Collecting information
Organizing data
Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. MSK is dedicated to training the next generation of scientists and clinicians, who go on to pursue our mission at MSK and around the globe. Exciting Opportunity at MSK: Join our team as a Clinical Trials Nurse in our Early Drug Developement department at Memorial Sloan Kettering, We're looking for a dynamic nursing professional eager to showcase compassionate, evidence-based nursing care skills and make a meaningful impact. Participate in an individualized training/orientation program geared to guiding or reinforcing the principles of Clinical Trials Nursing practiced at MSKCC. Location: MSKCC, New York, NY, USA
This hospital is a leading provider of emergency and ambulatory care services to Nassau County. As the Pharmacy Supervisor , you will lead and manage pharmacy operations during evening hours, ensuring safe, compliant, and efficient medication distribution. Troubleshoot pharmacy technology (automation/information systems – Meditech.. Master's in Healthcare Administration, Informatics, or related field.. Behavioral health support, online therapy, telemedicine, and inclusive IVF benefits
Long Term Medical Billing Clerk needed for the Revenue/Billing department in Queens.. As a Medical Billing Clerk, you will play a key role in the Revenue/Billing department.. Perform data entry by transferring information from the Electronic Health Records (EHR) system to the medical billing system.. Submit insurance claims and follow up on claims processing through clearinghouses.. Monitor and resolve claim denials from Medicaid, Medicare, Managed Care, and other payers.
A Senior Regulatory Compliance Coordinator position is available within the Montefiore Einstein Cancer Center Clinical Trials Office (CCTO).. The role involves managing cancer clinical trials, ensuring regulatory compliance, developing new trials, and mentoring junior staff.. Bachelor's Degree in Science or Health Policy (required); Master's preferred.. At least 4 years of research experience in Regulatory Affairs, Clinical Affairs, or Quality Assurance.. Knowledge of Phase I-IV clinical studies, data management, GCP guidelines, and CFRs.
We are seeking a dedicated and experienced Director of Behavioral Health Quality Assurance to lead the quality improvement efforts for the Department of Psychiatry in a dynamic healthcare setting.. This key leadership role is responsible for coordinating and implementing comprehensive quality assurance, incident review, and utilization review programs across both inpatient and ambulatory care services.. Prepare and present data-driven reports to hospital leadership and regulatory bodies. Master’s degree required (in Psychology, Public Health, Healthcare Administration, or related field). CPHQ (Certified Professional in Healthcare Quality) highly desirable
Manhattan Gastroenterology is seeking an experienced and strategic health care Chief Financial Officer (CFO) to lead and oversee all financial operations across our growing network of healthcare practices.. ● Oversee accounting, billing, revenue cycle management, and compliance with healthcare regulations.. Supervise accounting operations, including general ledger, accounts payable/receivable, payroll, and fixed assets.. ● Ensures compliance with federal, state and city financial policies and regulations which includes but not limited to OMH, OASAS, ACS, NYSDOH, NYCDOH, Medicare, Medicaid, tax filings, audits and reporting requirements.. ● Strong knowledge of healthcare revenue cycle management, medical billing, and insurance reimbursement.
The Revenue Cycle Director is responsible for the day-to-day management of billing, payment posting, collections and verification/authorizations.. In addition, candidates will have in-depth knowledge of Medicare, Medicaid, Medicaid Managed Care, and Commercial Insurance billing processes particularly for NYS behavioral health services.. Clear understanding and working knowledge of claims processing, payer denials and appeals processes.. Possess intermediate computer skills, which include knowledge of word processor, spreadsheet, and database software and file maintenance.. 5 years of experience in healthcare revenue cycle management and/or medical billing processes including knowledge of ICD-10, CPT, and HCPCS codes required.
Associate Director, Regulatory Affairs - Genetic Medicine & Thrombosis. Employer: Regeneron Pharmaceuticals, Inc. | Location: Tarrytown, New York, US | Salary: Competitive | Closing date: May 10, 2025. The Associate Director of Regulatory Affairs will provide leadership on global regulatory activities for assigned products.. Join us and apply now to start your journey with Regeneron!. Regeneron is an equal opportunity employer.
