Remote Biostatistician

Biostatistician

$60 - $65/hourpay

Required Skills

sas

r

cdisc sdtm

cdisc adam

statistical analysis plan (sap) interpretation

survival analysis

mixed models

covariate adjustment

multiplicity control

estimand and missing-data strategies under ich e9(r1)

clinical trial data analysis

tables, figures, and listings (tfls) production and qc

regulatory submission preparation

statistical quality control

clinical study report (csr) review

documentation

written communication

collaboration

critical thinking

attention to detail

About micro1

micro1 is the leading AI data lab for training frontier models and evaluating AI agents. Experts contribute their diverse subject matter knowledge across domains such as finance, healthcare, STEM engineering, and more. micro1 transforms that real-world expertise into high-quality training data, evaluations, and feedback loops that improve how AI systems learn, reason, and perform.

Our platform identifies and vets top talent through an AI recruiter, enabling high-quality expert contributions at scale. We aim to enable 1 billion people to do meaningful work by applying their expertise to AI. As our global expert network grows, micro1 is building the human intelligence layer for frontier AI.

Role Title: Biostatistician

Role Type: Contractor

Location: Remote

micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.

Scope of Work

1. Author and review evaluation tasks that require deriving, reproducing, or validating statistical outputs from clinical datasets and associated tables, figures, and listings (TFLs).
2. Apply expert judgment to assess the correctness and consistency of reported estimates, confidence intervals, p-values, analysis populations, and missing data handling in alignment with the statistical analysis plan (SAP).
3. Identify discrepancies between statistical outputs and their narrative descriptions in clinical study reports (CSR), including subtle errors in population definitions, censoring rules, or multiplicity handling.
4. Establish defensible ground truth for each evaluation task, documenting the derivation process to enable independent verification.
5. Provide structured written rationales distinguishing true statistical errors from acceptable methodological alternatives, employing clear and concise communication.
6. Collaborate with a multidisciplinary project team, providing statistical insights and feedback as needed to refine evaluation tasks and criteria.

Preferred Qualifications

1. 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit.
2. Hands-on experience producing or quality controlling TFLs for regulatory submissions and working directly from CDISC SDTM/ADaM datasets.
3. Solid understanding of statistical methods used in confirmatory trials, including survival analysis, mixed models, covariate adjustment, multiplicity control, and estimand and missing-data strategies under ICH E9(R1).
4. Proficiency in SAS and/or R, with the ability to independently reproduce analyses from written specifications.
5. Ability to interpret SAPs and ensure reported results are consistent with pre-specified analyses.
6. Advanced degree (MSc or PhD) in Biostatistics, Statistics, or a closely related quantitative field.
7. Nice to have: Experience as lead statistician on pivotal/registrational studies, authoring or reviewing CSR statistical sections, oncology endpoint expertise, and exposure to AI-assisted statistical review tools.