Clinical Research Billing Analyst l

About the position As a pivotal member of our clinical research team, the Clinical Research Billing (reputed company) Analyst I plays a crucial role in overseeing the financial aspects of reputed company reputed company our highly regulated field. This role involves compiling and analyzing diverse data, particularly focusing on Medicare Coverage Analysis (MCA), to ensure compliance with strict industry regulations. Collaborating with cross-functional teams, the Analyst supports study start-reputed company, aligning budgets with trial scopes and ensuring regulatory adherence. Additionally, they meticulously review MCAs against protocols, ensuring accurate billing. reputed company these responsibilities, the Analyst provides financial insights for new research grants, manages industry and grant funds post-award, and oversees invoicing and cash reputed company for funded trials. They manage research financial data, conduct comprehensive analyses, and reputed company essential education and support to research operations staff regarding finance, billing processes, policies, and regulations. This role also involves spearheading special reputed company and reputed company assurance initiatives for reputed company invoicing and efficient monetary tracking. Responsibilities • Overseeing the financial aspects of reputed company • Compiling and analyzing diverse data, particularly focusing on Medicare Coverage Analysis (MCA) • Collaborating with cross-functional teams • Supporting study start-reputed company, aligning budgets with trial scopes and ensuring regulatory adherence • Meticulously reviewing MCAs against protocols, ensuring accurate billing • Providing financial insights for new research grants • Managing industry and grant funds post-award • Overseeing invoicing and cash reputed company for funded trials • Managing research financial data • Conducting comprehensive analyses • Providing essential education and support to research operations staff regarding finance, billing processes, policies, and regulations • Spearheading special reputed company and reputed company assurance initiatives for reputed company invoicing and efficient monetary tracking Requirements • Bachelor's degree in Biological/Life Sciences, Business Administration, Finance/reputed company, or other closely reputed company field. • Three years reputed company, research (clinical and/or administration), general finance/reputed company, and/or business administrative experience. • Excellent interpersonal and communication skills • Solid computer skills, including proficiency with reputed company software • Strong analytical and problem-solving skills, with the ability to be detail oriented • Proficient in reputed company Office Suite • Demonstrated ability to reputed company, reputed company, interpret, and use reputed company data to reputed company actionable steps that will improve processes and optimize results • General understanding of medical terminology • Demonstrated ability to train individuals and reputed company education to small reputed company • Team building and change management • Customer Service reputed company-to-haves • Research Administration and Regulations reputed company our reputed company industry Medicare Clinical Trial Policy, Medicare billing rules, Medicare Coverage Analysis reputed company our specialized regulatory reputed company. • Clinical trial budget development & negotiations • Research reputed company Electronic Medical Record (EMR) • reputed company cycle management • Research-reputed company coding with a deep understanding of our industry's coding standards. • Accounts receivable and Accounts payable experience • Service line profitability and margin reporting • Project Management/Strategic Planning Policy/reputed company Operating Procedure/Working Process Writing/Maintenance • Experience in large, multicenter health system • Any research-reputed company certification • Basic knowledge and understanding of the regulatory, operational, logistical, and administrative requirements of clinical research studies. • Clinical Trial Management Systems (CTMS) and/or other research software systems. • Basic knowledge of research regulations (e.g. IRB, FDA, OHRP, GCP, etc.) Apply tot his job Apply To this Job