Posted:
9/11/2024, 4:19:41 AM
Location(s):
Tartu, Estonia ⋅ Kaunas, Kaunas County, Lithuania ⋅ Riga, Latvia ⋅ Kaunas County, Lithuania
Experience Level(s):
Junior ⋅ Mid Level
Field(s):
Legal & Compliance
You will be responsible for regulatory activities required at a country level for medical devices and medicinal products, including maintenance and approvals, marketing authorization transfers, communication with the Health Authority, artwork approval etc. ensuring regulatory compliance in the applicable markets: Lithuania, Latvia, Estonia.
As part of the IQVIA Global Regulatory Affairs department, you will be working with our clients – global pharmaceutical companies.
Key Responsibilities
Qualifications
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
Website: https://iqvia.com/
Headquarter Location: Danbury, Connecticut, United States
Employee Count: 10001+
Year Founded: 1982
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Analytics ⋅ Health Care ⋅ Life Science