Statisticians on different seniority levels for Clinical Development in Søborg and Aalborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, have a huge variety of tasks and great opportunities to learn and engage in a strong scientific community? Then you may be one of our Statisticians. We are looking to employ a number of biostatisticians at all seniority levels.

In Global Development, we take responsibility for new products based on proteins and peptides from early development phases to product launch and life cycle management. We are responsible for managing clinical drug development worldwide, securing that the process lives up to uniform global standards, regulations and business ethics. We work in global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society.

About the department

The Biostatistics function currently consists of approximately 250 statisticians and statistical programmers globally. Of these, 170 are situated in Denmark, where we are organised in departments supporting our development projects (e.g. GLP-1, Insulin, Haemophilia or Obesity). Novo Nordisk has a broad R&D pipeline and majority of our statistical work is done in-house, thus we offer a wide variety of statistical challenges and provide a strong scientific community. We are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders.

 

Biostatistics is a very dynamic area which cooperates with many different professionals in the organisation both within Denmark and across borders with our colleagues in India, China and Japan as well as our outsourcing partners in India and Europe. Thus, we have an international and challenging environment where you can use your cross cultural awareness and managerial skills.


You will be working out of our office buildings in either Søborg or Aalborg. Please state in your application if you prefer to be based in Søborg or Aalborg.

The positions
As we are looking for a number of new biostatisticians, the jobs vary in content and responsibility.

As a Statistician you are responsible for planning, coordinating and executing clinical trials and other tasks within clinical development. As Statistician you will be responsible for giving input to protocols and statistical analyses, analysing and interpreting trial results and handle day-to-day statistical issues during the course of the trial. Other activities include input to manuscripts, posters, risk management plans and other safety reports. Furthermore, you will be engaged in coordinating and supervising the work of contract houses around the world performing outsourced statistical tasks.

As Statistics Specialist you are responsible for planning and coordinating both standard and more complex and time critical statistical tasks. You are responsible for providing statistical input to project development plans, trial designs, clinical trial protocols, summary documents and publications. You will be involved in presentation and discussion of results both internally and externally and participate in meetings with regulatory authorities and external collaborators. You handle many assignments concurrently and will work in close collaboration with a team of Statisticians and Statistical Programmers.

Regardless your seniority, you will collaborate closely with other Statisticians, Statistical Programmers and interact in our cross-disciplinary teams. You will interact in cross-disciplinary development teams across country borders and communicate statistical issues and ideas to non-statisticians. Dependent on your qualifications, you may be involved in coaching of less experienced colleagues and be responsible for coordinating and supervising the work of contract houses around the world performing outsourced tasks. Therefore, we expect you to be able to communicate statistical problems and ideas clearly.

Development of methods and processes as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in our dedicated efforts to make Biostatistics a good and challenging place to work. In exchange we offer great opportunities for ongoing training to ensure your continued competency development.

Qualifications
You have a solid theoretical background in statistics corresponding to M.Sc. level, and you bring in depth understanding of practical statistical problems. If you additionally bring statistical experience within the pharmaceutical industry and/or SAS experience it will be an advantage but not a prerequisite. In addition, candidates for Statistics Specialist level positions will have at least eight years of experience within clinical or bio-statistical research and ability to act as driver and leading member of the project teams you are part of, and if you have experience from project management and supervision of colleagues, it will be an advantage.

Since you will be participating in cross-disciplinary development teams across country borders we expect you to have the ability to communicate statistical issues and ideas to non-statisticians. That is why good communication skills and fluency in English is required.

Working at Novo Nordisk
By being patient-focused, we have achieved a market leading position and we continuously develop our expertise to stay ahead – both as a company and as individuals. Working here mean joining a team of highly qualified, ambitious colleagues with a passion to bring better treatments to the people who need them. We strive for always keeping our positive and collaborative atmosphere in our daily work and there is good work-life-balance.

Contact
For further information, please contact Peter F. Christens at +45 3079 9440 or Christian Løve at +45 3077 7626.

Deadline
All enquiries will be handled confidentially. Please submit your cover letter (application), CV and other relevant papers online no later than October 25, 2019. We are screening and interviewing on an ongoing basis so please do not hesitate to apply.

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


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330091500Phoenix-1989905a12019-10-07T00:00:00Statisticians on different seniority levels for Clinical Development in Søborg and Aalborg

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, have a huge variety of tasks and great opportunities to learn and engage in a strong scientific community? Then you may be one of our Statisticians. We are looking to employ a number of biostatisticians at all seniority levels.

