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Remote Clinical Study Startup Jobs in Illinois (NOW HIRING)

This is a fully remote, flexible contract role. No AI background required - just a strong command ... Experience authoring or reviewing clinical study reports, IND/NDA submissions, or peer-reviewed ...

Lead Clinical Data Manager (Remote)

Chicago, IL · Remote

$68.50K - $217.10K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

Lead Clinical Data Manager (Remote)

Chicago, IL · Remote

$68.50K - $217.10K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

... remote capacity, supporting a leading academic clinical research center in Chicago. The ideal ... Serve as a subject matter expert for Medicare coverage rules, assisting study teams in identifying ...

$160K - $200K/yr

This is a North America based remote position. What You'll Do Here * Evaluate clinical pathology ... Support Study Directors in addressing clinical pathology related data and issues with sponsors.

Consulting Statistician

Chicago, IL · On-site +1

$110.50K - $184K/yr

... clinical study design and implementation. This role advises internal and external clients on ... remote based, Canada or USA) Statistical Consulting Services * Communicates with clients and ...

Clinical Trial Liaison- US- Remote ICON is a global healthcare intelligence and clinical research ... ensure study sites have a thorough understanding of the study design and procedures so that ...

Contributing to the preparation and review of study documentation, including protocols and clinical ... MM2 #LI-Remote What ICON can offer you: Our success depends on the quality of our people. That ...

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Create, review, and maintain study documentation, such as Case Report Forms (CRFs), Data Management ...

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Create, review, and maintain study documentation, such as Case Report Forms (CRFs), Data Management ...

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Create, review, and maintain study documentation, such as Case Report Forms (CRFs), Data Management ...

... across clinical studies) is highly preferred * Strong knowledge of applicable research and ... This is a remote position open to candidates in the United States. IQVIA is a leading global ...

... across clinical studies) is highly preferred * Strong knowledge of applicable research and ... This is a remote position open to candidates in the United States. IQVIA is a leading global ...

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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 Illinois? The most popular types of Clinical Study Startup jobs in Illinois are:
What cities in Illinois are hiring for Remote Clinical Study Startup jobs? Cities in Illinois with the most Remote Clinical Study Startup job openings:
Infographic showing various Remote Clinical Study Startup job openings in Illinois as of May 2026, with employment types broken down into 86% Full Time, 9% Part Time, and 5% Contract. Highlights an 100% Remote job distribution.
Associate Director of Biostatistics (Remote)

Associate Director of Biostatistics (Remote)

Astrix Inc

Lombard, IL • On-site, Remote

$170K - $215K/yr

Full-time

Posted 19 days ago


Job description

Pay Rate Low: 170000 | Pay Rate High: 210000
Our client is a growing contract research organization seeking an Associate Director, Biostatistics to provide scientific leadership and people management across multiple clinical studies! They focus on collaborative, growth oriented culture & offers competitive compensation and benefits!
Title: Associate Director, Biostatistics (Remote)
Location: Remote - United States
Salary: $170k - $215k+(Depends on experience)
Position Overview
Excellent leadership role supporting impactful clinical research programs! This fully remote role serves as a first-line manager with accountability for statistical quality, project execution, and team development in support of clinical development programs.
Key Responsibilities
  • Lead and manage a team of statisticians, ensuring high-quality statistical deliverables and on-time study execution
  • Oversee statistical resourcing across multiple clinical trials
  • Provide strategic and scientific input to clinical development programs
  • Author, review, and approve protocols, Statistical Analysis Plans (SAPs), and table shells
  • Collaborate cross-functionally with Programming, Data Management, and Clinical Operations
  • Contribute to clinical study reports, regulatory submissions, and data presentations

Qualifications
  • MS in Biostatistics, Statistics, Mathematics, or related field
  • Minimum 7 years of clinical trials experience with a Master's degree, or 5 years with a PhD
  • Strong proficiency in SAS and/or R
  • Solid understanding of statistical methods used in pharmaceutical and clinical research
  • Excellent communication and stakeholder-facing skills
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