Clinical Safety Specialist with Pharmacovigilance Expertise

Company OverviewPrime Vigilance Ltd is a specialized pharmacovigilance service provider established in 2008. With organic growth year after year, the company has achieved global recognition for its services in Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance. Job DescriptionThe Clinical Pharmacovigilance Specialist will be...

Job Overview: PrimeVigilance is seeking a highly skilled Clinical Pharmacovigilance Specialist to join our team in global operations.About the Role: As a key member of our PV team, you will be responsible for reviewing and approving post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials. You...

Established in 2008, PrimeVigilance has grown organically year after year to become a leading provider of pharmacovigilance services. As a global company with staff across Europe, North America, and Asia, we cover a range of services including Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance.We value our relationships with...

About SandozSandoz, a leading generic and biosimilar medicines company, has the opportunity to shape the future of healthcare. Our innovative production sites, acquisitions, and partnerships enable us to provide low-cost, high-quality medicines sustainably.Why Work at Sandoz?At Sandoz, we value diversity and inclusion. Our agile and collegiate environment...

Job OverviewWe are seeking a highly skilled Medical Safety Specialist to join our team at PrimeVigilance. As a Medical Safety Specialist, you will play a crucial role in reviewing and approving post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment.Key...

About SandozSandoz is a leading global generic and biosimilar medicines company, with a mission to pioneer access for patients. With a presence in almost 140 countries, our products touch the lives of nearly 500 million patients every year.We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients...

Job DescriptionAs a Clinical Document Specialist at PrimeVigilance Ltd, you will be responsible for creating and reviewing high-quality clinical documents. Your expertise in pharmacovigilance medical writing will help us maintain our reputation as a leading provider of drug safety services.About the RoleAuthor, edit, and review regulatory/clinical documents,...

About the Company">We are PrimeVigilance, a leading pharmacovigilance service provider with global reach and expertise. Our team of professionals is dedicated to delivering high-quality support to pharmaceutical and biotechnology partners across various therapy areas.At PrimeVigilance, we prioritize diversity, equity, and inclusion by creating an equal...

Job DescriptionJob Title: Pharmacovigilance SpecialistJob Summary:We are seeking a highly skilled Pharmacovigilance Specialist to join our team at Organon. As a key member of our Pharmacovigilance department, you will be responsible for ensuring the safe and effective use of our products.Responsibilities:Manage adverse event cases from receipt to closure in...

About IQVIAIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.Job DescriptionThis role will put you at the...

Job OverviewPrimeVigilance is seeking a highly skilled Clinical Review Specialist to join our team. As a Clinical Review Specialist, you will play a vital role in ensuring the safety of patients by reviewing and approving post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical...

Job DescriptionOrganón is seeking a highly skilled Pharmacovigilance Specialist to join our team. The ideal candidate will have a strong background in pharmacovigilance and regulatory affairs.Responsibilities:Manage day-to-day adverse events case management, including case intake and follow-up activities in accordance with Global Pharmacovigilance...

Job DescriptionWe are seeking a highly skilled Pharmacovigilance Specialist to join our team at Organon. The ideal candidate will have a strong background in pharmacovigilance and regulatory affairs, with excellent communication and time management skills.ResponsibilitiesManage day-to-day adverse events case management, including case intake and follow-up...

Job SummaryWe are seeking a highly skilled Pharmacovigilance Specialist to join our team. The ideal candidate will have a strong background in pharmacovigilance and regulatory affairs, with a minimum of 1 year of industry experience.Key ResponsibilitiesManage day-to-day adverse events case intake and follow-up activities in accordance with Global...

Job SummaryJoin IQVIA's team of medical information specialists and contribute to the development and commercialization of innovative medical treatments.We are seeking a highly skilled Medical Information and Adverse Event Intake Specialist with expertise in Italian and English languages to support our global safety operations team.ResponsibilitiesProvide...

**Job Summary**Organon is seeking a highly skilled Drug Safety Specialist to join our team. As a key member of our Pharmacovigilance team, you will be responsible for managing adverse event cases, ensuring compliance with global and local regulations, and providing support for patient safety initiatives.**Key Responsibilities**Manage day-to-day adverse event...

About UsAt Sandoz, we strive to make a meaningful difference in the lives of millions of patients worldwide. Our commitment to innovation and quality has made us a leader in the global medicines industry.We are proud to have touched the lives of almost 500 million patients last year and we're eager to continue our mission of providing low-cost, high-quality...

Explore a rewarding career opportunity at Organon, a leading global healthcare company dedicated to improving women's health and well-being.About the RoleWe are seeking an experienced Medical Safety Professional with expertise in pharmacovigilance to join our team. As a key member of our safety organization, you will be responsible for ensuring compliance...

Safety Oversight and ExpertiseWe are seeking a Medical Safety Director to provide medical, scientific, and therapeutic expertise on pharmacovigilance services. As a key member of our team, you will participate in all aspects of Medical Safety activities, including reviewing and clarifying trial-related Adverse Events, and providing medical evaluation of...

At Iqvia Llc, we are seeking a Medical Information and Safety Specialist to join our team. As a key member of our Lifecycle Safety Operations team, you will play a crucial role in designing, building, and executing end-to-end safety solutions for major pharmaceutical companies.As a Medical Information and Safety Specialist, your primary responsibility will...