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Senior Specialist Programmer, Late-Stage CVRM Biometrics

Ansök    Mar 13    Randstad AB    Biostatistiker
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 compe... Visa mer
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

Senior Specialist Programmer: Late-Stage CVRM Biometrics

Ansök    Mar 11    Randstad AB    Biostatistiker
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 comp... Visa mer
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.


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 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
Requirements for the role:


• Minimum educational level is a BSc degree in a relevant subject such as statistics, biostatistics, mathematics, computer science, life science or engineering.
• Expertise in drug development and clinical data standards (CDISC)
• Expertise in ADaM (specification writing, programming, define generation and ADRG)
• Expertise in analysis output programming (Tables, Figures etc.)
• Good written and spoken English.


Desirable for the role:


• Expertise in multiple programming software such as R or Python
• Project management experience
• Good collaboration, communication and influencing skills
• Experience from regulatory submissions


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.

About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Statistician / Statistical Programmer

Ansök    Maj 12    IQVIA AB    Biostatistiker
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 he... Visa mer
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

Join IQVIA’s Real-world Insights experts in Gotheburg!

Biostatistician , Gothenburg, Sweden 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 ... Visa mer
Biostatistician , Gothenburg, Sweden
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 Visa mindre

Associate Director

Medical & Payer Evidence Statistics Biopharmaceuticals Medical -Evidence-Real World Science & Digital Provides advanced biostatistical support. Writes and/or reviews statistical analysis plans, study design concepts and protocols. Displays sound level of competence in a range of statistical methodologies and will often act as a point of reference for others. Typical Accountabilities * Provide statistical expertise in the design, analysis and inter... Visa mer
Medical & Payer Evidence Statistics Biopharmaceuticals Medical -Evidence-Real World Science & Digital

Provides advanced biostatistical support. Writes and/or reviews statistical analysis plans, study design concepts and protocols. Displays sound level of competence in a range of statistical methodologies and will often act as a point of reference for others.


Typical Accountabilities

* Provide statistical expertise in the design, analysis and interpretation of secondary observational research studies and primary data collection clinical studies/trials in support of Biopharmaceuticals Medical & Payer evidence generation research activities.
* Provide expert advice in the analysis of real-world data for stakeholders in Epidemiology, Market Access / HEOR, Medical Affairs, and other functional areas.
* Provide statistical guidance on the development of Study Design Concepts, Protocols, Statistical Analysis Plans, Data Presentation Plans, Clinical Study Reports and publication activities in support of BPM clinical/observational study activities.
* Provide oversight of CRO analytic activities for outsourced BPM clinical/observational studies as needed, supporting the Study Lead in reviewing all analytical activities outsourced to external vendors, including analysis plans, review of interim/final results and publications development.


Requirements
Essential

* Graduate degree in Statistics, Biostatistics, or related quantitative fields (epidemiology, health outcomes, health informatics or health economics) or equivalent course work/ technical experience with experience in pharma/healthcare or other relevant discipline.
* MS with 8 years of experience or PhD with 5 years of experience in the design, analysis and reporting of clinical studies/trials in a pharmaceutical research or academic setting.
* Demonstrated ability to work collaboratively on cross-functional teams across global & functional boundaries, both internally and externally.
* Self-motivated with the ability to work independently to solve complex and challenging problems using innovative strategies while maintaining focus on quality.
* Excellent communication skills and ability to build strong relationships.


Highly Desired

* At least 5+ years-experience in RWE observational research study management and data analytics within pharmaceutical industry.
* Advanced knowledge of epidemiologic and/or health economics methods, (e.g., propensity score analysis, marginal structural modeling). Visa mindre