Join the LINK Medical Regulatory team in Oslo

LINK Medical Research
Regulatory Manager

LINK Medical is searching for a Regulatory Manager. Our company is growing, and the portfolio of regulatory customers requesting support in the product development phase as well as the life cycle management phase is increasing. LINK Medical is committed to the development of our employees and to create partnerships with our customers. By joining LINK Medical you will have the opportunity to work with a broad specter of Life Science customers and to develop into an expert in the regulatory field.

We are seeking highly motivated team players to join our team of regulatory experts. As a Regulatory Manager, you will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas. As a consultant in LINK Medical, you will deliver high-quality services in accordance with our customer expectations. You will have the opportunity to develop your competence according to our customer needs and participate in activities related to business development. Further, you will have the opportunity to grow your competency and your network through participation in exiting projects and tasks. This will set the right candidate up for continuous development and future career opportunities within the regulatory field, or within other areas where LINK Medical provides services.

Desired qualifications:

  • Natural science degree at college/university level
  • Experience within Regulatory Affairs is desirable
  • Generally good IT skills
  • Fluent in Norwegian and English (written and oral)

Personal characteristics:

  • Takes initiative
  • Service-minded with good cooperation and communication skills
  • Accurate
  • Flexible, open-minded and solution-oriented
  • Driven by continuous learning and development opportunities


  • Complete projects/services according to the agreement with the project manager, line manager, and customer
  • Ensuring customers’ positive perception of the collaboration with LINK Medical
  • Translations and update of Product Information documents including proof-reading, maintenance of texts intended for Felleskatalogen
  • Translation of educational material
  • Review, compilation, and submission of a regulatory dossier
  • Post-marketing regulatory maintenance activities
  • Regulatory support, e.g. consultation and advice on national legislation and specific requirements
  • Review of marketing material according to national pharma code
  • Contribute to the development of your area of expertise within LINK Medical
  • The position might be out-sourced to customers in the greater Oslo area

Contact information:

If you would like to know more or have any questions about the position, please contact Grethe Berven, Director, Regulatory & Safety in Norway, phone no. +47 920 25 155

All applications are treated confidentially.

Last day for application: 30.november 2019

Om arbeidsgiveren

LINK Medical is a full-service contract research organization (CRO) providing product development services for the pharmaceutical and medical device industries across Northern Europe. Our Scandinavian roots and culture provide a high-quality service delivery based on respect, work integrity and a strong focus on solutions. We are a pragmatic problem-solver, empowering our experienced specialists with modern technology that will change your expectations of a CRO partner. Our promise is to improve and accelerate your product development through transformative methods, active communication and optimal solutions

Gjerdrums vei 19, 0484 Oslo
Farmasi og legemiddel


Medicinal products, CRO, Regulatory Affairs, Marketing authorisation, Farmasøyt

Spørsmål om stillingen

Grethe Berven
Director Regulatory & Safety
920 25 155
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61 følger dette firmaet

Gjerdrums vei 19, 0484 Oslo

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FINN-kode 162495280
Sist endret 18. des. 2019 14:56

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