Remote Financial Analyst Jobs
Remote financial analyst jobs are open across the U.S. at remote-first firms and distributed teams in sectors like fintech, SaaS, insurance, and healthcare. Employers hiring remotely right now include Emory University, CareFirst BlueCross BlueShield, and Alpaca. Scan the live roles below and apply to whichever ones fit.
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Job Summary
The Clinical Research & Financial Analyst provides analytical, operational, financial and regulatory support for clinical research studies and programs at Tenet Health. This position assists investigators and research teams in the planning, implementation, monitoring, contracting, and reporting of clinical research activities while ensuring compliance with federal regulations, institutional policies, and study protocols. This position analyzes clinical and research data, prepares reports, supports regulatory submissions, and contributes to the successful execution of clinical trials and observational research.
Responsibilities
- Analyze clinical research data to identify trends, ensure data integrity, and support research objectives.
- Ability to make financial/business decisions based on complex protocols and long-range financial projections. Knowledge on applications of principles and practices of fiscal planning and analysis.
- Assist with negotiation of clinical research budgets with industry sponsors, federal agencies, and private foundations. Responsibilities include providing a Medicare coverage analysis and billing analysis based on a review of the study protocol, contract, budget, and informed consent form (as it relates to payment of study expenses), and implementing a Documented Billing Plan for each protocol.
- Responsible for assessing the structure of financial management of clinical research projects.
- Knowledge of Federal standards of governance, including the FDA, NCI, OHRP and broader Department of Health and Human Services standards as may apply to clinical practice with investigational agents and research with human subjects.
- Assist in the development, implementation, and monitoring of clinical research protocols and study procedures.
- Maintain accurate clinical research databases and ensure completeness and quality of study data specific to clinical trial management software.
- Prepare reports, dashboards, summaries, and presentations for investigators, sponsors, and leadership.
- Support Institutional Review Board (IRB) submissions, regulatory documentation, and study compliance activities.
- Monitor study progress to ensure adherence to budgets
- Collaborate with physicians, investigators, research coordinators, statisticians, and other multidisciplinary team members.
- Perform quality assurance reviews and assist with internal audits to ensure compliance with Good Clinical Practice (GCP), FDA regulations, HIPAA, and institutional policies.
- Track study milestones, enrollment, adverse events, protocol deviations, and research metrics.
- Financial tracking and audits of the accounts including: Reconciliation of accounts, reimbursements and expenditures, accuracy of budget projections, timeliness of payment invoicing and collection, creating financial and retrospective reporting; analyzing patient care costs billed to study or insurance. Implement detail billing payment to track expenditures, payments milestone payments, monthly Quarterly billing of translation invoices to Sponsors or internal departments as well as collections.
- Maintain confidential research records and safeguard protected health information.
- Recommend process improvements that enhance research quality, efficiency, and compliance.
- Mentor, coach, train and educate, as appropriate all advocate constituents to ensure strict compliance with clinical research billing regulations. Responsible for assuring the financial compliance of the program as stipulated by the study sponsor, federal, state, and local agencies.
- Perform other related duties as assigned.
- Occasional evening or weekend work may be required to support research activities or study deadlines.
Qualifications
Minimum
- Bachelor's degree
- Two (2) years of experience supporting clinical research, healthcare analytics, regulatory compliance, or research administration.
- Experience working with research databases and Microsoft Office applications, particularly Excel.
- Knowledge of clinical research methodologies, data management principles, and regulatory requirements.
- Strong analytical, organizational, and problem-solving skills.
- Ability to make financial/business decisions based on complex protocols and long-range financial projections. Knowledge on applications of principles and practices of fiscal planning and analysis.
- Knowledge of Federal standards of governance, including the FDA, NCI, OHRP and broader Department of Health and Human Services standards as may apply to clinical practice with investigational agents and research with human subjects.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects while meeting deadlines.
- Knowledge of Good Clinical Practice (GCP), FDA regulations, HIPAA, and human subject protections.
- Ability to interpret clinical protocols, research regulations, and technical documentation.
- Ability to analyze financial data and protocols and create subsequent contracts.
- Strong quantitative and qualitative data analysis skills.
- Excellent attention to detail and commitment to data quality.
