National Clinical Research and Financial Analyst

Tenet Healthcare

Clinical research and financial analyst supporting Tenet Health clinical trials, budgets, billing, data analysis, and regulatory compliance. Preparing study reports and maintaining accurate research records.

Posted 8/11/2026full-timeRemote • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical research data analysis, financial management, and regulatory compliance, with a strong focus on data integrity and quality assurance. Proficient in collaborating with multidisciplinary teams and effectively communicating complex information to stakeholders.

Highest-signal resume keywords

Clinical Research Data AnalysisFinancial ManagementRegulatory ComplianceData Management PrinciplesMicrosoft Excel Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research MethodologiesData AnalysisBudget ProjectionsContract CreationQuality Assurance ReviewsProject ManagementFiscal PlanningStatistical AnalysisProtocol InterpretationProcess Improvement

Soft Skills

Analytical SkillsOrganizational SkillsProblem-Solving SkillsInterpersonal SkillsCommunication Skills

Tools & Technologies

Microsoft Office SuiteResearch Management SoftwareClinical Trial Management SystemsSASSPSSRPython

Certifications & Qualifications

Good Clinical Practice (GCP)HIPAA Compliance

Industry Keywords

FDA RegulationsNCI StandardsOHRP StandardsDepartment of Health and Human ServicesHuman Subject Protections

Tech Stack

Tools & technologies

Google Cloud PlatformPython

About the role

Key responsibilities & impact

Analyze clinical research data to identify trends, ensure data integrity, and support research objectives
Make financial and business decisions based on complex protocols and long-range financial projections
Assist with negotiation of clinical research budgets with industry sponsors, federal agencies, and private foundations
Provide Medicare coverage and billing analyses and implement documented billing plans for protocols
Assess the financial management structure of clinical research projects
Assist in developing, implementing, and monitoring clinical research protocols and study procedures
Maintain accurate clinical research databases and ensure completeness and quality of study data
Prepare reports, dashboards, summaries, and presentations for investigators, sponsors, and leadership
Support IRB submissions, regulatory documentation, and study compliance activities
Monitor study progress and adherence to budgets
Collaborate with physicians, investigators, research coordinators, statisticians, and multidisciplinary teams
Perform quality assurance reviews and assist with internal audits
Track study milestones, enrollment, adverse events, protocol deviations, and research metrics
Track and audit finances, including account reconciliation, reimbursements, expenditures, budget projections, invoicing, collections, and patient care costs
Maintain confidential research records and safeguard protected health information
Recommend process improvements to enhance research quality, efficiency, and compliance
Mentor, coach, train, and educate constituents on clinical research billing regulations
Perform other related duties as assigned
Occasionally work evenings or weekends to support research activities or deadlines

Requirements

What you’ll need

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
Ability to make financial/business decisions based on complex protocols and long-range financial projections
Knowledge of fiscal planning and analysis principles and practices
Knowledge of federal governance standards, including FDA, NCI, OHRP, and Department of Health and Human Services standards
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 contracts
Strong quantitative and qualitative data analysis skills
Strong analytical, organizational, problem-solving, project management, and interpersonal skills
Excellent written and verbal communication skills
Ability to manage multiple projects while meeting deadlines
Excellent attention to detail and commitment to data quality
Ability to work independently and collaboratively within multidisciplinary teams
Proficiency with Microsoft Office Suite and research management software
Strong communication skills with investigators, research staff, sponsors, and participants
Preferred: experience with clinical trial management systems such as Clinical Conductor
Preferred: knowledge of SAS, SPSS, R, or Python
Preferred: experience with grant-funded or academic research programs

Benefits

Comp & perks

🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account Tenet Healthcare Website LinkedIn All Job Openings 10,000+ employees 🏥 Healthcare 🧬 Biotechnology 🧘 Wellness 💰 $2G Post-IPO Debt on 2022-05 Healthcare
Biotechnology
Wellness Tenet Healthcare is a leading healthcare services company that owns and operates hospitals, outpatient centers, and other healthcare facilities. With a focus on providing high-quality and accessible medical care to communities across the United States, Tenet Healthcare is committed to improving patient outcomes and enhancing the healthcare experience. They also offer innovative treatment options and invest in health technology to support their mission of delivering exceptional care. National Clinical Research and Financial Analyst Job not on LinkedIn 🔥 2 minutes ago 🇺🇸 United States – Remote ⏰ Full Time 🟢 Junior 🟡 Mid-level 🧪 Clinical Research Apply Now Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
Analyze clinical research data to identify trends, ensure data integrity, and support research objectives
Make financial and business decisions based on complex protocols and long-range financial projections
Assist with negotiation of clinical research budgets with industry sponsors, federal agencies, and private foundations
Provide Medicare coverage and billing analyses and implement documented billing plans for protocols
Assess the financial management structure of clinical research projects
Assist in developing, implementing, and monitoring clinical research protocols and study procedures
Maintain accurate clinical research databases and ensure completeness and quality of study data
Prepare reports, dashboards, summaries, and presentations for investigators, sponsors, and leadership
Support IRB submissions, regulatory documentation, and study compliance activities
Monitor study progress and adherence to budgets
Collaborate with physicians, investigators, research coordinators, statisticians, and multidisciplinary teams
Perform quality assurance reviews and assist with internal audits
Track study milestones, enrollment, adverse events, protocol deviations, and research metrics
Track and audit finances, including account reconciliation, reimbursements, expenditures, budget projections, invoicing, collections, and patient care costs
Maintain confidential research records and safeguard protected health information
Recommend process improvements to enhance research quality, efficiency, and compliance
Mentor, coach, train, and educate constituents on clinical research billing regulations
Perform other related duties as assigned
Occasionally work evenings or weekends to support research activities or deadlines 🎯 Requirements
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
Ability to make financial/business decisions based on complex protocols and long-range financial projections
Knowledge of fiscal planning and analysis principles and practices
Knowledge of federal governance standards, including FDA, NCI, OHRP, and Department of Health and Human Services standards
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 contracts
Strong quantitative and qualitative data analysis skills
Strong analytical, organizational, problem-solving, project management, and interpersonal skills
Excellent written and verbal communication skills
Ability to manage multiple projects while meeting deadlines
Excellent attention to detail and commitment to data quality
Ability to work independently and collaboratively within multidisciplinary teams
Proficiency with Microsoft Office Suite and research management software
Strong communication skills with investigators, research staff, sponsors, and participants
Preferred: experience with clinical trial management systems such as Clinical Conductor
Preferred: knowledge of SAS, SPSS, R, or Python
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