In Global Development, we take responsibility for new products based on proteins and peptides from early development phases to product launch and life cycle management. We are responsible for managing clinical drug development worldwide, securing that the process lives up to uniform global standards, regulations and business ethics. We work in global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society.

About the department

The Biostatistics function currently consists of approximately 250 statisticians and statistical programmers globally. Of these, 170 are situated in Denmark, where we are organised in departments supporting our development projects (e.g. GLP-1, Insulin, Haemophilia or Obesity). Novo Nordisk has a broad R&D pipeline and majority of our statistical work is done in-house, thus we offer a wide variety of statistical challenges and provide a strong scientific community. We are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders.

 

Biostatistics is a very dynamic area which cooperates with many different professionals in the organisation both within Denmark and across borders with our colleagues in India, China and Japan as well as our outsourcing partners in India and Europe. Thus, we have an international and challenging environment where you can use your cross cultural awareness and managerial skills.


You will be working out of our office buildings in either Søborg or Aalborg. Please state in your application if you prefer to be based in Søborg or Aalborg.

The positions
As we are looking for a number of new biostatisticians, the jobs vary in content and responsibility.

As a Statistician you are responsible for planning, coordinating and executing clinical trials and other tasks within clinical development. As Statistician you will be responsible for giving input to protocols and statistical analyses, analysing and interpreting trial results and handle day-to-day statistical issues during the course of the trial. Other activities include input to manuscripts, posters, risk management plans and other safety reports. Furthermore, you will be engaged in coordinating and supervising the work of contract houses around the world performing outsourced statistical tasks.

As Statistics Specialist you are responsible for planning and coordinating both standard and more complex and time critical statistical tasks. You are responsible for providing statistical input to project development plans, trial designs, clinical trial protocols, summary documents and publications. You will be involved in presentation and discussion of results both internally and externally and participate in meetings with regulatory authorities and external collaborators. You handle many assignments concurrently and will work in close collaboration with a team of Statisticians and Statistical Programmers.

Regardless your seniority, you will collaborate closely with other Statisticians, Statistical Programmers and interact in our cross-disciplinary teams. You will interact in cross-disciplinary development teams across country borders and communicate statistical issues and ideas to non-statisticians. Dependent on your qualifications, you may be involved in coaching of less experienced colleagues and be responsible for coordinating and supervising the work of contract houses around the world performing outsourced tasks. Therefore, we expect you to be able to communicate statistical problems and ideas clearly.

Development of methods and processes as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in our dedicated efforts to make Biostatistics a good and challenging place to work. In exchange we offer great opportunities for ongoing training to ensure your continued competency development.

Qualifications
You have a solid theoretical background in statistics corresponding to M.Sc. level, and you bring in depth understanding of practical statistical problems. If you additionally bring statistical experience within the pharmaceutical industry and/or SAS experience it will be an advantage but not a prerequisite. In addition, candidates for Statistics Specialist level positions will have at least eight years of experience within clinical or bio-statistical research and ability to act as driver and leading member of the project teams you are part of, and if you have experience from project management and supervision of colleagues, it will be an advantage.

Since you will be participating in cross-disciplinary development teams across country borders we expect you to have the ability to communicate statistical issues and ideas to non-statisticians. That is why good communication skills and fluency in English is required.

Working at Novo Nordisk
By being patient-focused, we have achieved a market leading position and we continuously develop our expertise to stay ahead – both as a company and as individuals. Working here mean joining a team of highly qualified, ambitious colleagues with a passion to bring better treatments to the people who need them. We strive for always keeping our positive and collaborative atmosphere in our daily work and there is good work-life-balance.

Contact
For further information, please contact Peter F. Christens at +45 3079 9440 or Christian Løve at +45 3077 7626.

Deadline
All enquiries will be handled confidentially. Please submit your cover letter (application), CV and other relevant papers online no later than October 25, 2019. We are screening and interviewing on an ongoing basis so please do not hesitate to apply.