- Ability to work independently and collaboratively within multidisciplinary teams.
- Effective project management and organizational skills.
- Proficiency with Microsoft Office Suite and research management software.
- Strong interpersonal skills and the ability to communicate effectively with investigators, research staff, sponsors, and participants.
Preferred
- Experience with clinical trial management systems (e.g. Clinical Conductor).
- Knowledge of statistical software such as SAS, SPSS, R, or Python.
- Experience with grant-funded or academic research programs.
#LI-BO1
Employment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.
Tenet participates in the E-Verify program. Follow the link below for additional information.
E-Verify: http://www.uscis.gov/e-verify
The employment practices of Tenet Healthcare and its companies comply with all applicable laws and regulations.
- Analyze clinical research data to identify trends, ensure data integrity, and support research objectives.
- Ability to make financial/business decisions based on complex protocols and long-range financial projections. Knowledge on applications of principles and practices of fiscal planning and analysis.
- Assist with negotiation of clinical research budgets with industry sponsors, federal agencies, and private foundations. Responsibilities include providing a Medicare coverage analysis and billing analysis based on a review of the study protocol, contract, budget, and informed consent form (as it relates to payment of study expenses), and implementing a Documented Billing Plan for each protocol.
- Responsible for assessing the structure of financial management of clinical research projects.
- Knowledge of Federal standards of governance, including the FDA, NCI, OHRP and broader Department of Health and Human Services standards as may apply to clinical practice with investigational agents and research with human subjects.
- Assist in the development, implementation, and monitoring of clinical research protocols and study procedures.
- Maintain accurate clinical research databases and ensure completeness and quality of study data specific to clinical trial management software.
- Prepare reports, dashboards, summaries, and presentations for investigators, sponsors, and leadership.
- Support Institutional Review Board (IRB) submissions, regulatory documentation, and study compliance activities.
- Monitor study progress to ensure adherence to budgets
- Collaborate with physicians, investigators, research coordinators, statisticians, and other multidisciplinary team members.
- Perform quality assurance reviews and assist with internal audits to ensure compliance with Good Clinical Practice (GCP), FDA regulations, HIPAA, and institutional policies.
- Track study milestones, enrollment, adverse events, protocol deviations, and research metrics.
- Financial tracking and audits of the accounts including: Reconciliation of accounts, reimbursements and expenditures, accuracy of budget projections, timeliness of payment invoicing and collection, creating financial and retrospective reporting; analyzing patient care costs billed to study or insurance. Implement detail billing payment to track expenditures, payments milestone payments, monthly Quarterly billing of translation invoices to Sponsors or internal departments as well as collections.
- Maintain confidential research records and safeguard protected health information.
- Recommend process improvements that enhance research quality, efficiency, and compliance.
- Mentor, coach, train and educate, as appropriate all advocate constituents to ensure strict compliance with clinical research billing regulations. Responsible for assuring the financial compliance of the program as stipulated by the study sponsor, federal, state, and local agencies.
- Perform other related duties as assigned.
- Occasional evening or weekend work may be required to support research activities or study deadlines.
Minimum
- Bachelor's degree
- Two (2) years of experience supporting clinical research, healthcare analytics, regulatory compliance, or research administration.
- Experience working with research databases and Microsoft Office applications, particularly Excel.
- Knowledge of clinical research methodologies, data management principles, and regulatory requirements.
- Strong analytical, organizational, and problem-solving skills.
- Ability to make financial/business decisions based on complex protocols and long-range financial projections. Knowledge on applications of principles and practices of fiscal planning and analysis.
- Knowledge of Federal standards of governance, including the FDA, NCI, OHRP and broader Department of Health and Human Services standards as may apply to clinical practice with investigational agents and research with human subjects.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects while meeting deadlines.
- Knowledge of Good Clinical Practice (GCP), FDA regulations, HIPAA, and human subject protections.
- Ability to interpret clinical protocols, research regulations, and technical documentation.
- Ability to analyze financial data and protocols and create subsequent contracts.
- Strong quantitative and qualitative data analysis skills.
- Excellent attention to detail and commitment to data quality.
- Ability to work independently and collaboratively within multidisciplinary teams.
- Effective project management and organizational skills.
