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Open nowPosted 53 days ago

Local PV Support Person and Medical Information Specialist - Iceland (Freelance)

Workable (global search)108,016 open roles

Where
Iceland
Work mode
Remote
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Your applicationOpen nowLocal PV Support Person and Medical Information Specialist - Iceland (Freelance)Workable (global search) · Iceland

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The clock on this job

Early applications get read.

7.9% of postings close within 7 days. Measured by our own scanner across the market. Workable (global search) postings stay open a median of 7 days.

Share of postings closed within
  1. 1.6%1 day
  2. 3.6%3 days
  3. 7.9%7 days
  4. 14.9%14 days
  5. 34.0%30 days
This job: posted 53 days ago

Workable (global search) median: 7 days open

The posting

Freelance opportunity in Iceland! Join our global team as a Local Pharmacovigilance Support Person and Medical Information Specialist in Iceland.

Local Pharmacovigilance Support Person and Medical Information Specialist is responsible for managing daily operations, ensuring compliance, exchanging safety information and serving as a contact for timely safety processing.

Position is remote for 0.1 FTE position in Iceland, working in close collaboration with Nordic local safety officers and medical information specialists.

You have energy and motivation to work in a team and to gain more experience?

Submit your CV in the English language for consideration.

Responsibilities:

  • Perform local PV operations and ensure compliance with safety regulations and procedures
  • Manage ICSRs and FUs
  • Review local literature
  • Review local legislation
  • Perform PV trainings to MAH employees
  • Handle Medical Information Requests
  • Support Biomapas Clients with other PV related tasks

Requirements

  • Degree in Medicine, Biomedicine, Pharmacy, or Nurse
  • Fluent in written and spoken English and native Icelandic
  • Preferably at least 2 years experience in pharmacovigilance
  • In-depth, demonstrated experience in most areas pertaining to pharmacovigilance and pharmacovigilance legislation
  • Excellent knowledge of local and international regulations (ICH, EU GVP Modules)
  • Analytical skills to understand, analyze, interpret, and present scientific data
  • Ability to interpret and apply global and local drug safety regulations
  • High motivation to develop and learn within the team
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