National Clinical Research and Financial Analyst

Job not on LinkedIn

🔥 0 minutes ago

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Tenet Healthcare

WebsiteLinkedInAll 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.

📋 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