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Unwire is currently looking for backend developers who wants to play a major role on the future of mobility. Would you like to join a highly experienced mobility team where you will have opportunities to develop technology platforms for transit agencies and operators – and at the same time contribute to a greener and more sustainable world? At Unwire we are passionate about our mobility platform and how we can help transit agencies make shared transportation more attractive. If you are equally as passionate as we are and if you would like to develop your knowledge and your skills together with us then please read on! You now have the possibility to be joining a team focusing on extending our Mobility as a Service capabilities. You will get the opportunity to learn about account-based ticketing, trip planning, ride booking, mobility services, payment processing, and much more. The position requires you to be inquisitive, to listen and learn, follow best practices, and deliver...

We are seeking an experienced automation test engineer to join our highly experienced mobility team where you will have opportunities to test great mobile platforms for transit agencies. We are passionate about our mobility platform and how we can help transit agencies make shared transportation more attractive. We are seeking someone who is equally as passionate and who would like to develop their knowledge and their skills together with us. We are a company where your opinion matters and where you can make an impact every day. The position requires you to be inquisitive, to listen and learn, follow best practices and deliver high quality code. You will be joining a team focusing on strengthening the REST API test automation for our Mobility as a Service micro-services running in AWS. You will work side-by-side with the backend development teams to develop the right automated testing strategy, select the right tools and ensure we hit the right coverage in all our build/ release...

Boligsocial medarbejder Info Jobbeskrivelse Boligsocial medarbejder Brænder du for at øge børn og unges fremtidsmuligheder? Kan du tilrettelægge og gennemføre aktiviteter, der styrker børns fællesskab og mod til at prøve kræfter med foreningslivet eller fritidsjob? Og kunne du tænke dig at arbejde med bydelsmødre? Så er det måske dig, vi mangler i vores boligsociale helhedsplan i Nivå og Kokkedal. Læs stillingsopslaget og søg her (du sendes videre til Jobindex)

Forstår du dig på myndighedsarbejde med socialt udsatte borgere og borgere med fysiske og/eller psykiske udfordringer? Er du motiveret for sammen med gode kollegaer at skabe løsninger på et højt fagligt niveau med fokus på borgernes egne ønske og drømme? - Så søg job hos os. Vi søger 2 fagligt dygtige kollegaer til myndighedsopgaver på det specialiserede socialområde efter Servicelovens voksenbestemmelser. Vi er 2 selvstændige myndighedsteams. Hvert team består af 4 sagsbehandlere og 1 faglig koordinator. Døgnteamet, hvor vi træffer afgørelser indenfor botilbudsområdet, herunder forsorgscenter og krisecenter samt Det Rehabiliterende team, hvor vi træffer afgørelser om socialpædagogisk støtte, dagtilbud m.m. For begge teams gælder, at der er tæt sparring om opgaverne, og begge teams har delvis egen kompetence. Vi arbejder på nuværende tidspunkt med VUM 1.0 med planlagt implementering af VUM 2.0 i efteråret 2023. Vi ønsker os 2 kollegaer, der har følgende faglige og personlige...

Er du sundhedsfagligt uddannet og ønsker du at arbejde med unge mennesker i alderen 18-35 år? Kan du inspirere og motivere, og har du solid erfaring med at arbejde med sundhed, motivation og samskabelse? Vil du være med til at sætte kursen for den rehabiliterende indsats på det socialpsykiatriske botilbud Thorupgården? Så er du måske vores nye kollega. Vi søger en ny kollega med sundhedsfaglig baggrund til Team Ung på vores fantastiske botilbud, som har en central placering i København. Botilbuddet Thorupgården er en del af Center for Unge og Midlertidige Botilbud. Vores mål er at fastholde og skabe en stærk ramme for sundhed, udvikling samt meningsfulde aktiviteter for mennesker med psykiatriske udfordringer. På Thorupgården er der i alt 112 boliger fordelt på §§ 107 og 108, hvoraf de 34 af dem er knyttet til Team Ung. Udover at du skal være med til at styrke det sundhedsfaglige arbejde på afdelingen, så forventer vi, at du som kontaktperson kan skabe en ramme for udvikling i...

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. The Role We are looking for an experienced and dedicated Associate Medical Director to be a part of our Global Clinical Development Team (Hematology). The Associate Medical Director will be accountable for the medical oversight of one or more clinical trials, medical review and communication of data, and medical input into regulatory documents and presentations. This is a full time position that can be located either in Princeton NJ or Copenhagen DK. Partial remote/partial onsite work. Responsibilities: Directing study design, protocol development and execution of clinical research for pivotal cancer studies. Contributing to the overall medical strategy of the assigned clinical development programs and product pipeline as well as giving in-depth medical advice on potential new projects (internal and external)....

