Local PV Support Person and Medical Information Specialist - Iceland (Freelance)
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Before you apply
LocationIceland
Work moderemote
Typepart-time
SeniorityMid
Experience2+ yrs
DepartmentPV/RA/MI Operations
Company size51–200 people
PostedAug 12, 2026 · 2mo ago
Verified live4h ago
At a glanceSummarised by Seekless from the posting.
Degree in Medicine, Biomedicine, Pharmacy, or Nurse
Fluent in written and spoken English
Native Icelandic
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
At least 2 years experience in pharmacovigilance
About the role
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?
Hiring process
Submit your CV in the English language for consideration.
Responsibilities:
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Perform local PV operations and ensure compliance with safety regulations and procedures
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Manage ICSRs and FUs
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Review local literature
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Review local legislation
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Perform PV trainings to MAH employees
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Handle Medical Information Requests
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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