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Local Safety Officer/Medical Information Specialist (freelance role)

extra parental leave - fully flexible
Remote: 
Full Remote
Contract: 
Experience: 
Junior (1-2 years)
Work from: 

Offer summary

Qualifications:

Degree in Medicine, Biomedicine, Pharmacy or Nursing, Fluent in English and at least one Nordic language, 1-2 years experience in pharmacovigilance, Knowledge of local and international regulations.

Key responsabilities:

  • Manage daily operations and ensure compliance
  • Exchange safety information with authorities and clients
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Biomapas SME http://www.biomapas.com
201 - 500 Employees
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Job description

Freelance opportunity in Nordics! Join our global team as a Local Safety Officer and Medical Information Specialist in Nordics (Sweden, Norway or Denmark).

Local Safety Officer 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 part-time and remote for the Nordic countries (Sweden, Norway or Denmark), working in close collaboration with Finland and Iceland local pharmacovigilance support personnel.

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 operations and ensure compliance with safety regulations and procedures

• Manage and share safety information with relevant authorities and clients

• Serve as the main contact for safety matters with authorities and clients

• Ensure timely handling of safety information for products

• Review local literature

• Medical Information Requests handling

Requirements

• Degree in Medicine, Biomedicine, Pharmacist or Nurse

• Fluent written and spoken English and at least one of the following languages: Swedish, Norwegian or Danish

• Preferably at least 1-2 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

Required profile

Experience

Level of experience: Junior (1-2 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Teamwork
  • Self-Motivation
  • Communication

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