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NorwayContractual TemporaryPolicy Administration Professionals

Regulatory Affairs Consultant

Apsida Life Science | Norway | Salary not specified

Source: JobsPipe

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Role snapshot

Work model
Remote
Language
Not specified
Experience
Not specified
Posted
Posted 1 day ago
Application deadline
2026-10-14

What you'll do

Job Title: Regulatory Affairs Consultant – Promotional Review (Norway) Location: Remote / Project-Based Contract duration: ASAP – December 31, 2026 (with potential extension into 2027) Hours: 30/month Start: ASAP Company Overview: Apsida Life Science is partnering with a leading global clinical research and biopharmaceutical services organization that supports pharmaceutical, biotechnology, and medical device companies across the full product development lifecycle. The organization provides expertise across clinical development, regulatory affairs, pharmacovigilance, medical communications, and market access, working with clients worldwide to advance innovative healthcare products and therapies. Key Responsibilities

  • Promotional Material Review: Perform expert regulatory review of digital and print promotional materials (including websites, digital assets, and publications) targeted for the Norwegian market.
  • Compliance Assurance: Ensure all messaging, product claims, and visual representations adhere to Norwegian Medicines Agency (NoMA / Direktoratet for medisinske produkter) regulations, local codes of practice, and advertising guidelines.Advisory
  • Guidance: Provide actionable regulatory feedback, risk assessments, and required copy amendments to ensure marketing assets meet local compliance standards prior to external publication.

Requirements:

  • Strong background in Regulatory Affairs within the biopharmaceutical or healthcare industry.
  • Demonstrated expertise in Norwegian local regulatory requirements governing the advertising and promotion of medicinal products/health products.
  • Proven track record in reviewing digital assets (websites, online banners) and print publications for market compliance.
  • High attention to detail with fluency in English (knowledge of Norwegian regulatory language standards is required).

Project Details:

  • Workload: Project-based, ad hoc engagement capped at a maximum of 30 hours total through year-end.
  • Timeline: Immediate start through December 31, 2026, with the possibility of extension into 2027 based on project needs.

If you are interested in learning more, please reach out to Tumi Sotia at Apsida Life Science: tumi.sotia@apsida.com +44 744 134 2145 Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost-effective, high-quality, and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.

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