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Skills: Pharmacovigilance, Literature Screening, Compliance, Safety Information, Quality Management
Join our global team as a Pharmacovigilance Specialist (Japanese Speaking) (Remote/home based). You will be mainly responsible for conducting global and local literature screening and assuring compliance with local and r…
Skills: Literature Screening, Pharmacovigilance, Japanese Fluency, English Fluency, MS Office
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Skills: Pharmacovigilance, Team Management, Regulatory Compliance, Project Management, Medical Writing
Join our Pharmacovigilance team as Associate Director International PV. Associate Director International PV is responsible for the leadership and oversight of the international PV office, ensuring compliance with interna…
Skills: Pharmacovigilance, Team Management, Regulatory Compliance, Project Management, Medical Writing
Join our Pharmacovigilance team as Associate Director International PV. Associate Director International PV is responsible for the leadership and oversight of the international PV office, ensuring compliance with interna…
Skills: Pharmacovigilance, Team Management, Regulatory Compliance, Project Management, Medical Writing
Join our Pharmacovigilance team as Associate Director International PV. Associate Director International PV is responsible for the leadership and oversight of the international PV office, ensuring compliance with interna…
Skills: Pharmacovigilance, Team Management, Regulatory Compliance, Project Management, Medical Writing
Join our Pharmacovigilance team as Associate Director International PV. Associate Director International PV is responsible for the leadership and oversight of the international PV office, ensuring compliance with interna…
Skills: Pharmacovigilance, Team Management, Regulatory Compliance, Project Management, Medical Writing
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Join our global team as Clinical Operations Lead. Clinical Operations Lead is responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assig…
Join our global team as Clinical Operations Lead. Clinical Operations Lead is responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assig…
Join our global team as Clinical Operations Lead. Clinical Operations Lead is responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assig…
Join our global team as Clinical Operations Lead. Clinical Operations Lead is responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assig…
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Full-time
professional certificate
Bonus Based On Annual Performance, Professional Growth And Career Opportunities, International Team And Environment, Personal Accident And Business Trip Insurance, Additional Health Insurance, Remote/Home Based
Posted 35d ago
~40 hrs/week
Remote in Germany
Responsibilities
The Pharmacovigilance Specialist will ensure weekly monitoring of local and global literature reviews and communicate with health authorities. They will also collect, process, and communicate safety information and maintain quality standards for local pharmacovigilance activities.
Requirements
Candidates must have a Pharmacist or Medical Doctor degree and at least 2 years of experience in literature screening for pharmacovigilance. Fluency in English and Japanese, along with strong organizational and time management skills, is required.
Full job description
Join our global team as a Pharmacovigilance Specialist (Japanese Speaking) (Remote/home based).
You will be mainly responsible for conducting global and local literature screening and assuring compliance with local and regional Quality Management System and exchange relevant safety and pharmacovigilance information.
This is full time employment position, the role is open for candidates from any EU/EEA Countries. All CVs must be submitted in the English language for consideration.
Pharmacist or Medical Doctor degree
2-year experience in Literature Screening for Pharmacovigilance
Fluent in English and Japanese languages
Computer literacy (MS Office), experience with PV databases
Strong organizational and time management skills
Ability to work independently and in a team
Responsibilities:
Ensure weekly monitoring of local and global literature review
Communicate with Health Authorities
Ensure compliance with applicable local guidelines and regulations
Collect, process, and communicate of safety information, product quality complaints and medical device incidents
Maintain and establish quality standards for local pharmacovigilance activities
Participate in inspection and/or audits
Ensure the survey and monitoring of national pharmacovigilance regulations
Receive and handle medical information enquiries from patients and health care professionals
A complete spectrum of Clinical Research, Regulatory Affairs, Pharmacovigilance and Medical Information solutions.
Industry
Research Services
Company size
201-500 employees
Founded
2001
Headquarters
Kaunas
LinkedIn followers
41,232
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.
We keep our promises. Always.
Social media privacy policy: bit.ly/privacy-biomapas
Offices: K. Donelaicio str. 60, Kaunas, LT – 44248, LT · 16 Pirogova, Almaty, 050040, KZ · 3 Route de la Corniche, Biopole, Lausanne, Epalinges 1066 , CH · Zemlyanoi val str., № 9, Moscow, Moscow City 105064, RU · Ilia Chavchavadze avenue, N 60b, floor 8, flat N 28, Tbilisi, - 0162, GE
A complete spectrum of Clinical Research, Regulatory Affairs, Pharmacovigilance and Medical Information solutions.
Industry
Research Services
Company size
201-500 employees
Founded
2001
Headquarters
Kaunas
LinkedIn followers
41,232
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.
We keep our promises. Always.
Social media privacy policy: bit.ly/privacy-biomapas
Offices: K. Donelaicio str. 60, Kaunas, LT – 44248, LT · 16 Pirogova, Almaty, 050040, KZ · 3 Route de la Corniche, Biopole, Lausanne, Epalinges 1066 , CH · Zemlyanoi val str., № 9, Moscow, Moscow City 105064, RU · Ilia Chavchavadze avenue, N 60b, floor 8, flat N 28, Tbilisi, - 0162, GE