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A 3-year PhD scholarship is available at the Center for Fast Ultrasound Imaging (CFU), Department of Electrical Engineering from January 2018 co-funded by the Innovation Foundation. The scholarship is in collaboration between CFU at DTU Elektro, DTU Nanotech, BK Medical, University of Copenhagen, and the Copenhagen University Hospital (Rigshospitalet).
The project seeks to develop new advanced ultrasound super resolution imaging (SRI) techniques. SRI can increase the fundamental resolution of ultrasound by a factor of 10-100 times using isolation and tracking of micro bubbles injected into the blood stream.
The projects develops the schemes for isolating the bubbles, for tracking and visualizing them in 2D and 3D. The project also includes performing a range of phantom and animal experiments to develop and refine the SRI algorithms.
Laerdal Copenhagen A/S, Copenhagen
The Laerdal Copenhagen office is our global headquarters for software research and development. More than half a million healthcare providers use our e-learning products each year, and we intend to expand to millions of users very soon.
You will have primary ownership of our self-directed e-learning software, which teaches people how to perform quality CPR using a manikin, voice feedback, and computer-based coaching.
You will be:
- Acting as the product owner on our Agile/Scrum Development Team, scoping, describing, and approving product enhancements in partnership with the team
- Ensuring that the team prioritizes those improvements and features that provide the most impact to our learners and customers
- Writing and reviewing product and program requirements based on input from the design team, our partners, our customers, and our end-users
Do you want to work for a Global Pharmaceutical company where you will be recognized for your contribution and commitment? Look no further, apply today for a position as Nordic Medical Advisor in Novartis. We are looking for someone with dedication and drive, who can take on our proud tradition within transplantation, and also bring value on other areas. A background within the field of transplant is a clear preference, alternatively solid experience within medical affairs.
- Medical Affairs Strategy and Operations
- Participates in the development of strategic plans in collaboration with other teams to drive the success of Novartis products
- Collaborates with Trial Monitoring Operations, advises / recommends potential investigators for local and global studies, ensuring the right mix of investigators
Do you want to work for a Global Pharmaceutical company where you will be recognized for your contribution and commitment? Look no further, apply today for Medical Affairs Training Manager in Nordics.
The primary responsibility of the Medical Affairs Training Manager is to create, implement and deliver a standardized approach for new hire training, continuous learning (including face-to-face field visits/meetings) for the medical organization with focus on field activities to secure optimal effectiveness and high quality performance.
- In collaboration with Franchise Medical Heads, CSO, Nordic Head of Commercial and Medical training and other relevant resources assist with needs analysis to determine knowledge, skills and behavior gaps for field medical associates.
- Actively contribute to development and continuous refinement of the Medical training curriculum.
Are you motivated by achieving results through and together with your team, and are you passionate about solving statistical challenges in a company striving for global leadership within psychiatry and neurology by improving the lives of patients; then you hold the right skills for our vacant position as Manager of Biostatistics in the Statistics Department at H. Lundbeck A/S in Copenhagen.
As a Manager in Biostatistics, you manage a team of approximately 10 Biostatisticians specialised in working with scientific and methodological aspects within the field of Clinical Research & Development. Your main responsibility is to lead, advice, coach and develop your employees and to employ new team members. At the same time you are responsible for planning and follow-up of activities and resources. You will report to the Snr Director of Statistics and be member of the Management Team.
LEO Pharma, Ballerup
Are YOU ready for a career change? Perhaps you are currently working as a nurse at a University Hospital involved in clinical trials or at a GP office and you would like to work in the Pharma Industry? Or you are working in Pharmacovigilance (e.g. as Drug Safety Associate) and would like to change into the clinical trial area?
