Senior Manager, Drug Safety and Pharmacovigilance

At Genmab, we're committed to building extraordinary futures together, by developing antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. Our people are caring, candid, and impact-driven, and our business is innovative and rooted in science. We believe that being proudly unique,...

Select how often (in days) to receive an alert: Create Alert Category: Reg Affairs & Safety Pharmacovigilance Location: Ørestad, Capital Region of Denmark, DK Are you passionate about ensuring patient safety and compliance in pharmacovigilance? Do you have a knack for strategic oversight and collaboration across international teams? We are looking for a...

About GenmabGenmab is an international biotech company specializing in the invention and development of differentiated human antibody therapeutics for the treatment of cancer and other important human diseases. We are committed to building extraordinary futures together and transforming the lives of patients through innovative cancer treatment.The RoleAs a...

About GenmabWe are an international biotechnology company committed to developing antibody products and pioneering therapies that transform the lives of patients with cancer and other serious diseases. Our team is driven by a passion for innovation, excellence, and collaboration.The RoleAs a Senior Manager, Safety Data Management, you will join our Global...

About UsAt Genmab, we're committed to building extraordinary futures together, by developing antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. Our people are caring, candid, and impact-driven, and our business is innovative and rooted in science.The Job DescriptionThis role...

About UsGenmab is an international biotechnology company that specializes in the invention and development of innovative antibody therapeutics for the treatment of cancer and other important human diseases.The RoleAs a (Senior) Manager, Safety Data Management, you will join our Global Drug Safety and Pharmacovigilance (GDS&PV) unit, where you will be...

About the RoleThis is an exciting opportunity for a seasoned leader to join LEO Pharma as a Global Safety Surveillance Manager. As part of our Global Safety Surveillance department, you will lead a team of Global Safety Advisors and Safety Leads, ensuring compliance with pharmacovigilance processes, regulations, and guidelines. If you have a passion for...

Role OverviewLeverage your expertise in pharmacovigilance and safety data management to drive compliance and maintain high standards in adverse event case management. As a Global Safety Specialist at LEO Pharma, you will play a critical role in ensuring the processing and distribution of adverse event cases.Key ResponsibilitiesConduct thorough case triage...

Job DescriptionThe successful candidate will be responsible for ensuring compliance with local legislations, safety data exchange agreements, and global ICSR regulations. This role requires a strong understanding of pharmacovigilance principles and experience in managing adverse event cases.Key Skills and QualificationsPharmacovigilance and/or safety data...

Safety Data Management RoleThis role offers a unique opportunity to apply your knowledge and skills in pharmacovigilance and safety data management to drive excellence in adverse event case management. As a Global Safety Specialist, you will be part of a dynamic team focused on ensuring compliance and maintaining high standards in safety operations.Your Key...

Job OverviewThe role of the Global Safety Surveillance Manager at LEO Pharma involves leading a team of experts to ensure compliance with pharmacovigilance processes, regulations, and guidelines. The successful candidate will have strong leadership skills, experience in project-oriented environments, and a deep understanding of global regulatory...

Lundbeck A/S, H is a Danish pharmaceutical company that develops innovative treatments for brain disorders. As a Senior Research Scientist, you will join the Department of Drug Metabolism within the Non-Clinical Safety Research division.Your key responsibilities will involve evaluating the drug-drug interaction risk of Lundbeck development compounds,...

```html The position As a Director for the Safety Surveillance Office, you will be part of the Safety Surveillance leadership team and Council and will report to the head of Safety Surveillance. The area has expanded significantly over the last few years, and we are therefore looking for a director to head up the new department to further strengthen and...

Lundbeck A/S, H is a Danish pharmaceutical company that develops innovative treatments for brain disorders. As a Principal Investigator, you will lead the Department of Drug Metabolism within the Non-Clinical Safety Research division.Your primary responsibilities will involve evaluating the drug-drug interaction risk of Lundbeck development compounds,...

At Genmab, we're committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in...

Do you want to play an essential role in ensuring drug product quality throughout its lifecycle and in supporting Novo Nordisk's production of high quality, world-leading diabetes and obesity products? Are you motivated by cross team collaboration, driving optimization and ready to change the game together with colleagues in a dynamic department? Then this...

Job DescriptionWe are seeking an experienced professional to join our Global Safety Surveillance department as a Manager. In this role, you will be responsible for leading a team of Global Safety Advisors and Safety Leads, ensuring compliance with pharmacovigilance processes, regulations, and guidelines. As a key member of our team, you will have the...

Do you have a passion for LC-MS and like to work with "state of the art" technologies? Do you thrive with scientific challenges? Then you may be our new colleague. Your new role – why is this a great opportunity? You will be responsible for planning, conducting, and reporting of in vitro and in vivo ADME studies, including metabolite profiling and...

Job SummaryWe're looking for a skilled Clinical Drug Supply Manager to join our team in Copenhagen, Denmark or Princeton, New Jersey.This role involves managing clinical trial supplies, collaborating with CMOs, and ensuring compliance with quality standards.About the TeamYou'll be part of a highly competent team focused on packaging and labeling of supplies...

At Genmab, we're committed to building extraordinary futures together, by developing antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being...