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Flexible Remote Clinical Research Jobs (NOW HIRING)

WEP Clinical

Senior Clinical Research Associate

They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ... flexible, fit-for-purpose solutions that support drug development, improve access, and help ...

Trice Healthcare

Clinical Research Informatician

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 ...

Pharmacy Careers

Remote Clinical Review Pharmacist

$121K - $144K/yr

Remote Clinical Review Pharmacist - Work From Home | Evidence-Based Decisions | Flexible Schedule Leverage your clinical knowledge in a fully remote Clinical Review Pharmacist role. Evaluate ...

New

Pharmacy Careers

Remote Clinical Review Pharmacist

$121K - $144K/yr

Remote Clinical Review Pharmacist - Work From Home | Evidence-Based Decisions | Flexible Schedule Leverage your clinical knowledge in a fully remote Clinical Review Pharmacist role. Evaluate ...

New

Pharmacy Careers

Remote Clinical Review Pharmacist

$121K - $144K/yr

Remote Clinical Review Pharmacist - Work From Home | Evidence-Based Decisions | Flexible Schedule Leverage your clinical knowledge in a fully remote Clinical Review Pharmacist role. Evaluate ...

New

Pharmacy Careers

Remote Clinical Review Pharmacist

$121K - $144K/yr

Remote Clinical Review Pharmacist - Work From Home | Evidence-Based Decisions | Flexible Schedule Leverage your clinical knowledge in a fully remote Clinical Review Pharmacist role. Evaluate ...

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Flexible Remote Clinical Research information

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$49K

$107.3K

$189K

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

As of Aug 11, 2026, the average yearly pay for flexible 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.

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

AspectFlexible Remote Clinical ResearchRemote Clinical Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, with certifications like CCR or RAC beneficialRequires a degree in health sciences, nursing, or related field; certifications like CDMP or RDC may be preferred
Work EnvironmentRemote, flexible hours, often involves collaboration with research teams and sponsorsRemote, focused on data entry, management, and quality control within clinical trials
Industry UsageCommon in pharmaceutical, biotech, and clinical research organizationsUsed mainly in clinical trial data management across similar industries

Flexible Remote Clinical Research involves broader responsibilities in managing and coordinating clinical trials remotely, while Remote Clinical Data Coordinators focus specifically on data management tasks. Both roles are remote, require relevant healthcare or science credentials, and are integral to clinical research processes.

What cities are hiring for Flexible Remote Clinical Research jobs? Cities with the most Flexible 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 Flexible Remote Clinical Research jobs? States with the most job openings for Flexible Remote Clinical Research jobs include:
Flexible Remote Clinical Research jobs near you

Clinical Budget Lead (Remote - Clinical Research)

Bruno

Raleigh, NC • Remote

Full-time

Posted 27 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.