Consultants Regulatory Affairs and/or Drug Development, NDA
Search4S Dustgoat AB / Biomedicinjobb / Upplands Väsby
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hela Sverige Do you know the regulatory requirements for a part of the drug development process or life cycle management? Are you interested in expanding your knowledge into new therapy areas and different kinds of projects? If you also would like to work closely to highly experienced colleagues as in-house consultant, NDA's looking for more Consultants and Senior Consultants!
NDA is a global regulatory affairs consultancy with headquarters in Sweden. We are providing global, local, large and small pharmaceutical companies with operational and strategical advice within drug development and life cycle management. Over the last 5 years we have been involved in ca 40% of all applications for market approval in EU.
As Consultant at NDA you work next door to you colleagues, with varying projects corresponding to your expertise. Depending on your background and expertise, you'll have different assignments. Read more about this job and life a consultant at NDA here:
https://search4s.teamtailor.com/pages/consultants-ndaLocation: Upplands Väsby with possibilities to work part-time from a distance.
Terms: This is a full-time open-ended position with NDA as employer.
Start: As soon as possible or upon agreement.
Qualifications
We are looking for regulatory experts within drug development and/or life cycle management, with a few years or decades of experience. As a consultant, you'll work with different projects, therapy areas and clients. You need to enjoy expanding your knowledge, adapting to a variety of situations and making efforts to create effective team-work. As a senior Consultant you should also be comfortable in leading projects and international collaborations.
• Several years of experience from the pharmaceutical industry and/or regulatory agencies.
• Experience from coordination or project management of e.g. clinical trial applications, variation applications and marketing authorisation applications for EU and/or USA, orphan drug designation applications (ODD), Paediatric Investigation Plans (PIP), Scientific Advice procedures etc.
• Academic degree within life science.
• Excellent spoken and written English.
• Spoken and written Swedish is meriting
Application and information:
In this recruitment NDA is working with Search4S. For more information contact Recruitment Consultant Anna Rennermalm, +46 707 94 20 05 or
anna@search4s.se.
Last application date: March 23 2021
Interviews and selection of candidates will be continuous. Note that the application should be sent through this link and not by email:
About NDA Regulatory Services AB
NDA Group is a world leading regulatory, drug development and medical device consultancy. We have a dedicated team of over 150 consultants supported by an expert network and a specialist Advisory Board many of whom are ex- European and US Agency staff.
NDA Group supported close to 40% of the new medicinal products that were approved in the EU over the last five years.
http://www.ndareg.com/) www.ndareg.com (
http://www.ndareg.com)Varaktighet, arbetstid
Heltid Anställningstid enligt överenskommelse
Publiceringsdatum2021-03-01ErsättningLön enligt överenskommelse
Så ansöker duSista dag att ansöka är 2021-03-23
Klicka på denna länk för att göra din ansökanFöretagSearch4S Dustgoat AB
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Search4S Dustgoat AB (org.nr 559065-9297),
http://www.Search4s.se Arbetsplats Search4s Dustgoat AB
Jobbnummer 5602736
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