Lediga jobb som Statistiker i Mölndal

Job description
Senior Specialist Programmer, Late-Stage CVRM Biometrics, AstraZeneca


Are you interested in becoming part of the group of statistical programming at AstraZeneca R&D? Late-stage Cardiovascular, Renal and Metabolism Biometrics is now looking for a Senior Specialist Programmer for a contract assignment with start as soon as possible.


This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities
Join a team of statisticians and statistical programmers to provide programming expertise to the design, conduct, reporting, interpretation, documentation, and regulatory submissions of our clinical development programs. Depending on your experience, you may contribute to more strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be a part of the function's adaptation and development of programming tools, standards, and processes.


About randstad life sciences
Randstad Life Sciences is specialized in competencies within Life Science. As a consultant with us, you get a competitive salary, benefits, and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many activities.


Deadline: 2024-03-21, selection and interviews will be ongoing. For more information: Please contact Katan Ali, [email protected]

Qualifications
Personal Qualities:


• Candidates should possess good social skills, be a strong team player and be able to work effectively in a global organization where teams often are geographically dispersed.
• You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude.
• It is essential to have good organizational and communication skills and you should be able to analyze and summarize your results and be comfortable in presenting them.
• Successful candidates will have the ability to communicate subject matter expertise to other experts, as well as an interest in the application of programming in pharmaceutical development.


Why AstraZeneca?


Join the team for unlocking the power of what science can do. You have the potential to grow yourself, our pipeline, and positively impact the lives of billions of patients around the world.


What’s next? If this sounds like your next challenge – welcome to apply!

About the company

Kelly Services (UK) Limited Visa mindre

Brinner du för miljö- och hållbarhetsfrågor? Är du nyfiken, driven och initiativrik och vill arbeta tillsammans med partners och kunder mot ett hållbart samhälle?

Om oss
Vår enhet Miljö och hållbar kemi expanderar inom livscykelanalysområdet och vi söker nu en medarbetare med erfarenhet av livscykelperspektivet för att bli en del av vårt team.

I vår verksamhet, lokaliserad i Mölndal och Stockholm, arbetar vi med frågor inom områdena cirkulär ekonomi, resurseffektivitet, livscykelanalys och hållbarhetsbedömning. Enheten är även hemvist för Substitutionscentrum och Kemikaliegruppen på RISE.

Om rollen
I din roll hos oss kommer du att arbeta med livscykelperspektiv och livscykelanalys i större projekt såväl som i direkta uppdrag mot kund. Vi arbetar mycket i team, men vi värdesätter även högt förmågan att ta egna initiativ och arbeta självständigt då en viktig del av vår verksamhet involverar initiering och ledning av projekt som svarar mot industrins behov. Som medarbetare på RISE har du stora möjligheter att forma dina arbetsuppgifter och bidra till ett hållbart samhälle, via uppdrag, men även i anslagsfinansierade projekt både nationellt och på EU-nivå.

För att lyckas i din roll ser vi att du har erfarenhet inom LCA-området, det kan handla om livscykelanalyser, miljövarudeklarationer (EPD), klimatavtryck och miljöutredningar utifrån ett livscykelperspektiv, men även att bidra med beslutsunderlag avseende produkt- och processförbättringar. Du kommer att medverka som LCA-specialist och utförare i våra projekt och kommer även att leda och driva projekt mot kund samt medverka vid försäljning av projekt. Du arbetar tillsammans med enhetens, och övriga RISE, kompetenta medarbetare, både i kortare uppdrag och i projekt som löper under ett antal år. Du tycker om att skapa nätverk, ser möjligheter och arbetar för att bidra till enhetens projekt- och uppdragsportfölj.

Viktiga arbetsuppgifter är:

- Kontakt med kunder, samarbetspartners och finansiärer
- Projektledning och initiering av nya projekt och uppdrag
- Livscykelanalys där datainsamling, modellering, beräkning och analys avseende miljöpåverkan ingår
- Bygga internt och externt nätverk

Placeringsort är Mölndal eller Stockholm.

