911 Biostatistics Jobs - Page 12

The Senior Biostatistician is responsible for leading, developing, implementing, and overseeing statistical strategies and deliverables in support of the Client’s R&D sponsored clinical trials. Under the guidance of Head of Biostatistics, this role contributes to the planning, execution and interpretation of statistical analyses across development programs, ensuring high-quality, timely deliverables that meet regulatory and scientific standards. Essential Functions Serve as biostatistics leader for assigned studies and projects Lead or contribute to study design discussions, including protocol development, endpoint definition, and sample size estimation Author and review Statistical Analysis...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

Who Are You? An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead Phase II-III clinical studies across your region. You are excited and enthusiastic, motivate your teams to do great work and collaborate easily with your clients. You never settle for what it is but always push clinical development forward to what it could be. You motivate others to do the same. Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Biostatistician you will be dedicated to one of ...

Who Are You? An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead Phase II-III clinical studies across your region. You are excited and enthusiastic, motivate your teams to do great work and collaborate easily with your clients. You never settle for what it is but always push clinical development forward to what it could be. You motivate others to do the same. Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Biostatistician you will be dedicated to one of ...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Works highly independent and performs critical assessments in collaboration with study teams or other departments to determine best approaches to manipulate subject data. The Assoc. Patient Data Specialist is capable of leading active and challenging interdepartmental discussions to explore best strategies and practices after understanding trial specific needs and diverse data bases that can be used as source of information. Reviews subject data from multiple sources with a data analytic mindset, capable of identifying trends, risks, gaps and areas for optimization as the subject data and the trial develops. Prepares and analyz...

Choosing Capgemini means choosing a place where you’ll be empowered to shape your career, supported by a collaborative global community, and inspired to reimagine what’s possible. Join us in helping leading healthcare and life sciences organizations unlock the value of data and drive evidence-based, impactful research. Your Role As a Statistical Programmer II at Capgemini, you will be responsible for programming and validating clinical trial data displays, datasets, and documentation in alignment with regulatory standards. You’ll collaborate with cross-functional teams and contribute to the delivery of high-quality statistical outputs for clinical research. In this role, you will: Program ta...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Collaborate with cross-functional teams to ensure timely and accurate data delivery. Conduct statistical review of case report forms, annotated CRFs, database structures, and study-related documentation. Provide statistical input into protocol development and review. Ensure compliance with regulatory requirements and company policies. Mentor junior statisticians and provide guidance on statistical methodologies. Job Requirements Strong knowledge of statistical concepts, including regression, time series, mixed effects, and predictive modeling. Experience with statistical software packages such as S...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Provide statistical input into protocol development and review. Ensure compliance with regulatory requirements and company policies. Mentor junior statisticians and provide guidance on statistical methodologies. Job Requirements Strong knowledge of statistical concepts, including regression, time series, mixed effects, and survival analysis. Experience with statistical software packages such...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Collaborate with cross-functional teams to ensure timely and accurate data delivery. Conduct statistical reviews of case report forms, annotated CRFs, database structures, and study-related documentation. Provide statistical input into protocol development and review. Ensure compliance with regulatory requirements and company policies. Mentor junior statisticians and provide guidance on statistical methodologies. Job Requirements Strong knowledge of statistical concepts, including regression, time series, mixed effects, and survival analysis. Experience with statistical software packages such as SA...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

Summary The SrGPSL-TL serves as strategic leader of the Medical Safety organization to improve patients’ lives and impact on overall Novartis results through robust safety risk management. This role requires an experienced and knowledgeable safety clinician responsible to predict safety risks and assess scientific information to guide the assigned teams on strategic considerations, effective risk management and overall positive impact in development programs. Ensures optimal patient safety for assigned compounds, is responsible for the integration, analysis, and interpretation of internal and external safety information from all sources through lifecycle management. This is a management posi...

The University of Hong Kong Apply now Ref.: 533275 Work type: Full-time Department: School of Public Health (22400) Categories: Research Staff Hong Kong Senior Research Assistant/Research Assistant I/II (holding the functional title of Senior Data Analyst/Data Analyst) (several posts) in the Division of Community Medicine and Public Health Practice, School of Public Health (Ref.: 533275) (to commence as soon as possible on a one-year temporary basis or two-year fixed-term basis, with the possibility of renewal subject to satisfactory performance) Applicants to the Senior Research Assistant post should possess a Bachelor’s degree or above in statistics, biostatistics, or related disciplines, ...

