Experienced Safety Surveillance Specialists

1 month ago


Søborg, Denmark Novo Nordisk AS - VTx Full time

The position We are currently in the process of expanding our clinical activities and are seeking individuals to help lead a range of prestigious projects. We promise a dynamic and rewarding experience at a leading global healthcare company such as Novo Nordisk. As the position is based in Denmark and due to the specifics of the job that make it fully office-based, we highly encourage candidates who are ready to relocate to Denmark to apply. As an experienced Safety Surveillance Specialist, you will play a pivotal role in supporting the safety surveillance of products in both clinical development stages II & III. Key tasks include: Contribute to development of new drugs by using your medical/clinical expertise on collection and assessment of safety information and trial design Perform critical analysis and medical evaluation of the emerging aggregate safety data and contribute to establishment of the product safety profile during development Communicate information regarding the assessment of benefits and risks Represent Safety Surveillance in cross-functional teams Potentially chair the internal Novo Nordisk safety committee You will get the opportunity both to work independently and in collaboration with a team of highly skilled, dedicated, and enthusiastic colleagues. You will establish close partnership and interaction with other functional areas within Novo Nordisk, especially the Clinical Development and Regulatory Affairs teams, providing you with extensive insights into the entire Novo Nordisk value chain. Taking on responsibilities, sharing information, and taking proactive steps will be integral aspects of your daily tasks. Qualifications As an ideal candidate, you have: A University degree in Life Sciences (e.g., Pharmacy, Medicine, Veterinary or Biological); preferably complemented by a PhD Minimum of 5 years of experience within drug safety/pharmacovigilance or drug development Good understanding of medical concepts, disease processes, scientific methodology and data analysis Experience with clinical trial activities will be an advantage Strong IT skills and knowledge of computer systems including MS office Proficiency in English both written and spoken Your proactive approach, problem-solving nature, and team-player spirit are crucial for thriving in our fast-paced, multicultural environment of continuous development. It is essential that you possess strong collaboration abilities and excel at establishing effective communication with stakeholders. As a person, you demonstrate responsibility and high ethical and quality standards. About the department Safety Surveillance is a department within Global Safety and is situated in Søborg, Denmark. We also have a department in Bangalore, India. We are globally accountable for surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development. We additionally handle safety label updates, preparation of Risk Management Plans and aggregate reports. We treasure a positive and inclusive atmosphere in our team(s) and count on you to engage and participate in a positive manner as well. Working at Novo Nordisk At Novo Nordisk, we do not wait for change. We drive it. We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we are all working to move the needle on patient care.


  • Rare Disease

    1 month ago


    Søborg, Denmark Novo Nordisk AS Full time

    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. ...


  • Søborg, Denmark Novo Nordisk Full time

    The position is based in Søborg and weekly on-site presence is essential. For international candidates, relocation to Denmark is required. Qualifications As an ideal candidate, you have: A university degree in Life Sciences (e.g., Pharmacy, Medicine, Veterinary or Biological); preferably complemented by a PhD Several years of experience within drug...


  • Søborg, Denmark Novo Nordisk AS Full time

    Do 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 team of highly engaged professionals?  If so, you may be our new Department...


  • Søborg, Denmark Novo Nordisk Full time

       Do 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 team of highly engaged professionals? If so, you may be our new Department...


  • Søborg, Denmark Novo Nordisk Full time

    The position You will be responsible for leading a team consisting of dedicated safety surveillance advisers with medical and life science background. It will be your job to: Set direction for your team and contribute to quality improvement projects Lead and develop the people in your team Ensure safety contribution to the clinical and regulatory...


  • Søborg, Gladsaxe Municipality, Denmark Novo Nordisk AS - VTx Full time

    Are you ready to assume a key coordinating role for planning, conduct and follow-up on pharmacovigilance (PV) audits and inspections, working independently with a high degree of flexibility, high level of responsibility whilst influencing and co-operating with many different stakeholders, at all levels of the organisation? If you find challenges like this...


  • Søborg, Denmark Novo Nordisk AS Full time

    Do you want to contribute to the safety and quality of Novo Nordisk clinical development products? Would you like to use your medical knowledge to handle serious adverse events reported from clinical trials? Would you thrive in a well-regulated area where you make sure that global regulatory requirements are complied with? Then you might be the Associate...