Vem är du?
Vi söker dig som har ett stort intresse för miljö- och hållbarhetsfrågor och erfarenhet av arbete med livscykelanalys. Du har relevant akademisk utbildning och erfarenhet av att genomföra LCA och använda relevant mjukvara såsom SimaPro eller GaBi. Som person är du kundfokuserad och kommunikativ, och kan uttrycka dig väl i både tal och skrift på både svenska och engelska. Du är initiativrik och driven med god förmåga att arbeta självständigt såväl som i team. Forskarutbildning är meriterande.

Är vi rätt för varandra?
Inom RISE gillar vi olika och vi är övertygade om att mångfald bidrar till en innovativ miljö där vi tillsammans utmanar gränser och utvecklar ny kunskap och kompetens för framtiden. Hos oss möts passionerade problemlösare för att lösa några av världens viktigaste, och kanske roligaste, problem. Vi kan inte lova dig ett enkelt jobb, men vad vi kan lova dig är ett gäng engagerade kollegor och några riktigt spännande samhällsutmaningar att ta itu med. Du kommer att arbeta i en dynamisk miljö som ger dig utvecklingsmöjligheter både professionellt och personligt. Hos oss får du möjlighet att göra skillnad på riktigt. Välkommen till hela Sveriges forskningsinstitut och innovationspartner.

Välkommen med din ansökan!
Välkommen med din ansökan senast den 15 maj 2021. Vid frågor om tjänsten, kontakta enhetschef Lisa Schwarz Bour, tel: 010-228 48 07.

Våra fackliga representanter är Melina da Silva, Sveriges Ingenjörer, 010-228 46 96 och Elisabeth Olsson, Unionen, 010-228 47 67.

Vi har valt rekryteringskanaler för den här anställningen och vill inte bli kontaktade av rekryteringsföretag.

Livscykelanalys, hållbarhet, cirkulär ekonomi, resurseffektivitet, projektledning, miljö, RISE, Mölndal, Stockholm Visa mindre

Job description
Senior Statistical Programmer

The Senior Statistical Programmer II is a delivery focused role responsible for programming deliverables with quality and timeliness, following established standards and processes. This position requires high technical skills and thorough industry knowledge to independently perform the programming tasks while using judgement about seeking guidance in complex situations. They can be responsible for leading the programming deliveries of clinical studies or small to medium sized clinical projects and can lead cross-functional teams to deliver continuous improvement.

Responsibilities
Typical Accountabilities
Responsible for leading the programming deliveries of a clinical study or a small to medium sized and complex clinical project
Implements statistical programming aspects of the protocol or clinical development program
Ensures high quality is built into own deliverables and the quality delivered by other programmers
Programs independently with high efficiency and quality
Writes specifications and oversee completeness of relevant documentation
Contributes to or drives the development of best practices to improve quality, efficiency and effectiveness within function
Ensures compliance to standards and automation usage
Plans and leads team activities and tasks
Identifies, manages and communicates risk within the assigned studies and/or projects
Works proactively with study team members including but not limited to the statistician, lead programmer, data manager and study leader
Works cooperatively with contract programming providers
Influences stakeholders by providing subject matter expertise on programming related items
Contributes to or leads technical initiatives
Employs project management practices in managing programming aspects of drug or technical projects


Qualifications
Essential:
Degree in Mathematics (i.e., Applied Math, Engineering, etc), Statistics, Computer Science, Life Science or equivalent
Excellent programming skills including macro language • Proficient knowledge of the clinical development process
Thorough knowledge of industry standards
Ability to apply programming knowledge to problem solving
Ability to manage relevant documentation
Ability to influence relevant stakeholders on Programming related items

Desirable:
Ability to proactively manage concurrent activities within a study or part of project


Application
Deadline: 2022-03-17 , selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.

For more information:
Please contact Jimmy Wadie [email protected] or Veronika Knudsen [email protected]

About the company
Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many activities.

Randstad Life Sciences specializes in the field of science and is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Respiratory & Immunology portfolio

Hays Specialist Recruitment is now looking to recruit a Health Economics & Payer Evidence Lead to support the Respiratory & Immunology portfolio for a 1-year contract assignment at AstraZeneca in Gothenburg.

At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. We're focused on the potential of science to address the unmet needs of patients around the world. We commit to those areas where we think we can really change the course of medicine and bring big new ideas to life. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people's exceptional skills with those of people from all over the globe.

If you have in-depth knowledge of health economics and payer evidence requirements and its application to pharmaceutical development in the international environment, this is an opportunity to take on a role with a world-leading pharmaceutical company.

