Biostatistician
A biostatistician specializes in applying statistical methods to the analysis of biological data. They design experiments, analyze results, and contribute to findings in medical research and life sciences.
Biostatistician
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Sample Job Descriptions for Biostatistician
Below are the some sample job descriptions for the different experience levels, where you can find the summary of the role, required skills, qualifications, and responsibilities.
Junior (0-2 years of experience)
Summary of the Role
We are seeking a Junior Biostatistician to join our dynamic team in a role focused on statistical analysis of biological data. The successful candidate will support clinical trials and research studies by providing statistical expertise that ensures the integrity and validity of collected data.
Required Skills
  • Statistical analysis
  • Data management
  • Statistical software proficiency (SAS, R, Python)
  • Critical thinking
  • Communication
  • Collaboration
Qualifications
  • Bachelor's or Master's degree in Biostatistics, Statistics, Epidemiology, or a related field.
  • Demonstrated understanding of statistical concepts and methodologies.
  • Familiarity with statistical software such as SAS, R, or Python.
  • Ability to interpret and present statistical results effectively.
  • Strong problem-solving and analytical skills.
  • Excellent communication and teamwork abilities.
Responsibilities
  • Assist in the design of experiments and clinical trials.
  • Perform statistical analysis on biological data sets.
  • Contribute to the development of analysis plans and data reporting.
  • Support senior biostatisticians in the preparation of study reports and manuscripts.
  • Perform data management tasks, including data cleaning and validation.
  • Collaborate with a multidisciplinary team including researchers, clinicians, and data managers.
  • Keep abreast of new developments in biostatistics and apply them as appropriate.
Intermediate (2-5 years of experience)
Summary of the Role
As a Biostatistician, you will be responsible for applying statistical theory and methods to solve problems in biology, health sciences, and other life science disciplines. In this role, you will help design experiments, analyze and interpret data from clinical trials, and contribute to research findings that can advance medical knowledge and improve patient care.
Required Skills
  • Strong analytical and problem-solving skills.
  • Ability to manage and analyze large datasets.
  • Excellent attention to detail and precision.
  • Ability to work collaboratively in interdisciplinary teams.
  • Time management skills with the ability to meet project deadlines.
  • Critical thinking and logical reasoning abilities.
  • Proficiency in programming for data analysis.
Qualifications
  • Master's degree in Biostatistics, Statistics, or a related field.
  • 2-5 years of practical experience in biostatistics or a similar role.
  • Proficiency in statistical software such as SAS, R, or STATA.
  • Solid understanding of clinical trial design and analysis.
  • Experience in statistical modeling and survival analysis.
  • Knowledge of regulatory requirements pertaining to biostatistics in clinical research.
  • Excellent communication skills with the ability to present complex statistical concepts to non-statisticians.
Responsibilities
  • Design and analyze clinical trials and other types of biological experiments.
  • Develop statistical models to understand biological processes and diseases.
  • Interpret data and report findings to stakeholders, including writing statistical sections of study protocols.
  • Collaborate with scientists and researchers in developing new methodologies or improving existing ones.
  • Ensure compliance with regulatory standards for statistical analysis and reporting.
  • Perform sample size and power calculations for planned experiments.
  • Stay up-to-date with advancements in biostatistics and apply innovative statistical methods as appropriate.
Senior (5+ years of experience)
Summary of the Role
We are seeking a Senior Biostatistician to join our team, who will be responsible for leading statistical analysis projects and providing insights that inform our scientific and clinical research decisions. The ideal candidate will have a strong background in biostatistics, epidemiology, or a related field, with substantial experience in analyzing complex datasets and contributing to peer-reviewed publications.
Required Skills
  • Advanced statistical analysis and modeling
  • Proficient in SAS/R/Python statistical software
  • Data management and quality control processes
  • Clinical trial design and analysis
  • Regulatory submission and reporting requirements
  • Leadership and team collaboration
  • Strong problem-solving capabilities
  • Attention to detail and accuracy
Qualifications
  • Master's or PhD in Biostatistics, Statistics, or a related quantitative field.
  • Minimum of 5 years of relevant experience in biostatistics within the pharmaceutical, biotechnology, or healthcare industry.
  • Expertise in statistical programming languages such as SAS, R, or Python.
  • Demonstrated experience in the design and analysis of clinical trials.
  • Strong understanding of regulatory guidelines related to statistical analysis in clinical research.
  • Proven track record of contributing to peer-reviewed publications and presentations in the field.
  • Excellent communication and collaboration skills.
Responsibilities
  • Develop statistical analysis plans and perform statistical analyses for complex clinical trials and research projects.
  • Collaborate with cross-functional teams including clinical operations, data management, and regulatory affairs to ensure quality and integrity of data analysis.
  • Provide statistical expertise for study design, data interpretation, and results presentation.
  • Mentor junior biostatisticians and provide guidance on statistical methods and practices.
  • Stay current with the latest statistical methodologies and best practices in the field of biostatistics.
  • Prepare statistical sections of protocols, clinical study reports, and regulatory submissions.
  • Communicate statistical analysis findings to non-statistical colleagues and stakeholders.
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