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. The Role As Associate Director, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related activities in close cooperation with the Safety Physicians. This position has a global perspective, and you will interact with stakeholders ranging from regulatory authorities and DMCs as well as colleagues from other Genmab sites. As Associate Director, Global Drug Safety and Pharmacovigilance Scientist, you will be part of a highly skilled and international team. The position reports to the Project Safety Physician Lead. Responsibilities Perform safety review of Adverse Event reports for Genmab products Perform ongoing surveillance (including signal detection/evaluation) of safety data from Genmab clinical trials Be the safety contact for other departments and ensure...

In our line of work, life isn’t a given - it’s the ultimate goal. When life takes an unexpected turn, our technology and solutions enable caregivers to make informed diagnostic decisions to improve patient care. This is our shared purpose at Radiometer and what unites all +4000 of us - no matter our roles or where in the world we’re located. Creating impactful innovations like ours, doesn’t happen overnight - it requires uncompromising persistency, passion, and a desire to make a difference. Here, you can learn, grow, and chart an uncommonly diverse career. Radiometer is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges. The is known for its scientific curiosity and ability to understand different therapeutic areas as well as collaborating with a cross functional team. Radiometer has a diverse and...

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. The Role As Clinical Trial Manager (CTM) in Clinical Operations at Genmab, you will: Lead one or more trials ensuring that key project deliverables are met with the overall goal of developing new and innovative treatments for cancer. Lead the cross-functional trial-specific trial team, including the CROs, to deliver clinical trials within budget and timelines and according to quality standards defined by regulations, Genmab SOPs and ICH-GCP. In the Trial Management team in Clinical Operations, we are currently more than 60 highly motivated and experienced people located in Denmark, US, the Netherlands, and Japan. Working in Clinical Operations is exciting, intense, challenging, and fun at the same time. The dedication, collaborative and knock-your-socks-off spirit of our employees are what really shapes our team. From day one,...

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. About Us 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 that is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions and have a lot of fun and bring a ton of care in pursuing them. If this inspires you and feels like a fit, then we’d love to have you join us. The Role & Department As Sponsor Oversight Lead, you will be in the Clinical Operations Team and responsible for the...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. The Role: Medical Director Rheumatology within ICON - This is an exciting opportunity to work within a fast-paced environment within a...

Brænder du for at yde en omsorgsfuld pleje og være en del af et stærkt fællesskab? Så læs videre! Du er vigtig for os Fællesskabet er afgørende, når vi skal være der for andre mennesker, som har brug for vores støtte. Hos os bliver du mødt af kollegaer og en ledelse, som tror på dig, din faglighed og din dømmekraft. Vi er et hjem, hvor vi gør os umage for at skabe en aktiv hverdag med mening, og hvor livet leves – hele livet. Hver morgen begynder en ny dag. Det betyder nye muligheder og en ny tid. Tiden er vigtig, fordi det er den, som vi alle arbejder med at udfylde med godt samvær, tryghed, individuelle muligheder, praktisk assistance og gode oplevelser. Intet menneske går igennem livet uden at få brug for hjælp og støtte på et tidspunkt. At arbejde på Chr. Have indebærer mange muligheder, et stort ansvar og ikke mindst en glæde over at se mennesker trives og være trygge. Derfor tror vi også på, at din høje faglighed skinner igennem ved alt, hvad du foretager dig. Som person er du...

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. The Role We are looking for an experienced and dedicated (Associate) Medical Director to be a part of our Global Clinical Development Team (Hematology). AS (Associate) Medical Director will be accountable for the medical oversight of one or more clinical trials, medical review and communication of data, and medical input into regulatory documents and presentations. This is a full time position that can be located either in Utrecht, NL or Copenhagen DK. Responsibilities: Directing study design, protocol development and execution of clinical research for pivotal cancer studies. Contributing to the overall medical strategy of the assigned clinical development programs and product pipeline as well as giving in-depth medical advice on potential new projects (internal and external). Generating/reviewing clinical components of key...

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. The Role We are looking for an experienced and dedicated Senior Clinical Trial Associate (CTA) to be part of Global Clinical Operations at our Headquarters in Copenhagen. Global Clinical Operations is part of Genmab Clinical Development and is responsible for managing the Genmab clinical cancer trials from early phase trials (FIH) to late stage trials while ensuring processes lives up to regulations and business ethics. The work environment is within a global setting and characterized by people empowerment, new challenges, and devoted and talented colleagues. In this position, you will be responsible for providing assistance to the Clinical Trial Manager on a number of clinical trials in all relevant aspects of trial preparation, trial conduct, documentation, and archiving. Responsibilities Responsible for setting-up,...