We're looking for a Health Economics & Payer Evidence Lead to join us in one of our Global R&D hubs to support our Respiratory & Immunology portfolio.

Main duties and accountabilities:
You will have a global leadership role and be responsible for shaping and delivering the evidence required to demonstrate the value of our products to payers and health authorities. You will collaborate with Clinical Development, Medical Evidence Generation, Observational Research, and Payer Teams in designing and implementing innovative health economic and payer evidence strategies and activities for target product profiles/claims, global payer evidence plans, and market access and pricing strategies. An equally important part of your role will be to lead or influence the production of scientific evidence for robust portfolio decisions, global reimbursement dossiers and reimbursement submissions to achieve market access.
You will proactively contribute to evidence planning, predict and resolve issues that affect market access decisions, and take responsibility for detailed strategic and tactical planning and implementation of payer evidence plans. Part of your remit will involve preparing proposals for outsourced health economics projects and collaborating with local market affiliates to prepare evidence that satisfies payer needs in their markets. You'll also represent health economics a payer evidence in cross-functional project teams to ensure that worldwide payer needs are reflected in drug development programs.

Essential requirements:

* Understanding of diverse pricing and reimbursement processes to maximize reimbursement opportunities through appropriate and timely payer evidence generation and analytics.
* Ability to influence without authority and being a strong collaborator. Experience collaborating across more than one function and understanding how this contributes to achieving business objectives
* Leadership skills and problem-solving capabilities, demonstrated by an ability to evaluate threats and opportunities for health economics strategies and modify them as appropriate
* Well-developed conceptual and integrative thinking with the capability to access internal and external resources for advice
* Ability to implement projects with a high degree of autonomy, including engaging key stakeholders.
* Ability to communicate technical material clearly in writing and oral presentations to both scientific and commercial audiences.
* Effective communication of sophisticated ideas for use with both payers and other partners.
* Knowledge of international healthcare systems and their changing needs for health economic and payer evidence.

Education, Training and Experience:

* Graduate / College degree in biomedical science, business, quantitative disciplines or economics
* Payer launch experience at a local or global level
* In-depth knowledge and technical capability in health economics and payer evidence needs, and its application to pharmaceutical development at an international level, especially economic modelling, evidence synthesis, clinical trial design and analyses and other analytical techniques required to support payer needs. Visa mindre

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.


IQVIA’s Real-world Insights experts deliver deep insights derived from statistical analyses of healthcare data through direct access to the world’s most comprehensive healthcare information, analytic and research resources. Our RWI team is made up of multi-disciplinary professionals, representing a variety of epidemiology-related disciplines from around the globe, that specialize in cutting edge and innovative analysis of healthcare data. Our diverse mix of clients, the breadth of disease areas, as well as the increasing access to novel data sources and advanced statistical methodologies, provide a constant and rewarding challenge for our team.


We are looking for a full-time STATISTICIAN/STATISTICAL PROGRAMMER to our Gothenburg office in Sweden to support our Real-World Evidence studies.


Your responsibilities can include:
- Contributing to planning of study designs for Real-World Evidence (RWE) projects
- Preparing statistical analysis plans
- Planning and conducting of statistical analysis using advanced R programming
- Participate in meetings with clients, in discussions around statistical methods and present analysis results
- Contribute to writing methods and results sections to study reports and publications


The exact responsibilities will be agreed individually based on the background and preference of the new employee.


With us you can be challenged and develop in a collaborative learning environment where you can have an impact on human health. We will support your development and career progression by providing career path opportunities as a part of global organization.


We are looking for candidates with the following qualifications:
- An academic degree (MSc) in statistics, applied mathematics, or related field
- Applicable several years’ experience in programming statistical analysis in R language for example within academia, pharmaceutical industry, contract research organization, or other relevant organization
- Experience of survival analysis and healthcare register data
- Strong communication and interpersonal skills, including fluent written and spoken English
- Ability to work in several projects in parallel, often under time pressure


Benefits
We offer a competitive salary along with other employee focused benefits for health and recreation. Our employees receive focused orientation training to ensure they are provided the best opportunities to perform their tasks. The working environment is vibrant with high-energy team collaboration and opportunities for personal growth and development in a research-orientated industry. With us you can develop, not only your own career, but also a growing international company.


