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 proceduresManage ICSRs and FUsReview local literatureReview local legislationPerform PV trainings to MAH employeesHandle Medical Information RequestsSupport Biomapas Clients with other PV related tasksRequirementsDegree in Medicine, Biomedicine, Pharmacy, or NurseFluent in written and spoken English and native IcelandicPreferably at least 2 years experience in pharmacovigilanceIn-depth, demonstrated experience in most areas pertaining to pharmacovigilance and pharmacovigilance legislationExcellent knowledge of local and international regulations (ICH, EU GVP Modules)Analytical skills to understand, analyze, interpret, and present scientific dataAbility to interpret and apply global and local drug safety regulationsHigh motivation to develop and learn within the team
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
Biomapas is a functional and full outsourcing solution provider to the global life science industry.
As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle.
Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success.
Biomapas is a functional and full outsourcing solution provider to the global life science industry.
As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle.
Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success.
