Harvard University
Healthcare
BiostatisticianII
“Biostatistician II at Harvard University. Skills: Biostatistics, Statistical analysis, Clinical trials. Act as a protocol statistician. Collaborate with medical researchers, senior statisticians, and epidemiologists on clinical trials and observational studies”
Industry & Context.
This position has a term date of November 30, 2027 with a likelihood of extension., Harvard University is unable to provide visa sponsorship for this position., Pre-Employment Screening: Identity, Education, The Harvard T. H. Chan School of Public Health does not provide visa sponsorship, now or in the future, for staff positions., Harvard University requires pre--employment reference checks and background screenings., This position has a 120 day orientation and review period., Individuals must meet work location sponsorship requirements prior to employment.
What They're Looking For.
Must Have
Master's Degree in Biostatistics, Statistics, or a closely-related field, 3+ years of related experience, Experience with statistical software (such as SAS, Stata, etc.)
Nice to Have
Two-year Master's Degree (MA/MS) program, Education may count towards experience, Statistical experience with multi-center clinical trials, or equivalent collaborative statistical experience, Highly specialized and technical knowledge of statistical analysis and principles including categorical data and censored failure time data analysis, Advanced computer skills and experience with major statistical computing packages, Experience with independently analyzing data from clinical trials using statistical techniques, Experience contributing to the writing of manuscripts, abstracts, and other publications documenting study findings, Experience in effectively collaborating with study chairs, medical officers, protocol specialists and database managers, Familiarity with medical terminology
What You'll Do.
Act as a protocol statistician
Collaborate with medical researchers
and epidemiologists on clinical trials and observational studies
Clinical trial and observational study review
Design and review of data collection forms
Stratification/randomization of statistical data
Statistical data analysis
Serve on internal CBAR committees
Take leadership roles in activities within CBAR and in a Project/Network
Heading a CBAR committee or working group
Acting as a Topic Resource support to training and guidance materials for CBAR
Providing technical support to a Network-level committee or working group
Maintain professional knowledge and expertise
Participate in peer review and critique of reports
Collaborate in resolution of technical problems
and final analyses of data
Determine proper summary statistics
and all other analysis considerations
Review the proposed study methodology
and all other related study factors of concept sheets and protocols
Recommend revisions and modifications
Determine and write statistical considerations for protocol documents and statistical analysis plans
Develop stratification and randomization materials
Collaborate with senior statisticians on methodological research
Oversee the development of data collection forms and proposed data management methods
Ensure integrity of data collection
and analysis techniques
Identify potential or actual administrative or scientific suggest and implement corrective action
Prepare periodic and ad hoc data status reports
Collaborate with clinicians and senior CBAR statisticians on manuscripts
and other publications documenting study findings
How You'll Work.
Team & Collaboration
Collaborate directly with medical researchers, senior statisticians, and epidemiologists; Collaborate with study chairs, medical officers, protocol specialists and database managers; Collaborate with clinicians and senior CBAR statisticians on manuscripts, abstracts, and other publications
Communication Scope
written communication skills; verbal communication skills
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