Genmab is focused on the creation and development of innovative and differentiated antibody products, with the aim of improving the lives of cancer patients. The Role Are you looking for an opportunity where you can take the lead in delivering key trial management elements on oncology trials and ensure sponsor engagement? We are looking for a (Senior) Clinical Trial Manager, someone driven by ensuring a one-team culture with CROs, and who excels in contributing to great teamwork and working environment. Join our innovative, hardworking, and ambitious team collaborating in a high-performing and fast-paced environment dedicated to improving the lives of cancer patients. As (Senior) Clinical Trial Manager (CTM) in Clinical Operations at Genmab, you will: Lead one or more trials ensuring that key project deliverables are met with the overall goal of developing new and innovative treatments for cancer. Lead the cross-functional trial-specific trial team, including the CROs, to deliver...

? Social- og sundhedsassistent med initiativ og overblik til dagvagt i et moderne plejecenter Vi søger en engageret, fagligt dygtig og god kollega på 30-37 timer ugentligt. ?Vi har fokus på, at beboerne får den bedste pleje og omsorg afhængig af deres behov. Vi arbejder med kvalitetsudvikling og patientsikkerhed, for at sikre høj faglig kvalitet i omsorg og sygepleje I plejecentret arbejder vi tæt sammen. Vi er opdelte i mindre teams, vi hjælper hinanden, er flexible og løser hverdagens opgaver i et tværfagligt samarbejde. ?Der vil være weekendvagt hver 3. weekend og indimellem som ansvarshavende social- og sundhedsassistent. Du skal som social- og sundhedsassistent være en god rollemodel i gruppen, og du vil have gode muligheder for at være sparringspartner med sygeplejersken. Vi forventer, at du: Er uddannet og autoriseret som Social- og Sundhedsassistent Med din faglighed sikrer et fagligt velfunderet fokus på kerneopgaven og har en bred erfaring med løsning af mange forskellige...

Gamucatex Copenhagen Student Internship Salary Unpaid Do you want to be part of developing an innovative and meaningful game? Are you interested in user-centered and user-driven design? And are you eager to apply your qualitative and quantitative research methods to understand the wants, needs, and pain-points of users to create the best user experience possible? If you’re nodding “YES” to the above, then we are interested in you as well as we are looking for a highly motivated and skilled individual to plan and conduct user related research within our organization. About our game We are developing a digital autobattler card based game in a historical and mythological universe. The aim is to make a historically accurate game that inspires people to immerse themselves into history. The upcoming game is in production check it out at our itch.io: https://gamucatex.itch.io/tectonicus The player will be taking charge of a faction, either Viking, Frankian or English which they will follow...

Skanderborg og Aarhus kommune Til en igangværende indsats, søger vi en eller flere, erfarne, empatiske og dedikerede SSA eller SSH medarbejdere. Indsatsen indebærer interessante opgaver indenfor psykiatri og demensområdet, til allerede faste projekter, hvor du vil skulle arbejde i et mindre og fast team. Herudover forudsætter indsatsen at du er kan se dig selv, som en rolig og faglig bevidst nøgleperson, evt. med mulighed for at blive fast tovholder på indsatsen, i samarbejde med vores faglige leder. Vi tilbyder ordnede arbejdsforhold, i en virksomhed, hvor vi arbejder nærværende, og borgerperspektiveret. Stillingen består af vagter á 12 timers varighed, fordelt på ugens 7 dage, både dag og aften. Timeantal efter aftale – der er dog også mulighed for at få fuldtid (37 timer) på denne indsats. K rav til ansøger: Du er faglært SSA eller SSH Du har min. 2 års praksiserfaring fra socialområdet Evner at stå i konfliktsituationer og har erfaring med konflikthåndtering og udadrettet adfærd...

The Role: Medical Director Rheumatology within ICON - This is an exciting opportunity to work within a fast-paced environment within a culture derived from collaboration, partnership and accountability. ICON is a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Responsibilities include: Providing medical leadership on project teams Providing medical I scientific consultation and therapeutic expertise Overseeing study specific medical/safety monitoring activities, ensuring compliance with ethical, legal, and regulatory standards as well as ICON and Sponsor SOPs Representing the Medical Affairs Department in business development activities Providing functional/departmental oversight in the absence of Senior Medical Director I Vice President, Medical Affairs Requirements for the role include: 5 plus years' experience in Rheumatology and a board certification in Rheumatology 2-3 plus years' experience in...