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

Are you interested in working with biological data and would you like to be part of a future with a strong pipeline of products, have a huge variety of tasks and great opportunities to learn and engage in a strong scientific community? Then you may be one of our Statisticians. We are looking to employ a number of biostatisticians at all seniority levels. In Global Development, we take responsibility for new products based on proteins and peptides from early development phases to product launch and life cycle management. We are responsible for managing clinical drug development worldwide, securing that the process lives up to uniform global standards, regulations and business ethics. We work in global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society. About the department The Biostatistics function currently consists of approximately 250 statisticians and statistical programmers globally. Of these, 170 are situated in Denmark, where we are organised in departments supporting our development projects (e.g. GLP-1, Insulin, Haemophilia or Obesity). Novo Nordisk has a broad R D pipeline and majority of our statistical work is done in-house, thus we offer a wide variety of statistical challenges and provide a strong scientific community. We are organised in smaller units for each clinical project to ensure close collaboration with our various stakeholders. Biostatistics is a very dynamic area which cooperates with many different professionals in the organisation both within Denmark and across borders with our colleagues in India, China and Japan as well as our outsourcing partners in India and Europe. Thus, we have an international and challenging environment where you can use your cross cultural awareness and managerial skills. You will be working out of our office buildings in either Søborg or Aalborg. Please state in your application if you prefer to be based in Søborg or Aalborg. The positions As we are looking for a number of new biostatisticians, the jobs vary in content and responsibility. As a Statistician you are responsible for planning, coordinating and executing clinical trials and other tasks within clinical development. As Statistician you will be responsible for giving input to protocols and statistical analyses, analysing and interpreting trial results and handle day-to-day statistical issues during the course of the trial. Other activities include input to manuscripts, posters, risk management plans and other safety reports. Furthermore, you will be engaged in coordinating and supervising the work of contract houses around the world performing outsourced statistical tasks. As Statistics Specialist you are responsible for planning and coordinating both standard and more complex and time critical statistical tasks. You are responsible for providing statistical input to project development plans, trial designs, clinical trial protocols, summary documents and publications. You will be involved in presentation and discussion of results both internally and externally and participate in meetings with regulatory authorities and external collaborators. You handle many assignments concurrently and will work in close collaboration with a team of Statisticians and Statistical Programmers. Regardless your seniority, you will collaborate closely with other Statisticians, Statistical Programmers and interact in our cross-disciplinary teams. You will interact in cross-disciplinary development teams across country borders and communicate statistical issues and ideas to non-statisticians. Dependent on your qualifications, you may be involved in coaching of less experienced colleagues and be responsible for coordinating and supervising the work of contract houses around the world performing outsourced tasks. Therefore, we expect you to be able to communicate statistical problems and ideas clearly. Development of methods and processes as well as knowledge sharing is continuously on-going in Novo Nordisk, especially based on the initiative of the employees. We expect you to take part in our dedicated efforts to make Biostatistics a good and challenging place to work. In exchange we offer great opportunities for ongoing training to ensure your continued competency development. Qualifications You have a solid theoretical background in statistics corresponding to M.Sc. level, and you bring in depth understanding of practical statistical problems. If you additionally bring statistical experience within the pharmaceutical industry and or SAS experience it will be an advantage but not a prerequisite. In addition, candidates for Statistics Specialist level positions will have at least eight years of experience within clinical or bio-statistical research and ability to act as driver and leading member of the project teams you are part of, and if you have experience from project management and supervision of colleagues, it will be an advantage. Since you will be participating in cross-disciplinary development teams across country borders we expect you to have the ability to communicate statistical issues and ideas to non-statisticians. That is why good communication skills and fluency in English is required. Working at Novo Nordisk By being patient-focused, we have achieved a market leading position and we continuously develop our expertise to stay ahead both as a company and as individuals. Working here mean joining a team of highly qualified, ambitious colleagues with a passion to bring better treatments to the people who need them. We strive for always keeping our positive and collaborative atmosphere in our daily work and there is good work-life-balance. Contact For further information, please contact Peter F. Christens at 45 3079 9440 or Christian Løve at 45 3077 7626. Deadline All enquiries will be handled confidentially. Please submit your cover letter (application), CV and other relevant papers online no later than October 25, 2019. We are screening and interviewing on an ongoing basis so please do not hesitate to apply. Millions rely on us To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.11jobnet1989905a100000000000aDK_OFIR_02DKDanmark228DKK2019-10-25T00:00:000000https://www.novonordisk.com/careers/working-at-novo-nordisk/job-ad-display.14792.en_GB.html0EuropaDanmarkSjælland & øerStorkøbenhavnKøbenhavnEuropaDanmarkSjælland & øerStorkøbenhavnGentofteEuropaDanmarkSjælland & øerStorkøbenhavnGladsaxe3613818Novo Nordisk A/S11Vandtårnsvej 1082860SøborgDKDanmark0DKDanmarkDKDanmark8Fuldtid46Permanent825213JobNet5046055504605510017-09-20190https://dispatcher.ofir.dk/statistic/register?context=FeedEntrySearchedCount&feedId=dc2beb84&entryId=1989905ahttps://dispatcher.ofir.dk/statistic/register?context=FeedEntryDisplayCount&feedId=dc2beb84&entryId=1989905ahttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationInitiatedCount&feedId=dc2beb84&entryId=1989905a&page=ShowJob&component=SendApplicationButtonhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationAppliedCount&feedId=dc2beb84&entryId=1989905a&page=EmailApplyForm&component=SendApplicationButtonhttps://static.matchwork.com/company/logo/DK/ORS/SoMe/Finans_og_oekonomi/Oekonomi/3.jpgStatisticians on different seniority levels for Clinical Development in Søborg and Aalborg12008001Dansk3Læse/ tale212201Statistiker3Økonomi362747965noreply@ofir.comDKDanmarkDKDanmark330107687StatisticianRobot Manufacturing Bagsværd Do you want to support the production of insulin in Novo Nordisk? Are you eager to develop data-based solutions, spread the use of statistical methods and work with optimisation and improvement projects within Diabetes Finished Products (DFP)? If so, we offer a challenging position as statistician in DFP Improvement Projects Data Science. About the department Site Support Improvements supports our global DFP production sites in manufacturing diabetes products, and sets the direction for new technology, innovation and production optimization. A high level of knowledge and process understanding is anchored in the department. As a statistician you will be working in a team consisting of 6 project managers and 5 statisticians. We are an ambitious and high performing team known for delivering strong results that add to the success of Novo Nordisk. We value creativity and innovation and the ability to work with people with different backgrounds. We share a relaxed tone and high ambitions. The job Your main task as a statistician will be to provide statistical support to Process Experts, Project Managers and other customers based on deep involvement in the actual assignment. You will be working in close cooperation with colleagues of other areas of expertise, focusing on understanding their problems, sparring during development of statistical solutions and communicating the solutions. Furthermore, you will drive or participate in optimisation and improvements projects to enhance the use of statistical methods. The statistical tools are mainly Design of Experiments, Mixed Models, Statistical Process Control, Acceptance Sampling, Generalised Linear Models and General Explorative Statistics. Qualifications You are a statistician with experience in applied statistics with a strong background in mathematical statistics as M.Sc. or Ph.D. in Statistics, Engineering or Mathematics. You can keep focus in complicated matters and handle many different tasks at the same time. You work independently with impact and high engagement. You have excellent communication and interpersonal skills. You speak and write English fluently. Experience with SAS for Windows and JMP is an advantage but not a requirement. Working at Novo Nordisk At Novo Nordisk we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth. Contact For further information please contact Mats Rasmussen at 45 30 75 36 08. Deadline: October 31, 2019 Millions rely on us To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
  • Manufacturing
  • Bagsværd