Elderplan and HomeFirst, our Medicare and Medicaid managed care health plans, are outstanding examples of how we are expanding services in response to our patients' and members' needs.. Reporting to the Supervisor of Care Management this position will provide case management to our members including medical, social, psychological, physical, and spiritual needs by developing, implementing and monitoring the care plan, in conjunction with the PCP, caregivers and other team members, to help meet the member's needs.. managed care nurse, managed care rn, nursing, rn, nurse, care management. ~ CCM preferred. ~1 year of RN experience in managed care, home care, acute care or nursing home preferred
This individual will support existing products and new product introductions by providing and applying Quality Assurance and cGMP expertise for OTC drug products (monographed and NDA/ANDA).. The individual must develop and maintain an effective working relationship with QA personnel at Contractors and internal stakeholders such as Regulatory Affairs, Medical Affairs, Strategic Sourcing, New Product Development, Package Development, Supply Planning and Logistics.. Evaluates the effectiveness of Contractors’ quality systems by leading effective audits for cGMP compliance, issuing audit reports, managing Contractor response adequacy and timeliness; determining system improvements.. Prepares reports by collecting, analyzing, and summarizing regulatory and compliance data and trends such as Stability, Complaints, Nonconformance Reports, Deviations, Investigations, CAPA for Annual Product Reviews.. QUALIFICATIONS: Minimum of BS in a Scientific discipline 15 years QA experience in pharmaceutical industry (OTC preferred) with a thorough knowledge of Quality Systems, Quality Assurance, and Quality Control in a cGMP environment.
We are seeking a clinical research coordinator (CRC) for the ALS Center at Columbia University Medical Center.. The CRC will play an integral role in the coordination and conduct of clinical trials at the Center and will provide support in developing and executing ALS research initiatives.. Reporting to the Center’s Principal Investigators (PIs) and Senior Managers (SMs), the CRC will help coordinate the clinical research efforts of the ALS Center.. Assists SMs with initiation and start-up of clinical trials, including initial protocol submission, execution of contract and budget, and approvals for ancillary services (e.g. the Irving Clinical Research Center, Research Pharmacy, local laboratories, radiology). Previous experience with Epic EMR, iMedidata EDC, and/or Columbia’s RASCAL IRB module
DME Biller (Medicare Part B) – Assisted Living Experience Required. We are seeking a detail-oriented and experienced DME Biller to manage the billing and claims process for Durable Medical Equipment (DME) under Medicare Part B, specifically for residents in assisted living facilities.. Stay updated on Medicare Part B policies and changes affecting DME billing.. ~2-3 years of experience in DME billing (Medicare Part B).. ~ Strong knowledge of HCPCS codes, insurance verification, and claims processing.
Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials.. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, Sam Altman, John Doerr, Spark Capital, SV Angel Growth, and others.. Guiding in-licensing strategy, including therapeutic area focus, modality, and stage of drug development to align with Formation Bio's goals. Fostering a high-performance culture, ensuring alignment with organizational goals, and providing strategic guidance to team members in scouting, evaluating, and advancing potential opportunities. PhD preferred (in a relevant field such as biology, chemistry, pharmacology, etc.)
The Director of Biostatistics provides leadership and guidance as the statistical expert on a project team or within a therapeutic area. This position is for a qualified statistician/biostatistician to support Clinical Biostatistics within Global Development. The incumbent will lead and/or oversee the efforts of the Biostatistics department with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make decisions. Interacts with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials, as well as ensure the clinical program is appropriately designed. Knowledge of drug discovery and development and ability to integrate statistical concepts into drug discovery and development strategies.
