National Clinical Research and Financial Analyst

🕒 August 11

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Tenet Healthcare

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

👥 B2C

💰 $2G Post IPO debt on 2022-07

Healthcare • B2C

Tenet Healthcare is a for-profit healthcare services company that owns and/or operates hospitals and hospital programs through subsidiaries and affiliates across the United States. The company's website and materials describe acute-care hospitals, emergency centers, specialty services (including cancer centers and advanced cardiac imaging), medical office buildings, physician careers and community health networks; Tenet emphasizes compliance, community service, and clinical innovation.

📋 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 • Preferred: experience with grant-funded or academic research programs