Do you want to support the production of insulin in Novo Nordisk? Are you eager to develop data-based solutions, spread the use of statistical methods and work with optimisation and improvement projects within Diabetes Finished Products (DFP)?

If so, we offer a challenging position as statistician in DFP Improvement Projects & Data Science.

About the department

Site Support & Improvements supports our global DFP production sites in manufacturing diabetes products, and sets the direction for new technology, innovation and production optimization. A high level of knowledge and process understanding is anchored in the department.

As a statistician you will be working in a team consisting of 6 project managers and 5 statisticians. We are an ambitious and high performing team known for delivering strong results that add to the success of Novo Nordisk. We value creativity and innovation and the ability to work with people with different backgrounds. We share a relaxed tone and high ambitions.


The job

Your main task as a statistician will be to provide statistical support to Process Experts, Project Managers and other customers based on deep involvement in the actual assignment.

You will be working in close cooperation with colleagues of other areas of expertise, focusing on understanding their problems, sparring during development of statistical solutions and communicating the solutions. Furthermore, you will drive or participate in optimisation and improvements projects to enhance the use of statistical methods.

The statistical tools are mainly Design of Experiments, Mixed Models, Statistical Process Control, Acceptance Sampling, Generalised Linear Models and General Explorative Statistics.

Qualifications

You are a statistician with experience in applied statistics with a strong background in mathematical statistics as M.Sc. or Ph.D. in Statistics, Engineering or Mathematics.

You can keep focus in complicated matters and handle many different tasks at the same time. You work independently with impact and high engagement. You have excellent communication and interpersonal skills. You speak and write English fluently.  Experience with SAS for Windows and JMP is an advantage but not a requirement.

Working at Novo Nordisk

At Novo Nordisk we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

 
Contact

For further information please contact Mats Rasmussen at +45 30 75 36 08.