For additional information about this position, please contact Anna Lundin, Manager, RWE Research, [email protected].


Please send your application in English by the 27th of May. Visa mindre

Om tjänsten
As a Statistical Programmer you would join a team of statistical programmers in Late Respiratory Biometrics and act as the main programmer of a Phase III trial in China and provide support in the rest of programming activities across the Aclidinium franchise.


Dina arbetsuppgifter i huvudsak
Candidates should possess good social skills, be strong team players and be able to work effectively in a global organization where teams often are geographically dispersed. You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude.

It is essential to have good organizational and communication skills and you should be able to analyze and summarize your results and be comfortable in presenting them. Successful candidates will have the ability to communicate subject matter expertise to other experts, as well as an interest in the application of programming in pharmaceutical development.


Vem är du?
Additional background
• Experience in Respiratory is desirable, expertise in China submissions and previous AZ experience would be ideal.
• Minimum educational level is a BSc degree in a relevant subject such as biostatistics, mathematics, computer science or life science.
• Minimum of 8 years SAS programming experience in the Pharma sector (CRO/industry).
• Expertise in CDISC standards (SDTMs, ADaM), TLFs production and CRT packages, as well as in regulatory submissions and regulatory defence activities.
• Good collaboration, communication, leadership and influencing skills.
• Good written and spoken English.

Om verksamheten
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Individuals are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. Visa mindre

Do you want to make a difference for millions of patients by applying your expertise in a global company that follows the science and turn ideas into life changing medicines? Join us now to be part of the development of future treatments of Cardiovascular, Renal and Metabolic diseases!
We are now recruiting Statisticians / Statistiker to join our growing late stage development CVRM Biometrics function at AstraZeneca’s dynamic R&D site in Gothenburg, Sweden. We are offering opportunities at different levels depending on your previous experience. We welcome your application both if you are in the very beginning of your career or if you have extensive experience from the pharmaceutical industry or other statistical applications.
You will join a dynamic team of statisticians and statistical programmers to provide statistical expertise to the design, planning, reporting, interpretation, documentation and regulatory submissions of our clinical development programs. You will also get the opportunity to do work of exploratory nature, e.g. modeling and simulation as well as other means to improve internal decision making. As a more experienced statistician you will be expected to contribute to strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be part of the function’s adaption and development of statistical methodology and praxis.
Key words: Statistiker, Biostatistiker, Statistik, Biostatistik
Requirements
As our work is conducted in cross functional project teams in an international environment, it is important that your statistical skills are combined with excellent inter-personal, collaboration and communication skills to be able to work effectively in a global organization where teams often are geographically dispersed.
The minimum required educational level is a M.Sc. degree in a relevant discipline such as statistics, biostatistics or mathematical statistics. Excellent English is also required, both written and spoken.
We value that you are a strong team player with a sincere interest in the application of statistical methodology in drug development. We also appreciate your interest in, and ability to, communicate statistical matters to other experts in other disciplines within AstraZeneca. In addition, you are able to work independently and take own initiatives with a positive, goal oriented and problem-solving attitude.
Other advantageous qualifications are: Post-graduate research degree, experience from drug development or other related fields, experience in using statistical software such as SAS or S-Plus/R.
We would like to know more about you. If you are interested to know more about us, apply now!
For more information about these positions please contact hiring manager Per Nyström at [email protected]
Welcome with your application no later than November 30th, 2019.
Additional information
Our Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
Culture and atmosphere of the Gothenburg site: https://www.linkedin.com/feed/update/urn:li:activity:6496327311678410752/
Life in Gothenburg and Sweden: https://www.movetogothenburg.com/
About AstraZeneca Gothenburg
Our stunning campus in Gothenburg is one of AstraZeneca’s three strategic science centers. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we’ve created a series of environments where innovation can happen. Visa mindre

Vi arbetar för rätten till sunda, säkra och utvecklade arbetsförhållanden. Vi driver på för att det på varje arbetsplats ska finnas ett aktivt arbetsmiljöarbete, där alla vill och kan bidra.

Dnr 2019/052421

Vill du arbeta med frågor som gör skillnad för hela arbetsmarknaden och som bidrar till en bättre arbetsmiljö, färre olyckor och tillbud för alla som arbetar i Sverige? Då kan detta vara något för dig!

