhavn over tid
| Dato | Alle jobs som apotekere |
|---|---|
| 27. november 2024 | 30 |
| 26. november 2024 | 28 |
| 25. november 2024 | 28 |
| 24. november 2024 | 30 |
| 23. november 2024 | 30 |
| 22. november 2024 | 30 |
| 21. november 2024 | 30 |
| 20. november 2024 | 30 |
| 19. november 2024 | 33 |
| 18. november 2024 | 38 |
| 17. november 2024 | 38 |
| 16. november 2024 | 36 |
| 15. november 2024 | 38 |
| 14. november 2024 | 38 |
| 13. november 2024 | 36 |
| 12. november 2024 | 33 |
| 11. november 2024 | 33 |
| 10. november 2024 | 30 |
| 9. november 2024 | 33 |
| 8. november 2024 | 31 |
| 7. november 2024 | 31 |
| 6. november 2024 | 31 |
| 5. november 2024 | 33 |
| 4. november 2024 | 31 |
| 3. november 2024 | 32 |
| 2. november 2024 | 32 |
| 1. november 2024 | 33 |
| 31. oktober 2024 | 30 |
| 30. oktober 2024 | 28 |
| 29. oktober 2024 | 28 |
| 28. oktober 2024 | 28 |