Deadline: October 31, 2019

Millions rely on us

To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
 

NOVO NORDISK A/SBagsværd2019-10-15T00:00:002019-10-31T00:00:00
330106109RKKP søger datamanager med SAS-erfaring til Aarhus, Odense eller KøbenhavnRobot Regionernes Kliniske Kvalitetsudviklingsprogram (RKKP) søger en datamanager med SAS-erfaring, der brænder for at bidrage til at øge kvaliteten af patientbehandlingen ved hjælp af dataunderstøttet kvalitetsudvikling i sundhedsvæsenet Vil du være motiveret af at medvirke til at skabe viden til et bedre sundhedsvæsen og forbedre befolkningens sundhed og livskvalitet gennem datastøttet udvikling af sundhedsvæsenet? Har du lyst til at arbejde med datamanagement og analyse af forskellige typer af sundhedsdata og programmering af nationalt vedtagne indikatorer til monitorering af behandlingskvaliteten? Så er du måske vores nye kollega på en af RKKP s adresser i Odense, Århus eller København. Afdeling for databaseområde 1: Hjerte kar, kirurgi og akutområdet søger en datamanager pr. 1 1-2020 eller snarest muligt. Om RKKP Vi stræber efter høj og ensartet kvalitet i sundhedsvæsenet til gavn for borgere og patienter i Danmark. Vi understøtter, at der skabes enighed om, hvad der er & 39 god behandling& 39 , vi analyserer data og producerer viden i tæt samarbejde med klinikere, patienter og ledelser. Det gør vi ved at levere viden og bidrag til læring og forbedring i sundhedsvæsenet. RKKP er en netværksorganisation, bygget op omkring ca. 85 kliniske kvalitetsdatabaser, de tilhørende klinisk forankrede styregrupper og RKKP& 39 s Videncenter. Videncentret varetager bl.a. support af kliniske kvalitetsdatabaser i relation til epidemiologi, datamanagement biostatistik, it-drift og udvikling samt koordination og kommunikation. De kliniske kvalitetsdatabaser er baseret dels på data fra dedikerede indberetningssystemer, dels - og i stigende grad - på data fra nationale sundhedsregistre som fx Landspatientregistret (LPR) og de regionale elektroniske patientjournaler. Vi tilbyder en dynamisk organisation i rivende udvikling med strategiske målområder for 2019-2022en god blanding af drifts- og udviklingsopgaver, hvor vi hele tiden stræber efter at blive bedre tværfagligt samarbejde i teamstrukturer som bærende element i løsningen af opgaverne høj faglighed og stærk kollegial støtte og sparringgod mulighed for selv at præge den daglige arbejdstilrettelæggelseen uhøjtidelig omgangstone Dine opgaver Stillingen som datamanager er afvekslende, og der er gode faglige udviklingsmuligheder inden for vores opgaveportefølje. Du vil indgå i teams sammen med epidemiologer og kontaktpersoner omkring flere af de landsdækkende kliniske kvalitetsdatabaser. Teamet omkring den enkelte database skal ved fælles hjælp og samarbejde varetage indhentning, analyse og afrapportering af data til belysning af udviklingen af behandlingskvaliteten i hele landet og på de behandlende afdelinger. Dine opgaver vil blandt andet være:Databehandling af kildedata med henblik på opsætning og vedligehold af indikatoralgoritmer og patientpopulationer i SAS datavarehus, herunder medvirken til databasernes opstilling til LPR3Udarbejdelse af analyser og resultater til kvalitetsdatabasernes årsrapporterLevering data og resultater fra de kliniske kvalitetsdatabaser til de regionale ledelsesinformationssystemerUdtræk af data til forskningsbrugMødedeltagelse og sparring med databasernes kliniske styregrupperDeltagelse i videreudvikling af fælles metoder, programmer, dataskabeloner og hjælpeværktøjer. Din profil Vi lægger vægt på, at du:har praktisk erfaring med datamanagementhar erfaring med håndtering og analyse af sundhedsdata (herunder fx data fra Landspatientregistret)gerne har erfaring med statistiske analyser, fx Statistisk Proces Kontrolgerne har kendskab til SAS Data Integration Studiohar en relevant akademisk uddannelse, eksempelvis inden for matematik, statistik, bioinformatik, samfundsvidenskab, sundhedsteknologi (el.lign.).Du kan også være nyuddannet. Som person er det vigtigt, at du:er selvstændig, ansvarsfuld og grundig i dit arbejdeer en teamplayer, der som en naturlig del gerne giver en ekstra hånd med, når det brænder påvil trives med og ser en værdi i at arbejde ud fra fælles retningslinjer og metoder er analytisk og god til at dykke ned i detaljen og samtidig bevare overblikket kan indgå i dialog med forskellige faggrupper, både internt og eksternt Løn og ansættelsesforhold Stillingen er som udgangspunkt med en arbejdstid på 37 timer pr. uge. Løn- og ansættelsesvilkår er med udgangspunkt i gældende overenskomst med mulighed for forhandling af kvalifikations- og funktionstillæg. Arbejdssted bliver på en af vores adresser på Odense Universitetshospital, i Regionshuset i Aarhus eller København (Frederiksberg Hospital). Du kan forvente nogen rejseaktivitet i forbindelse med møder i databaserne og kontakt til øvrige kolleger på RKKP-adresserne. Ansøgningsfrist Send os din ansøgning, CV og uddannelsesbevis via vores online system senest søndag den 27. oktober 2019. Vi forventer at afholde ansættelsessamtaler i Odense den 1. november 2019. Hvis du har lyst til at høre nærmere om stillingen, er du velkommen til at kontakte afdelingsleder i afdeling for databaseområde 1, Charlotte Cerqueira på telefon 2921 4916. Du kan læse mere om RKKP på http: www.rkkp.dk om-rkkp Samvirker ? troværdighed ? engagement ? meningsfuldhed Da Region Midtjylland løbende gennemfører besparelser og omorganiseringer, vil medarbejdere i omplacering, der søger stillingen, have fortrinsret til samtale.Regionernes Kliniske Kvalitetsudviklingsprogram (RKKP) søger en datamanager med SAS-erfaring, der brænder for at bidrage til at øge kvaliteten af patientbehandlingen ved hjælp af dataunderstøttet kvalitetsudvikling i sundhedsvæsenet 
 
