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Clinical Research Associate Cro Jobs in Normal, AL

micro1 AI

Biostatistician

Huntsville, AL · Remote

$60 - $65/hr

... clinical research. In this role, you'll apply your expertise to help train next-generation AI ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

micro1 AI

Director of Biostatistics

Huntsville, AL · Remote

$60 - $65/hr

... clinical research. In this role, you'll apply your expertise to help train next-generation AI ... CRO, or academic trials unit. * Hands-on experience producing or quality controlling TFLs for ...

Guidehouse

Associate Epidemiologist

Huntsville, AL · On-site

$53K - $88K/yr

... research, and data modernization initiatives as part of our Technology AI/Data capability. This ... Support epidemiologic analysis of surveillance, clinical, claims, survey, and other public health ...

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All JobsClinical Research Associate Cro JobsClinical Research Associate Cro Jobs in Normal, AL

Clinical Research Associate Cro information

See Normal, AL salary details

$10

$36

$61

How much do clinical research associate cro jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for clinical research associate cro in Normal, AL is $36.50, according to ZipRecruiter salary data. Most workers in this role earn between $25.58 and $46.73 per hour, depending on experience, location, and employer.

What is the difference between Clinical Research Associate Cro vs Clinical Trial Assistant?

AspectClinical Research Associate CroClinical Trial Assistant
CredentialsBachelor's degree, often with certifications like CCRP or RACTypically a high school diploma or associate degree, with some roles requiring a certificate
Work EnvironmentConducts site visits, monitors trials, and ensures complianceSupports trial coordination, manages documentation, and assists with logistics
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, clinical trial teams

The Clinical Research Associate Cro focuses on monitoring clinical trials, ensuring compliance, and site management. In contrast, the Clinical Trial Assistant provides administrative support, manages documentation, and assists with trial logistics. Both roles are essential in clinical research but differ in responsibilities and required experience.

What cities near Normal, AL are hiring for Clinical Research Associate Cro jobs?

Cities near Normal, AL with the most Clinical Research Associate Cro job openings:

Clinical Research Associate Cro jobs near you

Biostatistician

Huntsville, AL • Remote

micro1 AI
Software Development • 11 - 50 employees
Learn more about micro1 AIexternal

$60 - $65/hr

Part-time

This job post has expired today. Applications are no longer accepted.

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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