Regulatory Affairs Specialist

Job OverviewSyneos Health is a leading provider of biopharmaceutical solutions, dedicated to accelerating customer success through clinical, medical affairs, and commercial insights.We are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory department, you will be responsible for ensuring compliance with...

Medison is a global pharma company providing access to highly innovative therapies to patients in international markets. Medison commercializes highly innovative therapies across international markets, helping to save and improve the lives of patients suffering from the most challenging diseases. Medison is rapidly growing in the international markets backed...

OverviewTakeda is a pharmaceutical company committed to improving the lives of patients worldwide through innovative and groundbreaking treatments. We are seeking an experienced Regulatory Affairs Expert to join our team, playing a pivotal role in shaping regulatory strategies that ensure timely and successful product approvals.About the RoleThe ideal...

Company OverviewIQVIA 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...

About IQVIA ArgentinaIQVIA 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.Job DescriptionThe Regulatory Affairs Specialist will...

Job Title: Regulatory Affairs AnalystNovo Nordisk A/S is a global leader in the development and manufacturing of innovative pharmaceuticals. We are currently seeking a talented Regulatory Affairs Analyst to join our team in Argentina.About the RoleThis is an exciting opportunity to work in a dynamic and professional environment where you will be responsible...

Select how often (in days) to receive an alert: Create AlertCategory: Reg Affairs & Safety PharmacovigilanceLocation: Vicente Lopez, Buenos Aires, ARAre you passionate about regulatory compliance?Do you want to play a crucial role in ensuring the licence to operate in Argentina?We are looking for a dedicated Regulatory Affairs Analyst to join our team in...

Join Novo Nordisk A/SWe are a leading global healthcare company with a strong legacy in the pharmaceutical industry. Our mission is to drive change to defeat serious chronic diseases and improve patient lives.Regulatory Affairs Analyst Job SummaryThis is an exciting opportunity to work in a dynamic and professional environment where you will be responsible...

Job SummaryWe are seeking a highly skilled Global Regulatory Lead Specialist to join our team at Takeda. As a key member of our regulatory affairs department, you will play a vital role in driving regulatory success and ensuring compliance with applicable requirements.Your primary responsibilities will include:Developing and implementing area regulatory...

Company OverviewNovo Nordisk A/S is a leading global healthcare company with a strong legacy in the pharmaceutical industry. Our mission is to drive change to defeat serious chronic diseases and improve patient lives.Job DescriptionWe are seeking a highly skilled Regulatory Affairs Analyst to join our team in Argentina. As a Regulatory Affairs Analyst, you...

Job Description: Tether Operations Limited is seeking a Regulatory Affairs Administrator to support its operations. The ideal candidate will have excellent communication skills, be able to juggle multiple tasks, and possess strong organizational, critical thinking, and interpersonal skills.In this role, you will manage legal documents, schedule meetings,...

Job DescriptionAs a Regulatory Coordinator at Alimentiv Inc., you will play a vital role in ensuring the compliance of clinical trials with regulatory requirements. Your primary responsibility will be to assist with and/or complete submissions to Regulatory Authorities, Ethics Committees, and other review bodies.Key ResponsibilitiesSubmit documents related...

Job DetailsThe Regulatory Affairs Specialist will be responsible for ensuring the compliance and accuracy of regulatory information across various regions.This role involves working closely with the RA Lead, RA Labeling Lead, and GLLs (Global Labelling Leads) to ensure the success of various projects and initiatives.The specialist will also be responsible...

Job OverviewThe Regulatory Coordinator is responsible for ensuring the compliance of clinical trials with regulatory requirements. This involves working closely with the internal study team, sponsor, and external stakeholders to ensure timely and accurate submissions.Main ResponsibilitiesDevelop and maintain study regulatory trackersAuthor Submission...

Job DescriptionThe Regional Regulatory Specialist will be responsible for enabling Grundfos products & solutions to meet local compliance obligations with regards to all relevant compliance areas by obtaining and maintaining local approvals/certification across the region.Main Responsibilities:Secure efficient monitoring of new or changed product compliance...

Position DetailsThis Regulatory Affairs Specialist position requires experience in US labeling activities or local (own country or LATAM) labeling activities. The ideal candidate will be able to accurately distribute CCDS to relevant stakeholders and update the Regulatory Information System to capture submission due dates, deferred submission dates, and CCDS...

**Job Description**The Senior Compliance Officer will oversee adherence to local and international regulatory standards for Glencore's Argentinian companies (Pachon and MARA), promoting a culture of compliance within the organization. This critical role maintains our commitment to ethical business practices and risk mitigation.Responsibilities...

Job SummaryThe Regulatory Affairs Specialist will work closely with the RA Lead, RA Labeling Lead, and GLLs (Global Labelling Leads) to ensure the success of various projects and initiatives.This role involves managing the Regulatory Information System, updating submission due dates, and assisting with CCDS template/content transfers.The specialist will also...

IQVIA ArgentinaWe are seeking a talented Regulatory Start-Up Specialist to join our team in Argentina.About the Role:As a Regulatory Start-Up Specialist, you will be responsible for ensuring that all site activation activities are conducted in accordance with applicable regulations, SOPs, and project requirements.Key Responsibilities:Perform site activation...

Job OverviewThe Regulatory Start-Up Specialist will be responsible for performing tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual guidelines.Key Responsibilities:Under general supervision, serve...