Vil du være motiveret af at medvirke til at skabe viden til et bedre sundhedsvæsen og forbedre befolkningens sundhed og livskvalitet gennem datastøttet udvikling af sundhedsvæsenet? Har du lyst til at arbejde med datamanagement og analyse af forskellige typer af sundhedsdata og programmering af nationalt vedtagne indikatorer til monitorering af behandlingskvaliteten? Så er du måske vores nye kollega på en af RKKP’s adresser i Odense, Århus eller København.

Afdeling for databaseområde 1: Hjerte/kar, kirurgi og akutområdet søger en datamanager pr. 1/1-2020 eller snarest muligt.
 
Om RKKP
Vi stræber efter høj og ensartet kvalitet i sundhedsvæsenet – til gavn for borgere og patienter i Danmark. Vi understøtter, at der skabes enighed om, hvad der er 'god behandling', vi analyserer data og producerer viden i tæt samarbejde med klinikere, patienter og ledelser. Det gør vi ved at levere viden og bidrag til læring og forbedring i sundhedsvæsenet. 

RKKP er en netværksorganisation, bygget op omkring ca. 85 kliniske kvalitetsdatabaser, de tilhørende klinisk forankrede styregrupper og RKKP's Videncenter. Videncentret varetager bl.a. support af kliniske kvalitetsdatabaser i relation til epidemiologi, datamanagement/biostatistik, it-drift og udvikling samt koordination og kommunikation. 

De kliniske kvalitetsdatabaser er baseret dels på data fra dedikerede indberetningssystemer, dels - og i stigende grad - på data fra nationale sundhedsregistre som fx Landspatientregistret (LPR) og de regionale elektroniske patientjournaler. 

Vi tilbyder 
  • en dynamisk organisation i rivende udvikling med strategiske målområder for 2019-2022
  • en god blanding af drifts- og udviklingsopgaver, hvor vi hele tiden stræber efter at blive bedre 
  • tværfagligt samarbejde i teamstrukturer som bærende element i løsningen af opgaverne 
  • høj faglighed og stærk kollegial støtte og sparring
  • god mulighed for selv at præge den daglige arbejdstilrettelæggelse
  • en uhøjtidelig omgangstone

Dine opgaver
Stillingen som datamanager er afvekslende, og der er gode faglige udviklingsmuligheder inden for vores opgaveportefølje. 
Du vil indgå i teams sammen med epidemiologer og kontaktpersoner omkring flere af de landsdækkende kliniske kvalitetsdatabaser.  Teamet omkring den enkelte database skal ved fælles hjælp og samarbejde varetage indhentning, analyse og afrapportering af data til belysning af udviklingen af behandlingskvaliteten i hele landet og på de behandlende afdelinger.  

