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Remote Clinical Research Instructor Jobs in Raleigh, NC

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Senior Clinical Research Associate

Cary, NC · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

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Senior Clinical Research Associate

Cary, NC · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

IQVIA

Director, Remote Research Clinicians

Durham, NC · Remote

Drive advancement of technology-enabled clinical trial solutions, including workflow automation ... Remote Research Clinicians organization while allowing delivery and line management leaders to ...

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All JobsClinical Research Instructor JobsRemote Clinical Research Instructor JobsRemote Clinical Research Instructor Jobs in Raleigh, NC

Remote Clinical Research Instructor information

See Raleigh, NC salary details

$10.7K

$120.4K

$185.2K

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

As of Jul 26, 2026, the average yearly pay for remote clinical research instructor in Raleigh, NC is $120,383.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,500.00 and $170,100.00 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.

What are popular job titles related to Remote Clinical Research Instructor jobs in Raleigh, NC? For Remote Clinical Research Instructor jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Research Instructor jobs in Raleigh, NC look for? The top searched job categories for Remote Clinical Research Instructor jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Clinical Research Instructor jobs? Cities near Raleigh, NC with the most Remote Clinical Research Instructor job openings:
Remote Clinical Research Instructor jobs near you
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.