Global Regulatory Associate

Join our dynamic Nordic Regulatory Affairs team as a Regulatory Affairs Associate! As a key member of our team, you will play a critical role in ensuring compliance with regulatory requirements and maintaining high standards of quality.About This RoleThis role involves supporting Global Regulatory Affairs applications, creating and updating product...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

At Eli Lilly and Company, we are a global healthcare leader committed to improving the lives of people around the world. We unite caring with discovery to bring life-changing medicines to those who need them.About This RoleThis exciting opportunity is part of our Nordic Regulatory Affairs team, encompassing a broad range of regulatory activities across the...

Eli Lilly and Company is seeking a highly motivated and detail-oriented Global Regulatory Affairs Associate to join our Nordic Countries team. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring compliance with regulatory requirements and maintaining high standards of quality.About This RoleThis role involves...

What We're Looking ForWe're seeking a highly motivated and organized individual to join our team as a Regulatory Affairs Associate. You'll need to have a relevant Bachelor's Degree or higher and 2+ years of related regulatory experience.You should have knowledge of the consumer healthcare environment and product development, as well as effective time and...

Job OverviewWe are seeking a highly skilled Regulatory Expert with experience in start-up activities to join our team in Solna, Sweden. As a Regulatory and Start-Up Specialist 2, you will be responsible for performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international...

Overview:We are seeking a highly skilled and experienced Clinical Study Manager to oversee several clinical studies regulated by the FDA and EMA. The successful candidate will ensure compliance with protocols, Valneva SOPs, Good Clinical Practice (GCP), and relevant regulatory requirements.Key Qualifications:Master's Degree in Life Science or equivalent...

We're looking for a highly skilled Regulatory Compliance Specialist to join our team in Sweden and Norway. As a key member of our Nordic Regulatory Affairs team, you will play a critical role in ensuring compliance with regulatory requirements and maintaining high standards of quality.About This RoleThis role involves supporting Global Regulatory Affairs...

Social network you want to login/join with:Regulatory and Start Up Specialist 2 (FSP) Sweden, SolnaClient:IQVIALocation:Solna, SwedenJob Category:OtherEU work permit required:YesJob Reference:63216d880303Job Views:8Posted:15.03.2025Job Description:Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with...

Social network you want to login/join with:Manager Regulatory Affairs Nordics, SolnaClient: Kenvue Brands LLCLocation: Solna, SwedenJob Category: OtherEU work permit required: YesJob Reference: fc95f0c2f8beJob Views: 4Posted: 19.04.2025Expiry Date: 03.06.2025Job Description:Description Kenvue is currently recruiting for: Regulatory Affairs Manager Nordics...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Key Responsibilities:Permitting & Regulatory Compliance: Obtain, renew, and ensure compliance with all necessary permits, licenses, and regulatory approvals in Vietnam, securing timely success.Public Affairs & Government Relations: Establish strong relationships with government agencies, policymakers, and industry associations to influence favorable...

Vattenfall is one of Europe`s largest electricity generators and producers of heat. We operate in Sweden, Denmark, Germany, the Netherlands and the UK and are looking into European market opportunities. Our strategy is to reduce emissions from power generation with a road map aiming at achieving climate neutrality by 2050.The Business Unit Solar & Batteries...

Clinical Trial Assistant Job Summary">The Clinical Trial Assistant will provide administrative support to the Clinical Research Associates and Regulatory and Start-Up teams to ensure the successful execution of clinical trials.">Key Duties and Responsibilities">Provide administrative support to CRAs and RSU with updating and maintaining clinical documents...

About the Role">As a Clinical Trial Assistant at IQVIA, you will play a crucial role in ensuring the successful execution of clinical trials. The primary responsibility of this position is to provide administrative support to the Clinical Research Associates and Regulatory and Start-Up teams.">Key Responsibilities">Assist CRAs and RSU with updating and...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Job SummaryThe Public Affairs and Permits Manager will oversee regulatory compliance, secure necessary permits, and manage relationships with government agencies, industry associations, and key stakeholders in Vietnam. This role is essential for ensuring smooth business operations and advocating for favorable policies.

Clinical Trial Operations Assistant">This role supports the Clinical Research Associates and Regulatory and Start-Up teams to ensure the successful execution of clinical trials.">Key Responsibilities">Support CRAs and RSU with maintaining clinical documents and systems.Prepare and handle clinical documentation and reports according to standard operating...

About YouTo succeed in this role, you should have experience in regulatory affairs, energy policy, or related fields, ideally with a focus on German energy markets and renewables. Previous engagement with regulatory bodies or lobbying activities is a plus.A Bachelor's or Master's degree in Law, Economics, Energy Policy, Environmental Studies, or a related...

At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world's most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and...