Dine opgaver vil blandt andet være:
  • Databehandling af kildedata med henblik på opsætning og vedligehold af indikatoralgoritmer og patientpopulationer i SAS datavarehus, herunder medvirken til databasernes opstilling til LPR3
  • Udarbejdelse af analyser og resultater til kvalitetsdatabasernes årsrapporter
  • Levering data og resultater fra de kliniske kvalitetsdatabaser til de regionale ledelsesinformationssystemer
  • Udtræk af data til forskningsbrug
  • Mødedeltagelse og sparring med databasernes kliniske styregrupper
  • Deltagelse i videreudvikling af fælles metoder, programmer, dataskabeloner og hjælpeværktøjer. 

Din profil
Vi lægger vægt på, at du:
  • har praktisk erfaring med datamanagement
  • har erfaring med håndtering og analyse af sundhedsdata (herunder fx data fra Landspatientregistret)
  • gerne har erfaring med statistiske analyser, fx Statistisk Proces Kontrol
  • gerne har kendskab til SAS Data Integration Studio
  • har en relevant akademisk uddannelse, eksempelvis inden for matematik, statistik, bioinformatik, samfundsvidenskab, sundhedsteknologi (el.lign.).
Du kan også være nyuddannet.

Som person er det vigtigt, at du:
  • er selvstændig, ansvarsfuld og grundig i dit arbejde
  • er en teamplayer, der som en naturlig del gerne giver en ekstra hånd med, når det brænder på
  • vil trives med og ser en værdi i at arbejde ud fra fælles retningslinjer og metoder 
  • er analytisk og god til at dykke ned i detaljen og samtidig bevare overblikket 
  • kan indgå i dialog med forskellige faggrupper, både internt og eksternt

Løn og ansættelsesforhold
Stillingen er som udgangspunkt med en arbejdstid på 37 timer pr. uge. 
Løn- og ansættelsesvilkår er med udgangspunkt i gældende overenskomst med mulighed for forhandling af kvalifikations- og funktionstillæg.
Arbejdssted bliver på en af vores adresser på Odense Universitetshospital, i Regionshuset i Aarhus eller København (Frederiksberg Hospital).

Du kan forvente nogen rejseaktivitet i forbindelse med møder i databaserne og kontakt til øvrige kolleger på RKKP-adresserne.

Ansøgningsfrist
Send os din ansøgning, CV og uddannelsesbevis via vores online system senest søndag den 27. oktober 2019. 
Vi forventer at afholde ansættelsessamtaler i Odense den 1. november 2019.
 
Hvis du har lyst til at høre nærmere om stillingen, er du velkommen til at kontakte afdelingsleder i afdeling for databaseområde 1, Charlotte Cerqueira på telefon 2921 4916.
 
Du kan læse mere om RKKP på http://www.rkkp.dk/om-rkkp/ 

Samvirker ? troværdighed ? engagement ? meningsfuldhed



Da Region Midtjylland løbende gennemfører besparelser og omorganiseringer, vil medarbejdere i omplacering, der søger stillingen, have fortrinsret til samtale.


 

Region MidtjyllandFrederiksberg2019-10-11T00:00:002019-10-27T00:00:00
330095932Data Scientist for Text-Analytics Product DevelopmentRobot Summary FLINT Systems is a data analytics technology firm whose mission is to develop technologies based in computational linguistics to automatically process textual data for the purposes of authorship analysis. FLINT is a new technology start up that will focus its efforts upon the development of innovative technologies that will be used for purpose of forensic linguistic analysis. FLINT Forensic Linguistic software will be SaaS based software tools that will be accessible for users to apply scientifically proven linguistics rules in order to automatically process data from predetermined data sets in order to derive scientifically supportable conclusions pertaining to the data. The software products will utilize technologies that can review and process large data sets, and apply rules of logic to reach required determination. Intuitive and simple to use User Interfaces will be applied to allow non-sophisticated users access and use of the software tools. FLINT has offices in the USA and in Denmark. This position will be located in Denmark, as part of our new technology center. Employment Type Full Time Industries: Computer Software, Internet, Data Analytics Job Description Data Scientists at FLINT are responsible for (i) providing guidance and aiding with algorithm development for a text-mining product that uses advanced linguistic rules to make decisions around authorship (ii) converting raw data, usually text, into actionable insights for our customers as well as internal decision makers and stakeholders. This role will report to the company s senior executives and product-leads, and is expected to own data science for FLINT s new Authorship product. The Authorship product provides tools to help identify and profile authors based on their writing samples. We do this by leveraging the latest advances in data science and computational linguistics to bring forward predictions and insights on the writing style and consistency of different authors, enabling our customers to make better decisions about the origin of a piece of writing with more context and clarity. Role And Responsibilities Work closely with subject matter experts and product engineers. Find, extract, and clean text data to answer questions by writing efficient and robust SQL queries, Python, and or R code. Develop innovative and rigorous statistical aggregation and modeling techniques to make predictions and extract insights from the data. Regularly communicate project direction, status, needs and key findings to stakeholders across the company, from teammates and colleagues to senior and executive leadership. Stay up to date with the latest advances in applied data science by reading papers, industry blogs, and attending conferences. Function as a Data Science thought leader within FLINT, helping to champion good data practices and expand the vision of data science across the company. Mentor more junior data scientists as the team grows. Requirements Fluency in SQL, Python Jupyter notebooks or R RStudio, unix systems, git, github. Strong applied knowledge of Statistics and predictive algorithms and fluency with general machine learning domains including classification, regression and unsupervised clustering. Prior experience in text analysis, natural language processing, or computational linguistics. Strong data science and data exploration skills in local and cloud-based workflows. Advanced degree in Statistics, Applied Mathematics, or related field or 3 years of relevant industry experience. Knowledge of and experience with computer science, text data mining and algorithm development, preferred. Fluency in English Ability to drive and manage local and or remote projects products Apply This job is posted through Yang IT Consulting ApS, which helps FLINT Systems looking for a Data Scientist. Please kindly submit your application to resumes@flintai.com

