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Clinical Research Rater Remote Jobs in Alabama (NOW HIRING)

Director of Biostatistics

Huntsville, AL ยท Remote

$60 - $65/hr

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 ...

" "" Licensed Clinical Psychologist Wage: Up to $151/hour Licensed Clinical Psychologists -- Are you ... Secure higher rates with top insurance plans through access to our nationwide insurance network ...

$151/hr

" "" Licensed Clinical Psychologist Wage: Up to $151/hour Licensed Clinical Psychologists -- Are you ... Secure higher rates with top insurance plans through access to our nationwide insurance network ...

$35.99 - $56.68/hr

Actual hourly rate dependent upon experience. $35.99 - $56.68 We care about your well-being - mind ... If applying for a remote or hybrid role, this includes remote work expectations related to ...

Remote Pharmacist

Birmingham, AL ยท Remote

$54.50 - $65.50/hr

Uses remote connectivity to access clinical systems for all hospitals serviced. * Understands and ... Uses appropriate online resources to research and respond to drug information questions. * Reviews ...

" "" Licensed Clinical Social Worker (LCSW) Wage: Up to $127/hour Licensed Clinical Social Worker -- Are ... Secure higher rates with top insurance plans through access to our nationwide insurance network ...

$127/hr

" "" Licensed Clinical Social Worker (LCSW) Wage: Up to $127/hour Licensed Clinical Social Worker -- Are ... Secure higher rates with top insurance plans through access to our nationwide insurance network ...

Evaluate and synthesize findings from biological, chemical, and clinical data sources. * Offer ... Proven track record of contributing to research projects at the intersection of biology, chemistry ...

Showing results 21-40

Clinical Research Rater Remote information

What is a clinical research rater?

A Clinical Research Rater (Remote) is a professional who works from a remote location to assess and evaluate participants in clinical research studies. They are responsible for administering psychological or cognitive assessments, interviews, and questionnaires to study subjects according to research protocols. The data they collect is used to determine the effectiveness and safety of medical treatments or interventions being studied. This position requires strong attention to detail, excellent communication skills, and the ability to follow standardized procedures. Remote raters typically collaborate with research teams via secure digital platforms and may require specific certifications or training.

What are the key skills and qualifications needed to thrive as a clinical research rater?

To thrive as a Clinical Research Rater (Remote), you need a background in psychology, neuroscience, or a related field, along with experience in clinical research and administering standardized assessments. Familiarity with electronic data capture (EDC) systems, clinical trial protocols, and certifications such as Good Clinical Practice (GCP) are highly valued. Attention to detail, strong organizational skills, and the ability to communicate clearly with research teams are crucial soft skills. These abilities ensure accurate data collection, adherence to study protocols, and high-quality research outcomes in a remote environment.

What are some typical challenges faced by remote clinical research raters, and how can they be addressed?

Remote Clinical Research Raters often face challenges such as maintaining consistent communication with study teams and ensuring accurate, unbiased assessments when working independently. To address these, it's important to establish clear protocols for virtual collaboration, regularly attend team meetings, and utilize secure data management systems. Staying organized and proactively reaching out for clarification when needed can help maintain high-quality data collection and foster a supportive remote work environment.

What is the difference between Clinical Research Rater Remote vs Clinical Data Entry Specialist?

AspectClinical Research Rater RemoteClinical Data Entry Specialist
Required credentialsHigh school diploma or equivalent; some roles may require clinical or research experienceHigh school diploma or equivalent; data entry skills preferred
Work environmentRemote, flexible hours, often part-timeRemote or on-site, regular hours, often full-time
Employer and industry usagePharmaceutical companies, research organizations, clinical trial sitesHealthcare providers, research organizations, hospitals

While both roles involve working remotely in the healthcare and research industry, Clinical Research Rater Remote focuses on evaluating patient data and clinical outcomes, whereas Clinical Data Entry Specialists primarily input and manage clinical data. The roles differ in responsibilities, with the former emphasizing assessment and analysis, and the latter concentrating on data accuracy and entry.

What are popular job titles related to Clinical Research Rater Remote jobs in Alabama? For Clinical Research Rater Remote jobs in Alabama, the most frequently searched job titles are:
What job categories do people searching Clinical Research Rater Remote jobs in Alabama look for? The top searched job categories for Clinical Research Rater Remote jobs in Alabama are:
What cities in Alabama are hiring for Clinical Research Rater Remote jobs? Cities in Alabama with the most Clinical Research Rater Remote job openings:
Infographic showing various Clinical Research Rater Remote job openings in Alabama as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Director of Biostatistics

micro1 AI

Huntsville, AL โ€ข Remote

$60 - $65/hr

Part-time

Posted 6 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 โ€” 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.