As Clinical Data Manager you will be responsible for accurate, timely and consistent clinical data. You will provide clinical data management support to cross functional trial teams. You will have the opportunity to work with world-wide:
- Phase I trials: First-in-man trials
- Phase II trials: Dose-finding trials
Interacoustics A/S, Middelfart
Do you want to be part of something big and apply your theoretical knowledge and analytical skills whilst contributing to the work processes across the world in a truly global setting? Are you analytical, possess a winning personality, as well as passionate about both strategic and operational tasks? Then this is a unique chance for you to join a brand new Diagnostic Business Graduate Programme where you can become part of Diagnostic Instruments, a business area in William Demant - a leading, international OMX C25 company and a world leader within the hearing healthcare sector.
The Diagnostic Programme is a 2-year programme, during which you will explore the business area and develop your personal and professional skills through four job rotations of 6 months in various parts of the business here in Denmark or around the world.
Symphogen A/S, Ballerup
Symphogen is currently experiencing an increase in activities within both the early and late stage projects. Furthermore, Symphogen is planning to start phase III clinical trials and to apply for a Manufacturing and Import Authorization (§39 Licence).
Symphogen therefore plans to strengthen the QA organization with a Quality Manager.
As Quality Manager you will be involved in every step of the manufacturing process from generation of cell banks, upstream and downstream processes, final formulation, filling, analysis and release of the final drug product. The manufacturing is outsourced to various CMO's in EU and US.
The Quality Manager will participate for the quality group in our projects covering process and analytical validation, PPQ, clinical supply, and eventually marketing application.
Novo Nordisk A/S, Søborg
Are you motivated by setting up and driving global clinical programmes and do you want to exert your influence by leading project teams to develop haemophilia treatments? Do you thrive by working in an international environment and are you prepared to join an area with a high level of awareness and attention? Then we may have just the right job for you.
As a CPM, you are responsible for directing and co-driving one or more global clinical programme from an operational perspective. Currently, the department has several projects ranging from pre-clinical stages through marketed products. You will ensure that project key deliverables are met timely at a high quality and within budget by applying your project leadership as well as extensive operational Trial Management (TM) knowledge.
Novo Nordisk A/S, Bagsværd
Do you want to contribute to the safety and quality of Novo Nordisk clinical development? Do you have the competence and the medical knowledge it takes to handle adverse events reported from clinical trials? Would you enjoy being a key player in making sure that global regulatory requirements are met? Then you might be one of the Clinical Safety Associates we are looking for.
In order to ensure that global regulatory requirements are met, you will play a defining role in handling serious adverse events reported from our clinical trials. You will make sure that the individual adverse event reports are accurately and consistently registered and evaluated in our database and assess the need of requesting missing or follow up information on the reported events.
A combined position as professor with specific responsibilities in radiation therapy and as medical physicist is vacant at the Research Unit of Oncology, Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark and at the Department of Oncology, Odense University Hospital, respectively.
The position is for 5 years with the possibility of extension.
The posts are considered as one entity.
A combined position as clinical professor in radiation therapy and as consultant in clinical oncology is vacant at the Research Unit of Oncology, Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark and at the Department of Oncology, Odense University Hospital, respectively.
The position is for 5 years with the possibility of extension.
The posts are considered as one entity.
HERAX is looking for Consultants and Project Managers with experience from the pharmaceutical industry either from implementation of IT solutions or from working within the Life Sciences business area, or Life Science /IT graduates with preferably 1 – 2 years of experience.
As a Consultant/Project Manager, you will be part of or leading a small team of specialists, working closely with the clients in planning and executing process optimization- and IT projects within Research and Development. You will be involved in all project phases from the idea phase, to identifying the value adding areas, analyzing current and future processes and technology.
Radiometer Medical ApS, Brønshøj
If you are ready to set the direction for our Global Medical Affairs strategy for our many interesting and market-leading products and lead your own team of 4 Medical Advisors, then this could be your next career move.