Vi söker en Analytiker till Mölndal som ska, tillsammans med kunniga och engagerade medarbetare, arbeta mot osund konkurrens i arbetslivet. Du kommer att tillhöra enheten för statistik och analys och kommer därför ha din närmsta chef och flera av dina närmsta kollegor i Stockholm.


Ditt nya arbete
Du kommer att vara en viktig del i arbetet med myndighetsgemensam kontroll för att motverka fusk, regelöverträdelser och brottslighet i arbetslivet. Du kommer arbeta med analys och omvärldsbevakning, förberedelser inför olika typer av insatser, uppföljning och utveckling av arbetsmetoder och processer. Din roll kommer att till stor del vara koordinerande och samordnande, då du blir länken mellan analys och produktion. Du kommer även att delta i bedömningar om bidrag enligt förordningen om statsbidrag till arbetsmarknadens parter. Eftersom din närmsta chef och flera kollegor finns i Stockholm behöver du känna dij bekväm med digitala kommunikationsmedel och en del resor i tjänsten.


Kvalifikationskrav
Du ska ha högskoleutbildning med samhällsinriktning om minst 120 p enligt det gamla eller minst 180 hp enligt det nya högskolesystemet. Det ska ingå statistik och/eller matematik i din utbildning eftersom du kommer att arbeta med både kvalitativ och kvantitativ analys. Du kan också ha annan utbildning tillsammans med relevant arbetslivserfarenhet som arbetsgivaren bedömer som likvärdig. Du ska ha mycket god förmåga i det svenska och engelska språket i både tal och skrift. För att lyckas i uppdraget behöver du vara en mycket god lagspelare och ha mycket god kommunikativ förmåga. Du behöver vara strukturerad, prestigelös, lösningsorienterad och proaktiv. Du behöver också vara självgående, resultatinriktad, ha förmågan att utverka ett gott samarbete både internt och externt samt ha en personlig mognad och integritet.

Vid urvalet kommer vi att lägga stor vikt vid din personliga lämplighet.

Det är meriterande om du har: Erfarenhet av metodutveckling, samt arbetslivserfarenhet inom någon myndighet är meriterande.


Mer om anställningen
Anställningen är en tillsvidareanställning på heltid och är för närvarande placerad på Flöjelbergsgatan 2 i Mölndal. Vi har individuell lönesättning och tillämpar provanställning om 6 månader. Läs mer om vad vi erbjuder på vår hemsida av.se/arbeta hos oss. Arbetsmiljöverket erbjuder en attraktiv arbetsplats som utmärks av strävan att vara fri från diskriminering och ge lika möjligheter för alla. Att vi är olika bidrar till att verksamheten blir effektiv och för att kunna ta tillvara på varje medarbetares kompetens har vi ett inkluderande synsätt.

Som medarbetare tar du ansvar för dina arbetsuppgifter och bidrar till helheten genom att visa engagemang och hänsyn i samarbetet med andra. Du agerar efter våra värdeord trovärdig, kommunikativ och offensiv samt du har ett likabehandlingsperspektiv i din vardag. Tillsammans ska vi lyckas nå våra verksamhetsmål, bidra till en hälsosam arbetsmiljö och verka för en lärande arbetsplats.

Om du har frågor Kontakta oss på telefon 010-730 90 00. Frågor om anställningen besvaras av Ann Ponton Klevestedt, enhetschef statistik och analys. Fackliga kontaktpersoner är för SACO Hannes Kantelius och för ST Karl-Emil Sörensen.

Rekryteringen sköts av Arbetsmiljöverket och vi undanber oss säljsamtal från rekryteringsföretag och annonssäljare.  


Välkommen med din ansökan senast den 6 oktober 2019
Vi tar endast emot ansökningar via detta system. Ansök genom att klicka på länken nedan.


Om avdelningen
Avdelningen för administration och analys ansvarar för fyra av Arbetsmiljöverkets totalt nio verksamhetsområden: styra verksamheten, ge verksamhetsstöd, bedriva analysarbete och att hantera transfereringar. Vi ansvarar för kontakter med Regeringskansliet på tjänstemannanivå, regional skyddsombudsverksamhet och utstationeringsregistret. Inom avdelningen finns även svarstjänst, bland annat för allmänna frågor, e-tjänster och växel.

  Visa mindre