- Chair cross-functional drug safety committees.
- Prepare communication about the benefit risk assessment.
- Contribute to development of clinical study designs and protocols.
- Communicate with external parties related to clinical safety monitoring such as Data Monitoring Committees.
- Represent Safety Surveillance in cross-functional teams.
- A Master's degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent), possibly complemented by a PhD/research experience
- Preferably several years of experience within pharmacovigilance, or within the pharmaceutical industry and a strong desire to specialise within safety surveillance
- Interest/experience in data analysis and analysis tools (e.g.Jmp and/or Qliksense)
- A solid understanding of medical concepts, scientific methodology, and drug development
- Curiosity to explore new ways of analysing data (e.g. could be in the form of optimizing current ways of working)
- The ability to work independently as well as to collaborate in a continuous developing environment
-
Rare Disease
for 1 uge siden
Novo Nordisk Søborg, DanmarkDo you want to lead and drive safety surveillance activities in development projects in rare diseases? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark? · We are expanding and therefore have open positions for experienc ...
-
Clinical Medical Director
for 1 uge siden
TFS HealthScience Søborg, Danmark FuldtidAre you passionate about making a difference in the lives of patients with rare oncology diseases? Join our innovative team at TFS HealthScience as we expand our horizons and contribute to groundbreaking advancements in healthcare. · This position is sponsored-based in Sweden, bu ...
-
Clinical Project Lead
for 5 dage siden
Novo Nordisk Søborg, DanmarkThe job · is based in Søborg in Denmark but has a global scope. Some international travelling may be part of the job. Qualifications You will be a great asset to our team because you have: MSc in Natural, Health or Pharmaceutical Science with at least five years of relevant expe ...
-
Clinical Operations Lead
for 4 dage siden
Novo Nordisk Søborg, DanmarkThe position · We are looking for a Clinical Operation Leads in all our 5 areas. In this position, you take on a senior role with extensive responsibilities, being accountable for all aspects of the operational start-up and initiation activities of a clinical trial. Your main re ...
-
Global Portfolio Director
for 1 uge siden
Novo Nordisk Søborg, DanmarkThe position · As Global Portfolio Director, you will join a team dedicated to delivering top-quality quantitative and qualitative commercial assessments. Your responsibilities, focused on rare diseases and stem-cell based therapies, will include: Working within a drug candidate ...
-
Senior Clinical Project Manager
for 1 uge siden
TFS HealthScience Søborg, Danmark FuldtidJoin our innovative team at TFS HealthScience as we continue our commitment to advancing clinical research and improving patient outcomes. We are currently seeking a talented Senior Clinical Project Manager to lead clinical studies and drive the development of life-changing treat ...
-
Senior UX/UI Designer
for 4 dage siden
Novo Nordisk Søborg, DanmarkThe position · is in the Digital Accelerator, a fast moving and highly skilled department helping Novo Nordisk in green field software development. We are currently + people, with 20 experienced UX/UI colleagues. We are 18 nationalities and support diversity in all aspects. We a ...
-
Director of Clinical Trial Simulations
for 6 dage siden
Novo Nordisk Søborg, DanmarkThe position · will be based in either Søborg (Denmark) or the East Coast (US). Qualifications To be successful in this role, we are looking for a candidate with the following qualifications: Extensive experience in the pharmaceutical, biotech, or healthcare industry. A strong m ...
-
APMO Coordinator
for 1 uge siden
Novo Nordisk Søborg, DanmarkThe job · is an ideal entry position, and applications from newly graduated are welcomed. If you graduate this summer, you are also welcomed to apply, and we will adapt the starting date to your availability. You will receive the needed training, certification and introduction t ...
-
APMO Coordinator
for 3 dage siden
Novo Nordisk A/S Søborg, Danmark. · Want to start your career as Agile Project Management Office Coordinator and work with data and IT in an agile setting? Do you have a mindset of always improving the way we work and enhancing our efficiency? · Then read-on. Apply today · About Development IT · You will be pa ...
-
Manager of Safety Surveillance Early Development
for 1 uge siden
Novo Nordisk A/S Søborg, DanmarkDo you want to play a key role in driving the ongoing safety surveillance activities for early development projects in Novo Nordisk? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark, setting direction and inspiring a tea ...
