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Remote Clinical Study Startup Jobs (NOW HIRING)

Danaher

Senior Clinical Study Manager

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU ... will be a remote role. In this role, you will have the opportunity to: * Provide strategic ...

Danaher

Senior Clinical Study Manager

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU ... will be a remote role. In this role, you will have the opportunity to: * Provide strategic ...

NAMSA

Clinical Study Manager

$115K/yr

... on-site or remote training, follow-up, activation) oProvides site training, when necessary ... etc.) oDevelops clinical study report General project compliance: ensures that adherence to ...

ICON

Country Study Operations Manager

Blue Bell, PA · On-site

Country Study Operations Manager- Remote ICON is a global healthcare intelligence and clinical ... Provides country level input on Startup and Recruitment milestones as provided by pCRO and/or ...

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How much do remote clinical study startup jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for remote clinical study startup in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

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 are the key skills and qualifications needed to thrive as a remote clinical study startup specialist?

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 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.

More about Remote Clinical Study Startup jobs

What cities are hiring for Remote Clinical Study Startup jobs?

Cities with the most Remote Clinical Study Startup job openings:

What are the most commonly searched types of Clinical Study Startup jobs?

The most popular types of Clinical Study Startup jobs are:

What states have the most Remote Clinical Study Startup jobs?

States with the most job openings for Remote Clinical Study Startup jobs include:

What job categories do people searching Remote Clinical Study Startup jobs look for?

The top searched job categories for Remote Clinical Study Startup jobs are:

Remote Clinical Study Startup jobs near you
Infographic showing various Remote Clinical Study Startup job openings in the United States 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, with an average salary of $130,034 per year, or $62.5 per hour.

Senior Clinical Study Manager (CSM)

System One

Cleveland, OH • Remote

$60 - $80/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 6 days ago

Job description

Job Title: Senior Clinical Study Manager (CSM) Location: 100% Remote Type: Contract - 6 months with desire to go permanent Compensation: $60.00 - $80.00 Work Model: Remote – offsite

Joule is current looking to hire aSenior Clinical Study Manager (CSM) to support clinical programs focused on cell/gene therapy and oncology for one of our clients. This is a remote, 40-hour/week contract (initial ~6 months) with the potential to renew or convert to full-time based on project need, performance, and budget. In this role, you will lead day-to-day study execution by partnering with CROs, sites, and cross-functional stakeholders while ensuring compliance with ICH-GCP and FDA requirements. The ideal candidate brings 8–10 years of clinical operations experience (including 4–5+ years in study management within pharma/biotech) and is comfortable managing timelines, budgets, vendors, and TMF oversight in a fast-paced environment.

Responsibilities

  • Manage and oversee clinical study activities to ensure compliance with GCP, ICH, and FDA regulations
  • Coordinate with CROs, vendors, and site teams to ensure timely progress of clinical trials
  • Prepare and review study documentation, reports, and progress updates
  • Handle budgets, contracts, and invoices related to clinical studies
  • Ensure TMF management and oversight in accordance with regulatory standards
  • Monitor site activities and ensure site management best practices

Requirements

  • University/college degree (BS/BA/MS) or certification in a related health profession from an appropriately accredited institution
  • 8 – 10 years’ experience, including 4 – 5 years of experience in a pharmaceutical setting
  • Previous study management experience with at least 4 – 5 years of relevant experience
  • Experience in Cell/Gene Therapy and Rare diseases; recent Oncology experience is desirable

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#LI-EL1 Ref: #568-Clinical

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About System One

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System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US

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