About the Role We are seeking a Clinical Data Co-ordinator to take ownership of data management activities for our ongoing clinical studies. The role requires end-to-end responsibility for data collection, cleaning, storage, quality control, and preparation of datasets for analysis, ensuring accuracy, integrity, and compliance with research standards. Key Responsibilities Ensure timely, accurate, and complete data entry and validation. Perform data cleaning, query management, and discrepancy resolution. Prepare data reports, summaries, and datasets for interim and final analyses. Collaborate closely with clinical investigators, study coordinators, and statisticians to support study outcomes....

Develop and implement statistical analysis plans for clinical trials. Conduct statistical programming activities, including data management, reporting, and visualization. Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Provide statistical guidance and support to junior staff members. Participate in project meetings and contribute to the development of project plans. Ensure compliance with regulatory requirements and company standards. Job Requirements Strong knowledge of biostatistics and statistical programming principles. Experience with statistical software packages, such as SAS or R. Excellent analytical and problem-solving skills, with attentio...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Conduct data review and quality control checks to ensure accuracy and completeness. Collaborate with cross-functional teams to design and execute statistical protocols. Provide statistical guidance and support to junior staff members. Review and approve statistical deliverables such as reports and presentations. Stay up-to-date with industry trends and developments in biostatistics and statistical programming. Job Requirements Strong knowledge of biostatistics and statistical programming principles. Experience working with clinical trial data and statistical software packages. Excellent analytical ...

About Viatris VIATRIS™ , is a new kind of healthcare Company, committed to providing access to medicines, advancing sustainable operations developing innovative solutions, and leveraging our collective expertise to improve patient outcomes. Formed in 2020, through the combination of Mylan and Up-John-Pfizer, Viatris bring together best in class scientific, Manufacturing and distribution expertise with proven regulatory, Medical and commercial capabilities to deliver quality medicines to patients when and where they need it. Fast Facts Headquartered in the US with global centers in Pittsburgh (USA), Hyderabad (India) and Shanghai (China) Our global workforce of ~37000, includes expertise acro...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials. Conduct data review and quality control checks to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams, including medical writing, biostatistics, and project management. Provide statistical guidance and support to junior staff members. Participate in developing and implementing new statistical methodologies and technologies. Ensure timely delivery of high-quality results and meet project deadlines. Job Requirements Strong knowledge of statistical concepts, including regression, time series, and mixed effects models. Experience with statistical softwar...

About the job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main responsibilities: The Senior Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QCd data packages incl...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials, ensuring compliance with regulatory requirements. Collaborate with cross-functional teams to design and conduct statistical programming activities, including data management and reporting. Provide statistical expertise and guidance to junior staff members, promoting knowledge sharing and skill development. Conduct quality control checks on statistical deliverables, ensuring high standards of accuracy and attention to detail. Participate in project meetings and discussions, providing input on statistical aspects of projects and representing the views of stakeholders. Stay updated with industry trend...

Roles and Responsibility Develop and implement statistical analysis plans for clinical trials, ensuring compliance with regulatory requirements. Collaborate with cross-functional teams to design and conduct statistical reviews of clinical trial protocols, informed consent forms, and case report forms. Provide statistical input on study design, sample size calculations, and statistical methodologies. Conduct statistical review of protocol deviations and ensure timely resolution. Develop and maintain databases for tracking and managing statistical data from clinical trials. Prepare and present reports on statistical findings and recommendations to stakeholders. Job Requirements Master's degree...

Director, Data Insights & Automation Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials. Job Summary Direct the development and maintenance of the required systems, infrastructure, and personnel to enable reliable, cost effective, automation and machine learning solutions available within SDC and to external partners and c...

Principal Biostatistician Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials. Job Summary Apply a high level of technical expertise to help guide and develop the more junior biostatistics staff members. Serve as a lead statistician on clinical studies and provide senior level peer review of work being accomplished by other...

Principal Clinical Programmer (RAVE EDC) Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials. Job Summary Lead in the evaluation, implementation, and validation of packaged systems. Create, maintain, and oversee processes for providing end user support in EDC systems. Build studies and support other users to build studies i...