Summary

FLINT Systems is a data analytics technology firm whose mission is to develop technologies based in computational linguistics to automatically process textual data for the purposes of authorship analysis.

FLINT is a new technology start up that will focus its efforts upon the development of innovative technologies that will be used for purpose of forensic linguistic analysis.  FLINT Forensic Linguistic software will be SaaS based software tools that will be accessible for users to apply scientifically proven linguistics rules in order to automatically process data from predetermined data sets in order to derive scientifically supportable conclusions pertaining to the data.  The software products will utilize technologies that can review and process large data sets, and apply rules of logic to reach required determination.  Intuitive and simple to use User Interfaces will be applied to allow non-sophisticated users access and use of the software tools.  

FLINT has offices in the USA and in Denmark.  This position will be located in Denmark, as part of our new technology center.

Employment Type

Full Time

Industries:

Computer Software, Internet, Data Analytics

Job Description

Data Scientists at FLINT are responsible for (i) providing guidance and aiding with algorithm development for a text-mining product that uses advanced linguistic rules to make decisions around authorship; (ii) converting raw data, usually text, into actionable insights for our customers as well as internal decision makers and stakeholders.

This role will report to the company’s senior executives and product-leads, and is expected to own data science for FLINT’s new Authorship product. The Authorship product provides tools to help identify and profile authors based on their writing samples. We do this by leveraging the latest advances in data science and computational linguistics to bring forward predictions and insights on the writing style and consistency of different authors, enabling our customers to make better decisions about the origin of a piece of writing with more context and clarity.

Role And Responsibilities

  • Work closely with subject matter experts and product engineers.
  • Find, extract, and clean text data to answer questions by writing efficient and robust SQL queries, Python, and/or R code.
  • Develop innovative and rigorous statistical aggregation and modeling techniques to make predictions and extract insights from the data.
  • Regularly communicate project direction, status, needs and key findings to stakeholders across the company, from teammates and colleagues to senior and executive leadership.
  • Stay up to date with the latest advances in applied data science by reading papers, industry blogs, and attending conferences.
  • Function as a Data Science thought leader within FLINT, helping to champion good data practices and expand the vision of data science across the company.
  • Mentor more junior data scientists as the team grows.

Requirements

  • Fluency in SQL, Python + Jupyter notebooks or R + RStudio, unix systems, git, github.
  • Strong applied knowledge of Statistics and predictive algorithms and fluency with general machine learning domains including classification, regression and unsupervised clustering.
  • Prior experience in text analysis, natural language processing, or computational linguistics.
  • Strong data science and data exploration skills in local and cloud-based workflows.
  • Advanced degree in Statistics, Applied Mathematics, or related field; or 3+ years of relevant industry experience.
  • Knowledge of and experience with computer science, text data mining and algorithm development, preferred.
  • Fluency in English
  • Ability to drive and manage local and/or remote projects / products

Apply

This job is posted through Yang IT Consulting ApS, which helps FLINT Systems looking for a Data Scientist. Please kindly submit your application to resumes@flintai.com 

Yang IT Consulting ApSVirum2019-09-26T00:00:002019-11-19T00:00:00
da-DK

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