Safety Surveillance Specialist for Global Safety. HOVEDSTADEN
Contrato de Médicos generales en HOVEDSTADEN (Dinamarca)
Clasificación del trabajo:Profesionales científicos e intelectuales : Profesionales de la salud : Médicos : Médicos generales. Arbejde, der forudsætter viden på højeste niveau inden for pågældende område : Arbejde inden for sundhedsområdet : Lægearbejde : Alment lægearbejde.
Descripción de la oferta de trabajo:
-?Pharmacovigilance -?Denmark - Bagsværd Do you like to be a driving force in ensuring highest safety and lowest possible risk to patients that use Novo Nordisk diabetes products? And would you like to be part of and set directions for one of the most skilled and advanced safety functions in Denmark? We are looking to strengthen our team with the knowledge and expertise a Medical Doctor (MD) will bring. If you find this challenging you may be our new colleague in Safety Surveillance. About the department Safety Surveillance is a department within Global Safety and is situated in Bagsværd, Denmark. Global Safety is an organisation of more than 400 highly professional people with a high level of educational background within natural science. Safety Surveillance has the global responsibility for the surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development worldwide. The position With a background as Medical Doctor, your primary responsibility is signal detection and management which includes the critical analysis and medical evaluation of the emerging safety data from clinical trials, marketed use, published literature and regulatory databases. You will be responsible for understanding the product safety profile and developing and maintaining the reference safety information and the labelling for Novo Nordisk products. You will also be responsible for communication about the benefit-risk assessment (PSUR, DSUR and RMP) and you will be our safety representative in cross-functional teams. Furthermore, you will play an important role in the development of clinical trial protocols and clinical trial reports where you with your expertise will provide medical/clinical input on collection and assessment of safety information. Your job responsibilities will also include chairing a cross-functional safety committee and communication with external parties related to clinical safety monitoring such as Data Monitoring Committees. As a Medical Doctor, you will bring broad and in depth understanding of medical concepts, disease processes also outside your area of speciality or specific therapeutic areas. With your medical background, you are expected to be a medical expert when interacting with internal and external stakeholders, cross functional area in HQ, teams in affiliates and health authorities. You will get the opportunity both to work independently and in collaboration with a team of highly skilled, committed and enthusiastic colleagues. Assuming responsibility, communicating information and taking action will be essential parts of your work day. You will have a close collaboration and interaction with other functional areas in Novo Nordisk especially Clinical Development and Regulatory Affairs and you will be an important contributor in the Novo Nordisk organisation. Qualifications For this position you will need to have a Medical Doctor degree together with solid experience within pharmacovigilance or extensive experience from clinical development and strong urge to specialise within pharmacovigilance. You have a solid understanding of diagnostic processes, diagnostic techniques and interpretation of diagnostic results. Furthermore, you have the ability to evaluate impact and consequences of disease condition and medical interventions. As a person you are ethical, responsible, well-organised and a strong communicator. You are able to work under pressure when needed and able to make independent decisions regarding drug safety issues. You thrive in a multicultural environment of continuous development, and you are good at establishing contact and firm in collaborating and communicating with stakeholders. You are a strong driver and a dedicated team player who enjoy supporting your non MD colleagues and also in challenging your MD colleagues. You are fluent in English both written and spoken (company language) and an experienced user of MS Office. Working at Novo N
Servicio de empleo de origen:AMS, Servicios Públicos de Empleo, Dinamarca.