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Remote Clinical Study Startup Jobs in Indiana (NOW HIRING)

Beacon Talent

Credentialing Manager

Indianapolis, IN · Remote

$95K - $120K/yr

Remote (US) or Hybrid (City, State) Type: Full-time Reports to: Head of Operations / Director of ... Own end-to-end credentialing for clinicians/providers across multiple states and payers (as ...

NuVIEW Health, LLC

Telemedicine Cardiologist

Alexandria, IN · Remote

$310.10K - $350.40K/yr

This is a remote opportunity designed for experienced professionals who are passionate about ... Interpret diagnostic studies including EKG's echocardiograms and stress testing * Prescribe ...

NuVIEW Health, LLC

Telemedicine Cardiologist

Alexandria, IN · Remote

$310.10K - $350.40K/yr

This is a remote opportunity designed for experienced professionals who are passionate about ... Interpret diagnostic studies including EKG's echocardiograms and stress testing * Prescribe ...

Vaco LLC

VP, Provider Network

Crown Point, IN · Remote

$200K - $250K/yr

Company Size: small, startup style (under 60 people) Compensation: $200,000-250,000 Base DOE ... clinical and operational outcomes Partner with sales, account management, and product teams to ...

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Remote Clinical Study Startup information

What are the key skills and qualifications needed to thrive as a Remote Clinical Study Startup Specialist, and why are they important?

To thrive as a Remote Clinical Study Startup Specialist, you need a solid understanding of clinical trial processes, regulatory requirements, and project management, usually supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and regulatory submission platforms is essential. Strong organizational skills, attention to detail, and effective communication are vital soft skills for coordinating teams and ensuring timely study activation. These skills and qualities are crucial for maintaining compliance, minimizing delays, and driving successful clinical trial launches in a remote environment.

What are some common challenges faced in a Remote Clinical Study Startup role, and how can they be addressed?

Professionals in Remote Clinical Study Startup roles often encounter challenges such as coordinating documentation across multiple sites, ensuring regulatory compliance in different regions, and maintaining clear communication among dispersed teams. Successfully overcoming these hurdles typically involves leveraging robust digital tools for project management and document tracking, as well as establishing standardized communication protocols. Proactive problem-solving and strong organizational skills are essential for keeping timelines on track and ensuring all study startup activities are completed efficiently.

What is a Remote Clinical Study Startup?

A Remote Clinical Study Startup refers to the initial phase of setting up clinical trials, conducted primarily through digital tools and remote processes. This includes activities like site identification, regulatory submissions, contract negotiations, and ethics approvals, all managed without requiring in-person meetings. Remote startups leverage technology to streamline processes, reduce timelines, and improve collaboration among stakeholders. This approach is especially useful for multi-site studies or when in-person interactions are limited by geography or global events.

What is the difference between Remote Clinical Study Startup vs Remote Clinical Trial Coordinator?

AspectRemote Clinical Study StartupRemote Clinical Trial Coordinator
Primary RolePlanning and initiating clinical studies, including site selection and regulatory submissionsManaging daily trial activities, site communication, and data collection
Required CredentialsTypically a background in life sciences, clinical research certifications preferredSimilar credentials, often with clinical research or coordinator certifications
Work EnvironmentPrimarily remote, collaborating with sponsors, CROs, and sitesRemote or hybrid, focusing on site management and data oversight
Industry UsageUsed during study initiation phaseUsed during trial execution phase

Remote Clinical Study Startup involves planning and launching new clinical trials, while Remote Clinical Trial Coordinator focuses on managing ongoing trial activities. Both roles require similar credentials and often operate remotely within the clinical research industry, but they differ in their specific responsibilities and timing within the study lifecycle.

What are the most commonly searched types of Clinical Study Startup jobs in Indiana? The most popular types of Clinical Study Startup jobs in Indiana are:
What are popular job titles related to Remote Clinical Study Startup jobs in Indiana? For Remote Clinical Study Startup jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Study Startup jobs in Indiana look for? The top searched job categories for Remote Clinical Study Startup jobs in Indiana are:
What cities in Indiana are hiring for Remote Clinical Study Startup jobs? Cities in Indiana with the most Remote Clinical Study Startup job openings:
Remote Clinical Study Startup jobs near you
Infographic showing various Remote Clinical Study Startup job openings in Indiana as of May 2026, with employment types broken down into 94% Full Time, 4% Part Time, 1% Contract, and 1% Nights. Highlights an 80% Physical, 5% Hybrid, and 15% Remote job distribution.

Oncology Clinical Researcher

Alignerr

Indianapolis, IN • Remote

Full-time

Posted 9 days ago

Job description

Oncology Clinical Researcher (AI Training)
About the Role
What if your deep expertise in cancer clinical trials could directly shape how AI understands and reasons about oncology - influencing research that could one day impact millions of patients?
We're looking for experienced Oncology Clinical Researchers to bring real-world clinical rigor into cutting-edge AI development. You'll work alongside leading AI research teams to ensure that the systems being built to transform cancer research are grounded in accurate, regulatory-aligned, and scientifically sound clinical knowledge.
This is a fully remote, flexible contract role. No AI background needed - just deep oncology expertise and a sharp eye for clinical quality.
  • Organization
    : Alignerr
  • Type
    : Hourly Contract
  • Location
    : Remote
  • Commitment
    : 10-40 hours/week
    • What You'll Do
    • Review and evaluate AI-generated oncology content for clinical accuracy, scientific validity, and regulatory alignment
    • Apply your expertise in trial design - including protocol development, patient enrollment standards, and ethical compliance - to assess and improve AI outputs
    • Analyze AI-generated interpretations of cancer trial data, including safety profiles, efficacy endpoints, and biomarker findings
    • Evaluate how well AI systems translate trial outcomes into regulatory and scientific contexts relevant to FDA/EMA standards
    • Provide structured, expert feedback that directly shapes how frontier AI models reason about real oncology data
    • Work independently and asynchronously - fully on your own schedule
    Who You Are
    • Experienced in designing and managing oncology clinical trials from protocol development through data readout
    • Strong command of oncology clinical data analysis - endpoints, safety profiles, biomarkers, and beyond
    • Solid familiarity with regulatory submission standards for agencies such as the FDA or EMA
    • Naturally detail-oriented with a rigorous, systematic approach to evaluating clinical information
    • Able to communicate complex clinical findings clearly and concisely in written form
    • No prior AI or tech experience required
    Nice to Have
    • Prior experience with data annotation, data quality assessment, or AI evaluation workflows
    • Background in translational oncology, clinical pharmacology, or regulatory affairs
    • Experience authoring or reviewing clinical study reports, IND/NDA submissions, or publications
    • Familiarity with AI tools or clinical decision support platforms as an end user
    Why Join Us
    • Work directly on frontier AI systems that are transforming how cancer research is conducted
    • Fully remote and flexible - work when and where it suits you
    • Freelance autonomy with the structure of meaningful, high-impact project work
    • Influence how AI models understand, evaluate, and reason about real-world oncology data
    • Collaborate with world-leading AI research teams and labs
    • Potential for ongoing work and contract extension as new projects launch

Apply