  • Søborg, Denmark Novo Nordisk AS Full time

    Are you ready to assume a key coordinating role for planning, conduct and follow-up on pharmacovigilance (PV) audits and inspections, working independently with a high degree of flexibility, high level of responsibility whilst influencing and co-operating with many different stakeholders, at all levels of the organisation?  If you find challenges like...


  • Søborg, Denmark Novo Nordisk AS Full time

    Are you an inspirational leader who is passionate about people development and guiding others to achieve their goals? Do you want to influence how we safeguard Novo Nordisk patients?  Then you might be the ideal candidate for the position of Manager for one of our Safety Operations Case Management teams. Apply today and join us for a life-changing...


  • Søborg, Denmark Novo Nordisk Full time

    The position As Manager for one of the Case Management teams, your responsibilities will include: Day-to-day people management, performance, and development of employees within your team. Motivating and supporting employees through collaborative decision-making and ongoing prioritization. Playing an active role in setting direction for the team and...


  • Søborg, Denmark Novo Nordisk Full time

    The position is placed in the QPPV Office in Global Safety. Global Safety is globally responsible for handling of adverse events, monitoring product safety, customer complaints and potential recalls in Novo Nordisk. In QPPV Office we are around 50 colleagues with different professional background divided into different departments ensuring maintenance...


  • Søborg, Gladsaxe Municipality, Denmark Aeven AS Full time

    Advanced Quality Specialist (GxP) for our Application Lifecycle Management (ALM) TeamProfile Summary The Advanced Quality Specialist is responsible for ensuring the quality and compliance of the ALM Quality Center software, The Advanced Quality Specialist will perform various tasks related to validation, testing, release management, support, audit, training,...

  • QA/RA specialist

    1 month ago


    Søborg, Denmark Baxter Full time

    Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney...


  • Søborg, Gladsaxe Municipality, Denmark European Energy AS Full time

    Would it motivate you to work directly with renewable energy assets, ensuring that they operate to the best of their ability, thereby accelerating the green transition? As a Renewable Asset Management Specialist with European Energy, you have a chance to work with the Solar PV Systems in our international portfolio of assets, including improvement and...


  • Søborg, Denmark European Energy AS Full time

    Would it motivate you to work directly with renewable energy assets, ensuring that they operate to the best of their ability, thereby accelerating the green transition? As a Renewable Asset Management Specialist with European Energy, you have a chance to work with the Solar PV Systems in our international portfolio of assets, including improvement and...


  • Søborg, Denmark Novo Nordisk AS Full time

    Are you a Medical Doctor (MD) with a solid industry experience and curious about the opportunities at Novo Nordisk? Or you have substantial clinical and research experience – ideally within diabetes and are looking for new challenges? Then, take a look at the opportunities within our Diabetes area! The position We are searching for new passionate...


  • Søborg, Denmark Novo Nordisk Full time

    The position is in a production support department, GCM Support, a team of highly experienced professionals and specialists with a well-documented history in pharmaceutical sciences. You will join a team of experts within the field and become a part of a well-functioning team where we work and solve problems in collaboration. Several of the CMOs we...


  • Søborg, Denmark Novo Nordisk Full time

       Are you a Medical Doctor (MD) with a solid industry experience and curious about the opportunities at Novo Nordisk? Or you have substantial clinical and research experience – ideally within diabetes and are looking for new challenges? Then, take a look at the opportunities within our Diabetes area! The positionWe are searching for new passionate...


  • Søborg, Denmark Novo Nordisk Full time

    The position is in DP MSAT department, Manufacturing Science and Technology, a team consisting of highly experienced specialists and professionals with strong knowledge and background in pharmaceutical sciences. You will become a part of an international, diverse and well-functioning team that enjoy solving problems in collaboration. Working at Novo...

  • Senior Manager

    3 weeks ago


    Søborg, Denmark Novo Nordisk Full time

    The position As Senior Manager your focus will be to lead a growing unit of professionals and specialists responsible for implementing new production at new or existing Contract Manufacturing Organisations (CMOs) within Drug Substance. Your main responsibilities include: Overseeing a team of currently six highly educated and dedicated professionals and...