-
APMO Coordinator
for 1 uge siden
Novo Nordisk A/S - VTx Søborg, Danmark Fuldtid.Want to start your career as Agile Project Management Office Coordinator and work with data and IT in an agile setting? Do you have a mindset of always improving the way we work and enhancing our efficiency? · Then read-on. Apply today About Development IT · You will be part of ...
-
Director of Clinical Trial Simulations
for 6 dage siden
Novo Nordisk A/S Søborg, DanmarkAre you prepared to be a game-changer in drug development? Do you possess the leadership and the technical expertise to refine clinical drug development through the power of clinical trial simulations? If so, we invite you to join our dynamic Pharmacometrics team at Novo Nordisk. ...
-
Scrum Master
for 3 dage siden
Novo Nordisk Søborg, Danmark- · We are looking for a passionate Scrum Master who is dedicated to agile ways of working and is energized by building software that makes an impact: for developers, for users and for the patients of Novo Nordisk. Do you thrive within an environment of co-creation, entrepreneurs ...
-
Director of Clinical Trial Simulations
for 3 dage siden
Novo Nordisk Søborg, DanmarkAre you prepared to be a game-changer in drug development? Do you possess the leadership and the technical expertise to refine clinical drug development through the power of clinical trial simulations? If so, we invite you to join our dynamic Pharmacometrics team at Novo Nordisk. ...
-
Manager of Safety Surveillance Early Development
for 1 uge siden
Novo Nordisk Søborg, DanmarkDo you want to play a key role in driving the ongoing safety surveillance activities for early development projects in Novo Nordisk? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark, setting direction and inspiring a tea ...
-
Environmental and HVAC Supporter
for 2 dage siden
Novo Nordisk A/S Gentofte, DanmarkAre you a professional with a passion for HVAC and environmental support? Would you like to help us set direction and drive interesting projects? Do you dream about supporting patients with rare and serious chronic diseases? · Then you might be our new Environmental and HVAC Sup ...
-
Digital Change Consultant
for 1 uge siden
Novo Nordisk A/S Gentofte, DanmarkAre you passionate about driving digital transformation activities focusing on the human side? Do you want to support projects within change, culture and learning across the Biotech & Rare Disease (BRD) value chain? Do you have experience in facilitating workshops and driving awa ...
-
Rigshospitalet - Blegdamsvej Hellerup, Danmark LægeEn uklassificeret reservelægestilling ved Afdeling for Hjerne- og Nervesygdomme, Rigshospitalet – Blegdamsvej er ledig til besættelse 1. september 2024 eller snarest derefter. Stillingen er velegnet som supplerende klinisk erfaring inden hoveduddannelse. · Om klinikken · Afdelin ...
-
Aseptic Supporter
for 1 dag siden
Novo Nordisk A/S Gentofte, DanmarkAre you motivated by the pulse of a GMP production area? Are you eager to work in a team that drives optimization of process and equipment related to aseptic filling process? · If yes, we are currently seeking a new highly motivated colleague to join our Aseptic Support Team in G ...
Rare Disease - Søborg, Danmark - Novo Nordisk A/S
Beskrivelse
Do you want to lead and drive safety surveillance activities in development projects in rare diseases? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark?
We are expanding and therefore have open positions for experienced candidates in the Safety Surveillance Rare Disease team at Novo Nordisk.
Apply today for a life-changing career
About the Teams
Safety Surveillance Rare Disease is a team within Global Safety at Novo Nordisk. Our dedicated and skilled professionals have global responsibility for the establishment of the product safety profile during clinical development, and for performing critical analysis and medical evaluation of the emerging aggregate safety data. Due to an increase in the number of development projects, our team is expanding.
In the Rare Disease team, we handle projects within the rare disease indication from development to post marketing. You will in collaboration with other colleagues in the team, be responsible for surveillance activities related to the compounds in development for rare blood and bleeding disease indications.
The Position
Responsibilities may include:
You will get the opportunity both to work independently and in collaboration with a team of highly skilled, committed, and enthusiastic colleagues across the functional areas in Novo Nordisk, especially the Non-clinical and Clinical Development teams. Assuming responsibility, communicating information and taking action will be essential parts of your workday.
Qualifications
As an ideal candidate, you will have:
It is important that you are a strong collaborator who thrives in a multicultural environment of continuous development, and that you are good at establishing contacts and collaborating with stakeholders out in the organisation as well as external stakeholder's.
As a person, you are self-driven and able to work independently and under pressure when needed. You are ethical, responsible, well-organised and a strong communicator.
