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Remote Clinical Research Instructor Jobs (NOW HIRING)

This is a remote position. Position Overview We are seeking a motivated and detail-oriented Clinical Research Assistant to join our growing clinical operations team. In this role, you will support ...

Remote Duration: Direct Hire FTE Must Have's: * Bachelor's Degree in Health Information Management ... Clinical Research * Clinical Informatics * Information Technology and/or Academic Healthcare ...

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 ...

This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...

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Remote Clinical Research Instructor information

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$11K

$123.8K

$190.5K

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

As of Aug 8, 2026, the average yearly pay for remote clinical research instructor in the United States is $123,840.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,500.00 and $175,000.00 per year, depending on experience, location, and employer.

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

AspectRemote Clinical Research InstructorRemote Clinical Research Coordinator
CredentialsTypically requires a clinical research certification and teaching experienceRequires clinical research certification and experience in study coordination
Work EnvironmentPrimarily online teaching, training sessions, and curriculum developmentRemote management of clinical trials, participant coordination, and data collection
Employer & IndustryEducational institutions, training companies, pharmaceutical companiesResearch sites, pharmaceutical companies, CROs
Search & Comparison IntentUnderstanding teaching roles in clinical researchUnderstanding trial management and coordination roles

The main difference is that a Remote Clinical Research Instructor focuses on educating and training others in clinical research practices, often through online courses, while a Remote Clinical Research Coordinator manages and oversees clinical trial activities remotely. Both roles require clinical research certifications but serve different functions within the industry.

More about Remote Clinical Research Instructor jobs
What cities are hiring for Remote Clinical Research Instructor jobs? Cities with the most Remote Clinical Research Instructor job openings:
What are the most commonly searched types of Clinical Research Instructor jobs? The most popular types of Clinical Research Instructor jobs are:
What states have the most Remote Clinical Research Instructor jobs? States with the most job openings for Remote Clinical Research Instructor jobs include:
Infographic showing various Remote Clinical Research Instructor job openings in the United States as of August 2026, with employment types broken down into 66% Full Time, 17% Part Time, and 17% Contract. Highlights an 100% Remote job distribution, with an average salary of $123,840 per year, or $59.5 per hour.

Clinical Budget Lead (Remote - Clinical Research)

Bruno

Raleigh, NC โ€ข Remote

Full-time

Posted 23 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.