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Cro Biostatistician Jobs in Raleigh, NC (NOW HIRING)

micro1 AI

Biostatistician

Raleigh, NC · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Durham, NC · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Biostatistician

Cary, NC · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

MMS

Senior Biostatistician - Remote (US)

Raleigh, NC · On-site

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... Senior Biostatistician: Responsibilities: * Create randomization and kit schedules independently ...

micro1 AI

Director of Biostatistics

Cary, NC · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Director of Biostatistics

Durham, NC · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Director of Biostatistics

Raleigh, NC · Remote

$60 - $65/hr

Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor, CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

MMS

Study Design Statistician (US)

Raleigh, NC · On-site

MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... We address the emerging analytics needs of the Industry with our biostatistics services, bespoke ...

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How much do cro biostatistician jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for cro biostatistician in Raleigh, NC is $55.94, according to ZipRecruiter salary data. Most workers in this role earn between $39.47 and $62.64 per hour, depending on experience, location, and employer.

What is a CRO biostatistician?

CRO Biostatisticians are statistical experts who work at Contract Research Organizations (CROs) to design, analyze, and interpret data from clinical trials and other research studies for pharmaceutical, biotechnology, and medical device companies. They ensure that studies are statistically sound and compliant with regulatory requirements. Their work is essential for determining the safety and efficacy of new drugs or treatments, and they collaborate closely with clinical teams, data managers, and regulatory agencies. CRO Biostatisticians also play a key role in preparing statistical analysis plans and contributing to regulatory submissions.

What are some common challenges faced by CRO biostatisticians when collaborating with cross-functional teams during clinical trials?

CRO Biostatisticians often work closely with clinical, data management, and regulatory teams, which can present challenges such as aligning statistical analysis plans with evolving study protocols, managing large and complex datasets, and ensuring clear communication of statistical concepts to non-statistical colleagues. Effective collaboration is essential, as miscommunication can impact timelines or data quality. Developing strong interpersonal and project management skills can help Biostatisticians navigate these challenges and contribute to successful clinical trial outcomes.

What are the key skills and qualifications needed to thrive as a CRO biostatistician, and why are they important?

To thrive as a CRO Biostatistician, you need a strong background in statistics, mathematics, and clinical research, typically supported by a master's or doctoral degree in biostatistics or a related field. Proficiency in statistical analysis software such as SAS, R, and understanding of CDISC standards are commonly required, along with knowledge of regulatory guidelines. Strong analytical thinking, attention to detail, and effective communication skills help in interpreting complex data and collaborating with multidisciplinary teams. These skills ensure the accuracy and integrity of clinical trial analyses, supporting regulatory submissions and successful drug development.

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Cro Biostatistician jobs near you
Infographic showing various Cro Biostatistician job openings in Raleigh, NC as of July 2026, with employment types broken down into 2% Internship, 82% Full Time, 8% Part Time, 4% Temporary, 3% Contract, and 1% Nights. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $116,354 per year, or $55.9 per hour.

Biostatistician

micro1 AI

Raleigh, NC • Remote

$60 - $65/hr

Part-time

Re-posted 4 days ago

Job description

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.

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