Medical Analysts support the unit by working in partnership with its attorneys, auditors, detectives, data analysts, and legal support analysts to conduct complex, long-term healthcare fraud investigations.. Several matters that highlight MFCU’s important work include OAG’s report concerning neglect of nursing home residents across New York state during the COVID-19 pandemic, and the recent filing of four major lawsuits against nursing homes, including Centers Health Care, Cold Spring Hills Center for Nursing and Rehabilitation, The Villages of Orleans Health and Rehabilitation Center, and Fulton Commons Care Center, Inc.. Additional significant cases include securing $8.6M and significant reforms to nursing home after repeated financial fraud and resident mistreatment; the indictment and arraignment of owner of NYC pharmacy for allegedly stealing millions from Medicaid; and the sentencing of a former owner of over 20 pharmacies for running $11 Million Medicaid fraud targeting vulnerable HIV patients.. , Director of Nursing, Administrator, Risk Manager, In-Service Coordinator), including current or past employment within a long-term care facility;. Prior experience as a legal nurse consultant; and
As we have for years, we offer best-in-class programming–now across 15 sites—focusing on a mix of education, health and wellness, arts and culture, and civic engagement.. Maintain detailed receivables reports for both Part- and Part- OASAS programs and Billing Manager of any billing-related trends.. Follow up on updates and changes in pay rates, rules, and regulations pertinent to OASAS programs. Knowledge of OASAS and/or OMH/DOH regulations, APG methodology, and Value-Based Payments implementation preferred. Free Gym Membership to our Manny Cantor Center 14TH ST Y Fitness Center
The Primary Care Physician provides direct primary medical care to children and adult patients.. Works in conjunction with the chief medical officer, administrative management, practice manager, clinical nurse manager, and medical team to facilitate patient care.. Serves on health care facility committees as required (e.g., Quality Assurance, Infection Control, Complaints Committee).. Twenty- four (24) Continued Medical Education (CME) credits per credentialing cycle (two (2) years).. Knowledge of Medicare, Medicaid and third-party billing requirements preferred.
5+ years of experience in B2B sales, with a proven track record of selling into RCM organizations, healthcare billing companies, or revenue cycle teams.. Strong understanding of revenue cycle management (RCM), medical billing, coding processes, and healthcare finance operations.. A data-driven approach to sales, with proficiency in using CRM tools (e.g., Salesforce, HubSpot) to track pipeline and performance.. Familiarity with EHR systems, medical billing software, and healthcare claims processing platforms.. SuperDial is transforming AI in healthcare, focusing on revenue cycle management and operational automation for RCM organizations and healthcare providers.
Job Title : QA Associate III - On-the-floor Inspector. The purpose of the QA Associate position is to monitor and ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures (SOPs).. The Quality Assurance (QA) Associate position is an individual contributor role and a member of the InvaGen Pharmaceuticals Quality Team. The position reports to the Quality Assurance Manager and maybe matrixed to other functional leaders within the Quality or other departments.. Advanced vocational training or education in pharmaceutical manufacturing, industrial management or related field of study from an accredited college/university.is preferred.. Minimum of three (3) yearsa experience in a quality assurance in a GMP pharmaceutical manufacturing operation and work environment.
Position Summary: We have an exciting opportunity to join our team as an Assistant Director of Patient Safety.. Reporting to the Senior Director of Patient Safety/Risk Management, the successful candidate will oversee NYU Langone Health Brooklyn's Patient Safety/Risk Management staff, and develop, implement, and monitor enterprise-wide Risk Management/Patient Safety programs, projects, policies, and procedures in accordance with New York State regulations, The Joint Commission standards, and Federal requirements.. Facilitate compliance with insurance, legal, and regulatory requirements, including completion of discovery requests, insurance alerts, and adherence to New York State Department of Health and Office of Mental Health reporting requirements.. Minimum Qualifications: Registered Nurse with BSN preferred, or Bachelor's Degree in Healthcare Administration or related experience.. Deep knowledge of New York State Public Health Law, TJC standards, NYPORTS, HIPAA, and CMS Conditions of Participation.