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Flex Time Remote Clinical Research Jobs (NOW HIRING)

... work a Flex/Hybrid schedule with 2-3 days per week onsite in our Irvine, CA office . Remote ... time, within budget and in compliance with regulations and SOPs); * Plans, tracks and manages ...

... work a Flex/Hybrid schedule with 2-3 days per week onsite in our Irvine, CA office . Remote ... time, within budget and in compliance with regulations and SOPs); * Plans, tracks and manages ...

... 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 ...

They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ... time Paid maternity & paternity leave What Sets Us Apart: WEP Clinical partners with ...

Clinical Research Assistant

Duluth, MN · On-site +1

$18.69 - $27.85/hr

Experience in oncology, clinical research, academic research or similar area. Over 1 year computer ... Remote/Hybrid Option: Shift Rotation: Day Rotation (United States of America) Shift Start Time:

Clinical Research Coordinator

$24.75 - $33/hr

This is a remote US role, with a preference for candidates based in San Francisco, Boston, or San ... An Oura Ring of your own plus employee discounts for friends & family * 20 days of paid time off ...

Remote Clinical Counselor

$60K - $80K/yr

Monday - Friday, 7:00am - 4:00pm Japan Standard Time / Sunday - Thursday, 6:00pm - 3:00am Eastern ... Must be able to flex hours in times of surge or crisis. * Must be able to obtain a US passport for ...

This position is not eligible for visa 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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Flex Time Remote Clinical Research information

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$49K

$107.3K

$189K

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

As of Jul 26, 2026, the average yearly pay for flex 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.

What is the difference between Flex Time Remote Clinical Research vs Part-Time On-Site Clinical Research Coordinator?

AspectFlex Time Remote Clinical ResearchPart-Time On-Site Clinical Research Coordinator
Work EnvironmentRemote, flexible hoursOn-site, fixed hours
CredentialsTypically requires clinical research experience and certificationsSimilar credentials, often including CRC certification
Employer & IndustryPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Search & Comparison IntentFlexibility, remote work optionsOn-site responsibilities, part-time schedule

Flex Time Remote Clinical Research roles offer flexible, remote work environments requiring similar credentials as on-site coordinators. In contrast, Part-Time On-Site Clinical Research Coordinators work at research sites with fixed hours. Both roles involve managing clinical trials but differ mainly in location and scheduling flexibility.

More about Flex Time Remote Clinical Research jobs
What cities are hiring for Flex Time Remote Clinical Research jobs? Cities with the most Flex Time Remote Clinical Research job openings:
What states have the most Flex Time Remote Clinical Research jobs? States with the most job openings for Flex Time Remote Clinical Research jobs include:
Infographic showing various Flex 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)

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.