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Remote Merck Clinical Trials Jobs in Indiana (NOW HIRING)

Biostatistician

Indianapolis, IN ยท Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Biostatistician

Carmel, IN ยท Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Director of Biostatistics

South Bend, IN ยท Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Biostatistician

South Bend, IN ยท Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Director of Biostatistics

Fort Wayne, IN ยท Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Director of Biostatistics

Fishers, IN ยท Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Biostatistician

Fishers, IN ยท Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Director of Biostatistics

Evansville, IN ยท Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Biostatistician

Evansville, IN ยท Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... Preferred Qualifications * 5+ years as a biostatistician supporting clinical trials at a sponsor ...

Hematologist / Oncologist

Indianapolis, IN ยท Remote

$160 - $200/hr

Clinician (Oncology / Hematology) Role Type: Contractor Location: Remote micro1 is engaging ... Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical ...

Hematologist / Oncologist

Fishers, IN ยท Remote

$160 - $200/hr

Clinician (Oncology / Hematology) Role Type: Contractor Location: Remote micro1 is engaging ... Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical ...

Hematologist / Oncologist

Carmel, IN ยท Remote

$160 - $200/hr

Clinician (Oncology / Hematology) Role Type: Contractor Location: Remote micro1 is engaging ... Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical ...

Hematologist / Oncologist

Evansville, IN ยท Remote

$160 - $200/hr

Clinician (Oncology / Hematology) Role Type: Contractor Location: Remote micro1 is engaging ... Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical ...

Hematologist / Oncologist

South Bend, IN ยท Remote

$160 - $200/hr

Clinician (Oncology / Hematology) Role Type: Contractor Location: Remote micro1 is engaging ... Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical ...

Hematologist / Oncologist

Fort Wayne, IN ยท Remote

$160 - $200/hr

Clinician (Oncology / Hematology) Role Type: Contractor Location: Remote micro1 is engaging ... Direct involvement in clinical trials as investigator, sub-investigator, or sponsor-side medical ...

Showing results 21-40

Remote Merck Clinical Trials information

What are the key skills and qualifications needed to thrive as a remote clinical trials specialist at Merck?

To excel as a Remote Clinical Trials Specialist at Merck, you generally need a background in life sciences or healthcare, experience in clinical research, and familiarity with Good Clinical Practice (GCP) guidelines. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and sometimes certifications like SOCRA or ACRP are commonly required. Strong organizational skills, attention to detail, and effective remote communication are essential soft skills for managing study protocols and collaborating with diverse teams. These competencies are crucial for ensuring regulatory compliance, data integrity, and the efficient coordination of clinical research activities from a remote setting.

What is a remote Merck clinical trial?

Remote Merck Clinical Trials are research studies conducted by Merck & Co., Inc. that allow participants to take part from their homes or other locations outside of traditional clinical sites. These trials use digital technologies, such as telemedicine, mobile apps, and wearable devices, to monitor participants, collect data, and communicate with study teams. Remote trials aim to make participation more convenient, increase patient diversity, and improve data collection. They may include virtual visits, home delivery of study medications, and remote monitoring of health outcomes. This approach helps expand access to clinical research while maintaining the safety and integrity of the study.

What is the difference between Remote Merck Clinical Trials vs Remote Clinical Research Associate?

AspectRemote Merck Clinical TrialsRemote Clinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonSame as Merck Clinical Trials, often requiring similar degrees and certifications
Work EnvironmentRemote, often within pharmaceutical or biotech companies like MerckRemote, working on clinical trial sites or for research organizations
Employer & Industry UsagePrimarily employed by pharmaceutical companies like Merck, focusing on clinical trial managementEmployed by CROs or pharmaceutical companies, focusing on site monitoring and trial coordination

Both roles involve clinical trial work with similar credentials and work environments. The main difference is that Remote Merck Clinical Trials refers to roles within Merck's clinical trial programs, while Remote Clinical Research Associates typically work across various organizations, focusing on site monitoring and trial coordination.

How do remote team members in Merck clinical trials collaborate with on-site staff and ensure seamless trial operations?

Remote team members in Merck Clinical Trials utilize secure digital platforms for communication, data management, and document sharing to stay connected with on-site colleagues. Regular virtual meetings, clear scheduling, and standardized protocols help bridge the distance and maintain alignment on clinical trial milestones. Collaboration tools such as electronic trial master files (eTMF) and project management software are commonly used to track progress and address challenges promptly. This structure enables remote staff to contribute effectively to trial operations, support patient recruitment, and monitor compliance while maintaining efficiency and strong team integration.
What are the most commonly searched types of Merck Clinical Trials jobs in Indiana? The most popular types of Merck Clinical Trials jobs in Indiana are:
What are popular job titles related to Remote Merck Clinical Trials jobs in Indiana? For Remote Merck Clinical Trials jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Remote Merck Clinical Trials jobs? Cities in Indiana with the most Remote Merck Clinical Trials job openings:
Infographic showing various Remote Merck Clinical Trials job openings in Indiana as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

Biostatistician

micro1 AI

Indianapolis, IN 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.