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Remote Clinical Research Startup Jobs (NOW HIRING)

Aptive

Clinical Research Protocol Specialist

This is a full-time (40 hours/week), 100% remote position. This position is currently funded ... Coordinate study startup activities and support compliance with protocol requirements, Standard ...

Aptive

Clinical Research Protocol Specialist

This is a full-time (40 hours/week), 100% remote position. This position is currently funded ... Coordinate study startup activities and support compliance with protocol requirements, Standard ...

UAB

CLINICAL RESEARCH REGULATORY COORDINATOR III

Tampa, FL · Remote

$55K - $89K/yr

... Clinical Research Regulatory Coordinator III. This position ensures research protocol consistency ... This position is fully remote General Responsibilities * To prepare and submit multiple levels of ...

Tilda Research

... various clinical research related tasks and requirements. Some understanding of basic medical ... We are a San Francisco based startup, backed by leading venture funds and industry leaders.

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...

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Remote Clinical Research Startup information

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$49K

$107.3K

$189K

How much do remote clinical research startup jobs pay per year?

As of Jul 26, 2026, the average yearly pay for remote clinical research startup in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Clinical Research Startup vs Remote Clinical Research Coordinator?

AspectRemote Clinical Research StartupRemote Clinical Research Coordinator
CredentialsTypically requires a degree in life sciences or related field; certifications like CCR or RAC are commonRequires a degree in health sciences, nursing, or related; certifications like CCRP are preferred
Work EnvironmentStartups often operate remotely or hybrid, focusing on innovative clinical trial solutionsPrimarily remote, coordinating clinical trial activities across sites and participants
Employer & Industry UsageFound in biotech, pharma startups, and CROs focusing on new trial methodsCommon in hospitals, research institutions, and CROs managing trial logistics

The main difference is that Remote Clinical Research Startups focus on developing new clinical trial technologies and often have a broader, innovative scope, while Remote Clinical Research Coordinators handle the day-to-day management of clinical trials, ensuring protocol adherence and data collection. Both roles require relevant certifications and work in remote or hybrid environments, but their responsibilities and industry focus differ.

More about Remote Clinical Research Startup jobs
What cities are hiring for Remote Clinical Research Startup jobs? Cities with the most Remote Clinical Research Startup job openings:
What are the most commonly searched types of Clinical Research Startup jobs? The most popular types of Clinical Research Startup jobs are:
What states have the most Remote Clinical Research Startup jobs? States with the most job openings for Remote Clinical Research Startup jobs include:
What job categories do people searching Remote Clinical Research Startup jobs look for? The top searched job categories for Remote Clinical Research Startup jobs are:
Remote Clinical Research Startup jobs near you
Infographic showing various Remote Clinical Research Startup job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Clinical Budget Lead (Remote - Clinical Research)

Clinical Budget Lead (Remote - Clinical Research)

Bruno

Raleigh, NC • Remote

Full-time

Posted 10 days ago

Job description

Budget Operations Lead – Clinical Research
Location: Remote (United States)
Employment Type: Full-Time
Our client is seeking an experienced Budget Operations Lead to support global clinical trial operations by overseeing investigator budget and payment data management. This role is responsible for ensuring the accuracy and quality of study budgets, payment-related data, and investigator payment processes while collaborating with sponsors, CROs, and internal project teams.
The ideal candidate has a strong background in clinical research finance, investigator budgets, site contracts, and global payment operations, along with exceptional analytical and quality control skills.
Key Responsibilities
  • Manage and oversee study-specific global investigator payment processes.
  • Review and quality check study template budgets and site-specific budgets.
  • Reconcile study budgets, payment schedules, contracts, amendments, protocols, and related documentation.
  • Verify budget amendments and ensure payment data is accurate and complete.
  • Prepare and maintain payment data for processing throughout the study lifecycle.
  • Import, validate, and maintain client payment data within internal systems.
  • Verify payee information and maintain accurate payment records.
  • Ensure investigator payments align with Clinical Trial Agreements, protocol amendments, and sponsor requirements.
  • Monitor study timelines and proactively meet project milestones and deadlines.
  • Maintain current study documentation and communicate updates across internal teams.
  • Build strong working relationships with sponsors, investigative sites, CROs, and internal stakeholders.
  • Support additional operational initiatives and projects as needed.
Qualifications
  • Bachelor's degree or equivalent combination of education and experience.
  • Minimum of 4 years of experience in clinical research, biopharmaceuticals, or a related healthcare environment.
  • Demonstrated experience with investigator contracts, site budgets, and clinical trial payment operations.
  • Strong understanding of protocol amendments and their impact on contracts, budgets, subject visits, and payment schedules.
  • Familiarity with Electronic Data Capture (EDC) systems and how clinical data impacts payment processing.
  • Advanced proficiency in Microsoft Excel, with strong working knowledge of Word, Outlook, and SharePoint.
  • Excellent organizational, analytical, and time management skills.
  • Exceptional attention to detail and commitment to quality.
  • Ability to learn new technology quickly and adapt to changing systems and processes.
  • Self-motivated with the ability to work independently in a remote environment.
  • Strong written and verbal communication skills with a professional client-facing approach.
  • Ability to identify errors in financial data, calculations, grammar, and documentation.
  • Working knowledge of accounting principles and budgeting is preferred.
Preferred Background
Experience supporting global clinical trials, investigator payment platforms, study budgeting, contract administration, or clinical finance operations is highly desirable.
This is an excellent opportunity to join a collaborative, mission-driven organization where your expertise will directly support the successful execution of global clinical research programs.