- Proficiency with Microsoft Office Suite and research management software.
- Strong interpersonal skills and the ability to communicate effectively with investigators, research staff, sponsors, and participants.
Preferred
- Experience with clinical trial management systems (e.g. Clinical Conductor).
- Knowledge of statistical software such as SAS, SPSS, R, or Python.
- Experience with grant-funded or academic research programs.
#LI-BO1
Job Summary
The Clinical Research & Financial Analyst provides analytical, operational, financial and regulatory support for clinical research studies and programs at Tenet Health. This position assists investigators and research teams in the planning, implementation, monitoring, contracting, and reporting of clinical research activities while ensuring compliance with federal regulations, institutional policies, and study protocols. This position analyzes clinical and research data, prepares reports, supports regulatory submissions, and contributes to the successful execution of clinical trials and observational research.
Responsibilities
- Analyze clinical research data to identify trends, ensure data integrity, and support research objectives.
- Ability to make financial/business decisions based on complex protocols and long-range financial projections. Knowledge on applications of principles and practices of fiscal planning and analysis.
- Assist with negotiation of clinical research budgets with industry sponsors, federal agencies, and private foundations. Responsibilities include providing a Medicare coverage analysis and billing analysis based on a review of the study protocol, contract, budget, and informed consent form (as it relates to payment of study expenses), and implementing a Documented Billing Plan for each protocol.
- Responsible for assessing the structure of financial management of clinical research projects.
- Knowledge of Federal standards of governance, including the FDA, NCI, OHRP and broader Department of Health and Human Services standards as may apply to clinical practice with investigational agents and research with human subjects.
- Assist in the development, implementation, and monitoring of clinical research protocols and study procedures.
- Maintain accurate clinical research databases and ensure completeness and quality of study data specific to clinical trial management software.
- Prepare reports, dashboards, summaries, and presentations for investigators, sponsors, and leadership.
- Support Institutional Review Board (IRB) submissions, regulatory documentation, and study compliance activities.
- Monitor study progress to ensure adherence to budgets
- Collaborate with physicians, investigators, research coordinators, statisticians, and other multidisciplinary team members.
- Perform quality assurance reviews and assist with internal audits to ensure compliance with Good Clinical Practice (GCP), FDA regulations, HIPAA, and institutional policies.
- Track study milestones, enrollment, adverse events, protocol deviations, and research metrics.
- Financial tracking and audits of the accounts including: Reconciliation of accounts, reimbursements and expenditures, accuracy of budget projections, timeliness of payment invoicing and collection, creating financial and retrospective reporting; analyzing patient care costs billed to study or insurance. Implement detail billing payment to track expenditures, payments milestone payments, monthly Quarterly billing of translation invoices to Sponsors or internal departments as well as collections.
- Maintain confidential research records and safeguard protected health information.
- Recommend process improvements that enhance research quality, efficiency, and compliance.
- Mentor, coach, train and educate, as appropriate all advocate constituents to ensure strict compliance with clinical research billing regulations. Responsible for assuring the financial compliance of the program as stipulated by the study sponsor, federal, state, and local agencies.
- Perform other related duties as assigned.
- Occasional evening or weekend work may be required to support research activities or study deadlines.
Qualifications
Minimum
- Bachelor's degree
- Two (2) years of experience supporting clinical research, healthcare analytics, regulatory compliance, or research administration.
- Experience working with research databases and Microsoft Office applications, particularly Excel.
- Knowledge of clinical research methodologies, data management principles, and regulatory requirements.
- Strong analytical, organizational, and problem-solving skills.
- Ability to make financial/business decisions based on complex protocols and long-range financial projections. Knowledge on applications of principles and practices of fiscal planning and analysis.
- Knowledge of Federal standards of governance, including the FDA, NCI, OHRP and broader Department of Health and Human Services standards as may apply to clinical practice with investigational agents and research with human subjects.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects while meeting deadlines.
- Knowledge of Good Clinical Practice (GCP), FDA regulations, HIPAA, and human subject protections.
- Ability to interpret clinical protocols, research regulations, and technical documentation.
- Ability to analyze financial data and protocols and create subsequent contracts.
- Strong quantitative and qualitative data analysis skills.
