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Full Time Remote Clinical Research Jobs (NOW HIRING)

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... fulltime #LI-remote We may use artificial intelligence (AI) tools to support parts of the hiring ...

Zeiders Enterprises

Remote Clinical Counselor

$60K - $80K/yr

Monday - Friday, 7:00am - 4:00pm Japan Standard Time / Sunday - Thursday, 6:00pm - 3:00am Eastern Time Summary The Remote Clinical Counselor works as a full-time employee of Zeiders Enterprises and ...

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Full Time Remote Clinical Research information

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$49K

$107.3K

$189K

How much do full time remote clinical research jobs pay per year?

As of Aug 4, 2026, the average yearly pay for full time remote clinical research 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.

How do remote clinical research professionals typically collaborate with on-site teams and study sponsors?

Remote clinical research professionals often use a combination of digital communication tools such as video conferencing, project management platforms, and secure data-sharing systems to stay connected with on-site teams and sponsors. Regular virtual meetings help ensure alignment on study protocols, timelines, and regulatory requirements. While most tasks can be handled remotely, strong organizational and communication skills are essential for managing documentation, resolving queries, and maintaining study integrity. Successful remote collaboration relies on proactive engagement and clear, consistent reporting to all stakeholders.

What are the key skills and qualifications needed to thrive as a full time remote clinical research professional?

To excel in a Full Time Remote Clinical Research role, you need a solid background in life sciences or healthcare, experience with clinical trials, and typically a relevant degree such as a BSN, RN, or equivalent. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like GCP (Good Clinical Practice) are commonly required. Exceptional attention to detail, strong communication skills, and self-motivation are vital soft skills for remote coordination and data integrity. These competencies ensure accurate trial management, regulatory compliance, and effective collaboration in a remote environment.

What is a full time remote clinical research job?

A Full Time Remote Clinical Research job involves conducting, managing, or supporting clinical studies from a remote location, rather than working on-site at a hospital or research facility. Professionals in these roles may be responsible for tasks such as collecting and analyzing data, monitoring clinical trials, ensuring regulatory compliance, and communicating with study participants or teams virtually. This type of role allows for greater flexibility and the ability to work from anywhere with a reliable internet connection. Candidates typically need a background in life sciences or healthcare, strong organizational skills, and proficiency with digital communication and data management tools.

What is the difference between Full Time Remote Clinical Research vs Full Time Remote Clinical Data Coordinator?

AspectFull Time Remote Clinical ResearchFull Time Remote Clinical Data Coordinator
CredentialsTypically requires a degree in life sciences, healthcare, or related field; certifications like CCR or CCRA are commonRequires a degree in health informatics, data management, or related field; certifications like CDMP may be preferred
Work EnvironmentRemote, often involves collaboration with research teams, sponsors, and sitesRemote, focused on data entry, validation, and management within clinical trials
Industry UsageCommon in pharmaceutical, biotech, and CRO industriesPrimarily in clinical trial data management within similar industries

Full Time Remote Clinical Research roles involve overseeing clinical trial processes, ensuring compliance, and coordinating with multiple stakeholders. In contrast, Full Time Remote Clinical Data Coordinators focus on managing and validating trial data. Both roles are remote and industry-related but differ in responsibilities and required credentials.

More about Full Time Remote Clinical Research jobs
What cities are hiring for Full Time Remote Clinical Research jobs? Cities with the most Full Time Remote Clinical Research job openings:
What are the most commonly searched types of Remote Clinical Research jobs? The most popular types of Remote Clinical Research jobs are:
What states have the most Full Time Remote Clinical Research jobs? States with the most job openings for Full Time Remote Clinical Research jobs include:
What job categories do people searching Full Time Remote Clinical Research jobs look for? The top searched job categories for Full Time Remote Clinical Research jobs are:
Full Time Remote Clinical Research jobs near you
Infographic showing various Full Time Remote Clinical Research 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)

Bruno

Raleigh, NC • Remote

Full-time

Posted 19 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.