Pharmacovigilance Specialist

Job SummaryWe are seeking a highly skilled Pharmacovigilance Specialist to join our team at Tevapharm. As a Pharmacovigilance Specialist, you will be responsible for performing pharmacovigilance activities within our PV Americas Operations Hub.Key ResponsibilitiesTriaging of adverse event information, including extraction, upload, and triage of XMLs.Case...

Job Title: Pharmacovigilance CoordinatorGalderma is a leading dermatology company with a strong presence in approximately 90 countries. We are committed to delivering innovative, science-based solutions that meet the evolving needs of consumers, patients, and healthcare professionals.We are seeking a highly skilled Pharmacovigilance Coordinator to join our...

About the OpportunityWe are seeking a skilled Pharmacovigilance Associate to join our team at Teva Pharmaceuticals. This is an exciting opportunity to work in a dynamic environment and contribute to the safety and well-being of patients.Your Experience and QualificationsTo be successful in this role, you will have a Bachelor's degree in a relevant field,...

About the OpportunityWe are seeking a skilled Pharmacovigilance Associate to join our team at Teva Pharmaceuticals. This is an exciting opportunity to work in a dynamic environment and contribute to the safety and well-being of patients.Your Experience and QualificationsTo be successful in this role, you will need a Bachelor's degree in a relevant field,...

Job Summary:As a Senior Pharmacovigilance Reporting Associate at ICON plc, you will play a critical role in ensuring the quality and integrity of pharmacovigilance reports. This position requires a strong understanding of pharmacovigilance regulations and guidelines, as well as excellent analytical and communication skills.About ICON plc:ICON plc is a...

Job OverviewThis role involves applying your knowledge and expertise to review, assess, and process Safety data across various service lines. You'll be recognized as a specialist in one or more areas, oversee small to medium operational projects, and mentor junior staff members.Key ResponsibilitiesProcess Safety data as per regulations, guidelines, SOPs, and...

Job Overview As a Pharmacovigilance Specialist at IQVIA, you will play a critical role in ensuring the safety and efficacy of pharmaceutical products in clinical trials. Under moderate supervision, you will execute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project...

Job OverviewAs a key member of our team at IQVIA, you will play a critical role in ensuring the safe and effective use of pharmaceutical products. Under moderate supervision, you will execute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or...

Job OverviewUnder moderate supervision, executes the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level for IQVIA.Key ResponsibilitiesExecute pharmacovigilance processes applicable to research sites.Submit safety reports (periodic...

About the OpportunityWe are seeking a highly skilled Pharmacovigilance Associate to join our team at Teva Pharmaceuticals. As a key member of our Pharmacovigilance team, you will play a critical role in ensuring the safety of our products and maintaining compliance with regulatory requirements.Your Experience and QualificationsTo be successful in this role,...

About the RoleSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we...

Job OverviewThis role involves applying your knowledge and expertise to review, assess, and process Safety data across various service lines. You'll be recognized as a specialist in one or more areas, oversee small to medium operational projects, and mentor junior staff members.Key ResponsibilitiesProcess Safety data as per regulations, guidelines, SOPs, and...

About the RoleWe are seeking a highly skilled Case Handling Specialist to join our team at Novo Nordisk. As a key member of our Global Business Service Centre, you will play a critical role in maintaining a high level of knowledge of safety database systems, reporting tools, SOPs, and regulatory guidelines to ensure adherence and compliance.Key...

Senior Pharmacovigilance Reporting Associate - Mexico, Mexico CityICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.What ICON can offer you:Our success...

Job OverviewAs a key member of the IQVIA team, this role will be responsible for executing the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level.Key ResponsibilitiesEnsure compliance with pharmacovigilance processes applicable to...

About the RoleWe are seeking a highly skilled Medical Science Liaison Specialist to join our team at Chiesi Farmaceutici. As a Medical Science Liaison Specialist, you will play a critical role in providing scientific and medical support to healthcare professionals, key opinion leaders, and academic centers in Mexico.Main ResponsibilitiesScientific and...

Job Title: Regulatory Affairs CoordinatorCompany: Fenixfarma Mexico City, MexicoJob Summary:We are seeking a highly skilled Regulatory Affairs Coordinator to join our team in Mexico City. The successful candidate will be responsible for ensuring compliance with local health regulations and leading a team of regulatory specialists to achieve product...

About ICON PlcICON Plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.What We OfferCompetitive SalaryRange of Health Insurance OfferingsCompetitive Retirement...

About the RoleWe are seeking a highly skilled Patient Safety Senior Associate to join our Clinical, Medical & Regulatory department at Novo Nordisk. As a key member of our team, you will be responsible for ensuring the safety and efficacy of our products by collecting and analysing safety information.Key ResponsibilitiesReceipt, documentation, triage and...

Job SummaryMedpace, Inc. is a leading full-service clinical contract research organization (CRO) seeking a highly skilled Clinical Safety Coordinator to join our team. This role plays a critical part in the pharmacovigilance process, ensuring the safe and effective development of medical therapeutics.Key ResponsibilitiesOversee the submission of safety...