- Excellent attention to detail and commitment to data quality.
- Ability to work independently and collaboratively within multidisciplinary teams.
- Effective project management and organizational skills.
- Proficiency with Microsoft Office Suite and research management software.
- Strong interpersonal skills and the ability to communicate effectively with investigators, research staff, sponsors, and participants.
Preferred
- Experience with clinical trial management systems (e.g. Clinical Conductor).
- Knowledge of statistical software such as SAS, SPSS, R, or Python.
- Experience with grant-funded or academic research programs.
#LI-BO1
Employment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.
Tenet participates in the E-Verify program. Follow the link below for additional information.
E-Verify: http://www.uscis.gov/e-verify
The employment practices of Tenet Healthcare and its companies comply with all applicable laws and regulations.
- Analyze clinical research data to identify trends, ensure data integrity, and support research objectives.
- Ability to make financial/business decisions based on complex protocols and long-range financial projections. Knowledge on applications of principles and practices of fiscal planning and analysis.
- Assist with negotiation of clinical research budgets with industry sponsors, federal agencies, and private foundations. Responsibilities include providing a Medicare coverage analysis and billing analysis based on a review of the study protocol, contract, budget, and informed consent form (as it relates to payment of study expenses), and implementing a Documented Billing Plan for each protocol.
- Responsible for assessing the structure of financial management of clinical research projects.
- Knowledge of Federal standards of governance, including the FDA, NCI, OHRP and broader Department of Health and Human Services standards as may apply to clinical practice with investigational agents and research with human subjects.
- Assist in the development, implementation, and monitoring of clinical research protocols and study procedures.
- Maintain accurate clinical research databases and ensure completeness and quality of study data specific to clinical trial management software.
- Prepare reports, dashboards, summaries, and presentations for investigators, sponsors, and leadership.
- Support Institutional Review Board (IRB) submissions, regulatory documentation, and study compliance activities.
- Monitor study progress to ensure adherence to budgets
- Collaborate with physicians, investigators, research coordinators, statisticians, and other multidisciplinary team members.
- Perform quality assurance reviews and assist with internal audits to ensure compliance with Good Clinical Practice (GCP), FDA regulations, HIPAA, and institutional policies.
- Track study milestones, enrollment, adverse events, protocol deviations, and research metrics.
- Financial tracking and audits of the accounts including: Reconciliation of accounts, reimbursements and expenditures, accuracy of budget projections, timeliness of payment invoicing and collection, creating financial and retrospective reporting; analyzing patient care costs billed to study or insurance. Implement detail billing payment to track expenditures, payments milestone payments, monthly Quarterly billing of translation invoices to Sponsors or internal departments as well as collections.
- Maintain confidential research records and safeguard protected health information.
- Recommend process improvements that enhance research quality, efficiency, and compliance.
- Mentor, coach, train and educate, as appropriate all advocate constituents to ensure strict compliance with clinical research billing regulations. Responsible for assuring the financial compliance of the program as stipulated by the study sponsor, federal, state, and local agencies.
- Perform other related duties as assigned.
- Occasional evening or weekend work may be required to support research activities or study deadlines.
Minimum
- Bachelor's degree
- Two (2) years of experience supporting clinical research, healthcare analytics, regulatory compliance, or research administration.
- Experience working with research databases and Microsoft Office applications, particularly Excel.
- Knowledge of clinical research methodologies, data management principles, and regulatory requirements.
- Strong analytical, organizational, and problem-solving skills.
- Ability to make financial/business decisions based on complex protocols and long-range financial projections. Knowledge on applications of principles and practices of fiscal planning and analysis.
- Knowledge of Federal standards of governance, including the FDA, NCI, OHRP and broader Department of Health and Human Services standards as may apply to clinical practice with investigational agents and research with human subjects.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects while meeting deadlines.
- Knowledge of Good Clinical Practice (GCP), FDA regulations, HIPAA, and human subject protections.
- Ability to interpret clinical protocols, research regulations, and technical documentation.
- Ability to analyze financial data and protocols and create subsequent contracts.
- Strong quantitative and qualitative data analysis skills.
- Excellent attention to detail and commitment to data quality.
- Ability to work independently and collaboratively within multidisciplinary teams.