- Lead and execute the Medical Affairs Strategy and operational plan to create value for key customers and the overall business
- Lead and develop the Medical Affairs team successfully included but not limited to performance management, talent management and training
- Accountable for understanding the external agenda
A 3-year PhD position is available at MagVenture A/S and DTU Electrical Engineering supported by the Industrial PhD program of the Innovation Fund Denmark.
It is a collaborative project led by Associate Professors Axel Thielscher (DTU) and Dr. Claus Mathiesen (MagVenture A/S). The successful candidate will be enrolled at the PhD school of DTU Electrical Engineering, and will be hosted at both MagVenture A/S and DTU.
Transcranial magnetic stimulation (TMS) is a non-invasive method to stimulate the brain, with several medical and research applications such as depression treatment.
As specialist in the Section of In Vitro studies you will join a group of one academic (Head of Section) and three experienced technicians to deliver in vitro toxicological support to early discovery projects. As an expert in in vitro methods and/or molecular toxicology we envisage that you will actively take part in developing and optimising our current high content screening methods and propose new in vitro and/or in silico screening strategies, when relevant.
A very exciting and dynamic research environment with experienced, collaborative colleagues. We are dedicated in our work and take pride in delivering high quality results and safety assessments that support research projects in the best possible way. The working atmosphere is informal and positive, offering good opportunities for collaboration and personal development.
Are you looking for high-level challenges within audiology research, enabling you to make a real difference in people’s lives? Can you imagine yourself in the unique challenge of being a leading person in an ambitious team that builds the evidence-base of Oticon Audiology and representing us at audiology events? Moreover, at the same time driving research you are passionate about?
In your new job, you will be part of the Centre for Applied Audiology Research, which consists of eight researchers and two student research assistants. We do research and communication related to hearing technology and hearing aid benefits. These benefits are documented through scientific publications, technical documentations provided by internal collaborators or through clinical research with independent research partners.
Unique Human Capital recruiting on behalf of Genmab in Copenhagen or Utrecht
Strong Project Manager to lead cross-functional early stage antibody product development
In order to strengthen the Project Management team, Genmab is looking for an experienced Compound Development Team Leader (CDTL) who will be based in Copenhagen or Utrecht.
As CDTL at Genmab, you will provide leadership to cross-functional international project teams. You will report to the Vice President, Project Management and to the Senior Director, Operations and Resource Management.
As CDTL you will :
- Develop and execute the project strategy for early stage antibody development projects from clinical candidate selection up to and including first human trials.
- Lead Compound Development Teams (CDTs) for two to three (co development) projects at different stages.
Compass Human Resources Group A/S recruiting on behalf of Sanofi in Hørsholm
As Medical Advisor for Sanofi, you will provide medical and scientific expertise and service for the diabetes and cardiovascular (DCV) team in Denmark. You will report directly to the DCV Medical Head Denmark and be a part of the Nordic & Baltic Medical Affairs organisation.
Sanofi has interesting products in the pipeline within both disease areas and you will be a crucial part in preparing the launches. This means that you will have an extrovert position having peer to peer discussions with key opinion leaders, discussing, developing and setting up relevant studies and data generation and projects as well as providing medical education internally in Sanofi and externally.
There could be several entries to this job, and your background could be one of the following: As a Medical Advisor, or another related experience as a Medical Doctor.
Novo Nordisk A/S, Bagsværd
Do you want to be part of a high performing team in one of the world’s leading pharmaceutical companies? Then you might be the right person for Novo Nordisk, as we are currently searching for an enthusiastic Corporate Counsel to be part of the Pharma Law team.
We offer an exciting and challenging position as Corporate Counsel, with a key focus on the following tasks: reviewing, drafting and negotiating complex contracts and related documentation, especially in in relation to outsourcing of clinical trials but also within other areas; maintaining and revising global corporate contract templates; participating in cross-functional working groups and providing legal advice to our key business stakeholders, primarily Global Development and Regulatory Affairs; preparing and providing training, guidelines and tools to our global legal and business stakeholders; driving ad hoc strategic projects.