National Clinical Research and Financial Analyst

This is a fully remote position, open to applicants in United States.

📋 Description

• Evaluate clinical research data to uncover trends, ensure data integrity, and support research goals.

• Make informed financial and business decisions based on intricate protocols and extensive financial forecasts.

• Aid in the negotiation of clinical research budgets with industry sponsors, federal entities, and private foundations.

• Conduct analyses of Medicare coverage and billing, implementing documented billing strategies for protocols.

• Review the financial management framework of clinical research initiatives.

• Assist in the creation, execution, and oversight of clinical research protocols and study methods.

• Maintain precise clinical research databases, ensuring the completeness and quality of study data.

• Generate reports, dashboards, summaries, and presentations for investigators, sponsors, and leadership teams.

• Support IRB submissions, regulatory documentation, and compliance activities related to studies.

• Monitor the progress of studies and adherence to budget constraints.

• Collaborate with physicians, investigators, research coordinators, statisticians, and multidisciplinary teams.

• Conduct quality assurance reviews and assist with internal audits.

• Track study milestones, participant enrollment, adverse events, protocol deviations, and research metrics.

• Manage and audit finances, including account reconciliation, reimbursements, expenditures, budget forecasts, invoicing, collections, and patient care costs.

• Safeguard confidential research records and protected health information.

• Suggest process enhancements to improve research quality, efficiency, and compliance.

• Mentor, coach, train, and educate stakeholders on clinical research billing regulations.

• Perform additional related tasks as assigned.

• Occasionally work evenings or weekends to assist with research activities or meet deadlines.

⛳️ Requirements

• A Bachelor's degree.

• Two (2) years of experience in supporting clinical research, healthcare analytics, regulatory compliance, or research administration.

• Proficiency with research databases and Microsoft Office applications, particularly Excel.

• Understanding of clinical research methodologies, data management principles, and regulatory standards.

• Capability to make financial/business decisions grounded in complex protocols and long-term financial projections.

• Familiarity with fiscal planning and analysis principles and practices.

• Knowledge of federal governance standards, including FDA, NCI, OHRP, and Department of Health and Human Services standards.

• Awareness of Good Clinical Practice (GCP), FDA regulations, HIPAA, and human subject protections.

• Ability to interpret clinical protocols, research regulations, and technical documentation.

• Proficient in analyzing financial data and protocols and creating contracts.

• Strong quantitative and qualitative data analysis capabilities.

• Excellent analytical, organizational, problem-solving, project management, and interpersonal skills.

• Outstanding written and verbal communication abilities.

• Competence in managing multiple projects while adhering to deadlines.

• Exceptional attention to detail and a commitment to data quality.

• Ability to work both independently and collaboratively within multidisciplinary teams.

• Proficiency in the Microsoft Office Suite and research management software.

• Strong communication skills with investigators, research personnel, 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

• Comprehensive health and wellness benefits.

• Opportunities for professional development and training.

• Flexible work schedule.

• Collaborative and supportive work environment.

• Potential for career advancement.