- Effective project management and organizational skills.
- Proficiency with Microsoft Office Suite and research management software.
- Strong interpersonal skills and the ability to communicate effectively with investigators, research staff, sponsors, and participants.
Preferred
- Experience with clinical trial management systems (e.g. Clinical Conductor).
- Knowledge of statistical software such as SAS, SPSS, R, or Python.
- Experience with grant-funded or academic research programs.
#LI-BO1
See All 177+ Remote Financial Analyst Jobs
Find roles that match your experience and apply in just a few clicks.
Find Remote Financial Analyst JobsRemote Financial Analyst Job Market
Who's Hiring
Top Industries Hiring
- Technology & Software
- Healthcare & Medical Services
- Insurance
- Consulting & Professional Services
- Retail
What Employers Look For
The qualifications that appear most often in remote financial analyst jobs.
- Bachelor's degree in finance, accounting, economics, or a related field
- Advanced Excel proficiency including financial modeling and scenario analysis
- Experience with financial reporting, forecasting, and variance analysis
- Familiarity with ERP systems such as SAP, Oracle, or Workday
- CFA designation or active progress toward charterholder status
- Strong communication skills for presenting findings to non-finance stakeholders
Tips for Your Remote Financial Analyst Job Search
Apply early to remote roles that fit
Migrate Mate lists remote financial analyst openings from across the U.S. in one place. Check regularly and apply to roles that match your experience as soon as they appear, since remote postings often attract high volume quickly.
Show async communication skills upfront
Remote financial analyst roles depend on written clarity. Structure your cover letter and any take-home materials the way you would a stakeholder memo, because remote employers use that writing to judge how you'll communicate analysis without a meeting.
Build a portfolio of clean financial models
Remote employers can't watch you work, so your models do the talking. Share a Google Sheets or Excel file with clear assumptions, labeled tabs, and documented logic. A forecasting model or variance analysis you built independently is concrete proof of remote-ready skills.
Prepare for remote-style interviews and assessments
Many remote financial analyst interviews include a take-home case or live model walk-through over video. Practice narrating your analytical logic aloud while screen-sharing, since explaining your reasoning clearly in that format is a core part of how remote teams evaluate candidates.
Remote Financial Analyst Jobs: Frequently Asked Questions
How do I get a remote financial analyst job?
Target companies with established distributed teams, such as remote-first fintech firms, SaaS businesses, and insurance companies, because they already have the infrastructure for remote finance work. Remote employers screen heavily for self-direction, strong written communication, and proficiency in collaborative tools like Excel, Google Sheets, and cloud-based reporting platforms. Candidates who show clean, well-documented financial models and a history of delivering analysis independently stand out.
Which companies hire remote financial analysts?
Companies hiring remote financial analysts right now include Emory University, CareFirst BlueCross BlueShield, and Alpaca, based on current remote listings on Migrate Mate as of August 2026. Remote-first firms and distributed enterprise teams in fintech, healthcare, and SaaS tend to hire financial analysts remotely most consistently.
Can you get a remote financial analyst job with no experience?
Yes, but remote entry-level financial analyst roles are harder to land because employers expect you to work independently from day one with minimal hand-holding. Startups and smaller remote-first companies are the most likely to hire entry-level candidates. A portfolio of financial models, a personal budgeting or forecasting project, or a relevant certification like CFA Level I can substitute for direct work history.
Do you need a degree for remote financial analyst jobs?
Usually, but not always. Most remote financial analyst postings list a bachelor's degree in finance, accounting, or economics as a baseline requirement. Remote employers do weigh demonstrated skills heavily, though, so candidates who can show polished financial models, proficiency in Excel or SQL, and real analytical outputs sometimes move forward without a traditional four-year degree.
Which industries hire the most remote financial analysts?
Remote financial analyst roles concentrate in Technology & Software, Healthcare & Medical Services, and Insurance, based on current remote listings on Migrate Mate as of August 2026. These sectors tend to have distributed finance teams that rely on cloud-based reporting and async workflows, making remote financial analyst roles a natural fit.
See All 177+ Remote Financial Analyst Jobs
Find roles that match your experience and apply in just a few clicks.
Find Remote Financial Analyst Jobs