Manager, Global Drug Safety

We are seeking a highly skilled (Senior) Manager, Safety Data Management, to join our Global Drug Safety and Pharmacovigilance (GDS&PV) unit. As a key member of our team, you will be responsible for configuring and maintaining safety systems, generating complex reports, and implementing and validating safety systems and solutions. Your expertise in safety...

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 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...

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...

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...

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...

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...

```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...

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 Description:We are seeking a skilled CMC Project Manager to lead our team in the development of new drugs. As a key member of our Global CMC-Development team, you will be responsible for managing projects from pre-clinical to clinical phases and ensuring timely delivery of high-quality results.About the Role:You will work closely with cross-functional...

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...

Digital Marketing Role at RelyOnWe are RelyOn, a global business delivering safety, compliance, and competence services and solutions around the world. Our mission is to help clients protect their people, assets, and the environment.We are seeking a Marketing and Communications Specialist to join our Global Marketing team in Copenhagen. The successful...

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 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...

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...

Job OpportunityWe're seeking a seasoned Clinical Drug Supply Manager to join our team in Copenhagen, Denmark or Princeton, New Jersey.This position requires a strong background in cGMP and a focus on delivering high-quality results.About the JobManage the coordination of drug supply and provide IMPs for clinical trials, IST, and PAA programs.Develop and...

Job DescriptionWe are seeking an experienced IT Safety Solutions Expert to join our team at Novo Nordisk. The ideal candidate will have a strong background in health and safety IT solutions and project management.About the RoleAs a Health & Safety IT Solution Specialist, you will be responsible for driving the planning, facilitation, and execution of pivotal...

About Our Ideal CandidateOur ideal candidate is a natural leader who is just as comfortable setting strategy as they are jumping in to execute it.They have some experience in safety/risk management, preferably in consumer-facing businesses or technology platforms, and a passion for data-driven insights to make informed decisions.Key qualities we're looking...