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Remote Clinical Study Start Up Jobs in Indiana (NOW HIRING)

micro1 AI

Director of Biostatistics

Indianapolis, IN · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... study reports (CSR), including subtle errors in population definitions, censoring rules, or ...

micro1 AI

Biostatistician

Evansville, IN · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... study reports (CSR), including subtle errors in population definitions, censoring rules, or ...

micro1 AI

Director of Biostatistics

Evansville, IN · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... study reports (CSR), including subtle errors in population definitions, censoring rules, or ...

micro1 AI

Biostatistician

Fort Wayne, IN · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... study reports (CSR), including subtle errors in population definitions, censoring rules, or ...

micro1 AI

Director of Biostatistics

Fishers, IN · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... study reports (CSR), including subtle errors in population definitions, censoring rules, or ...

micro1 AI

Biostatistician

Fishers, IN · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... study reports (CSR), including subtle errors in population definitions, censoring rules, or ...

koch

Field Control Technician

Evansville, IN · Remote

$110K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Field Control Technician (Start-up & Commissioning) NOW HIRING - Field Control Technician (Start-up & Commissioning) | $110,000-$140,000/yr + Travel Per Diem Location: Remote, U.S.-based -- must ...

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Remote Clinical Study Start Up information

Can you do clinical research virtually?

Remote clinical study start-up roles can involve virtual work, especially with the increasing use of digital tools and electronic data capture systems. Many tasks, such as site identification, regulatory document preparation, and communication with study sites, can be performed remotely, though some activities may require in-person visits or site monitoring. Strong organizational skills and familiarity with remote collaboration platforms are important for success in virtual clinical research roles.

How to start a career in remote clinical study start up?

To start a career in remote clinical study start-up, gain relevant education such as a degree in life sciences, healthcare, or related fields, and develop knowledge of clinical trial processes and regulations. Experience with project management tools, good communication skills, and understanding of regulatory requirements like GCP are valuable. Entry-level roles often require certification or training in clinical research, and remote work may demand strong organizational skills and self-motivation.

What is the difference between Remote Clinical Study Start Up vs Remote Clinical Data Coordinator?

AspectRemote Clinical Study Start UpRemote Clinical Data Coordinator
Primary ResponsibilitiesPlanning, site selection, regulatory submissions, site initiationData entry, data validation, database management, data quality assurance
Required CredentialsLife sciences degree, knowledge of GCP, regulatory knowledgeLife sciences or related degree, familiarity with clinical data systems
Work EnvironmentCollaborates with sponsors, sites, regulatory bodiesWorks mainly with data management teams and databases
Industry UsageInvolved early in trial setup phasesInvolved during data collection and analysis phases

Remote Clinical Study Start Up focuses on preparing and initiating clinical trials, including site selection and regulatory compliance. In contrast, Remote Clinical Data Coordinator manages and ensures the accuracy of clinical trial data during the study. Both roles require related credentials and work within the clinical research industry, but they operate at different stages of the trial process.

What are the most commonly searched types of Clinical Study Start Up jobs in Indiana?

The most popular types of Clinical Study Start Up jobs in Indiana are:

What are popular job titles related to Remote Clinical Study Start Up jobs in Indiana?

For Remote Clinical Study Start Up jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Study Start Up jobs in Indiana look for?

The top searched job categories for Remote Clinical Study Start Up jobs in Indiana are:

What cities in Indiana are hiring for Remote Clinical Study Start Up jobs?

Cities in Indiana with the most Remote Clinical Study Start Up job openings:

Remote Clinical Study Start Up jobs near you
Infographic showing various Remote Clinical Study Start Up job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 63% Full Time, 16% Part Time, and 20% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Director of Biostatistics

micro1 AI

Indianapolis, IN • Remote

$60 - $65/hr

Part-time

Posted 11 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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