The vision, to radically change the landscape of long-term care forever. Signature HealthCARE is a family-based healthcare company that offers integrated services in 7 states across the continuum of care: skilled nursing, rehabilitation, assisted living, memory care, home health, cognitive care, and telemedicine. Many of our skilled nursing facilities have achieved a 4 or 5-star overall rating from the Centers for Medicare & Medicaid Services. To learn more about our benefits offered, please contact Jenny Collins, Senior Director of Talent Acquisition, directly at (561) 234-0371 or jcollins@signaturehealthcarellc.com. Our culture is built on three distinct pillars: Learning, Spirituality and Intra-preneurship.
We are a small, close knit building with many long term dedicated associates, and great census!. You will supervise nursing care provided by Registered Nurses (RN), Licensed Practical Nurses (LPN) and State Tested Nursing Assistants (STNA).. - Participate in the budget process of the facility and maintains the nursing supply, equipment and nurse staffing budgets.. - Director of Nursing, management or supervisor experience in long-term care, restorative or geriatric nursing.. We are a national organization of skilled nursing, subacute, rehabilitative, and assisted living providers dedicated to achieving the highest standards of care in five states including Michigan, Ohio, Virginia, North Carolina, and Indiana.
BS degree in Accounting, Finance or Healthcare Management highly preferredThorough understanding of Generally Accepted Accounting Principles (GAAP).. Intermediate to advanced experience in MS Excel, and ability to use other MS Office products.. Intermediate to advanced knowledge of major accounting software packages for both general ledger and statutory accounting.. Healthcare billing and collection experience with nursing home receivable which includes Medicaid and Medicare Part A & B, HMO's preferred.. Experience with Medicaid Applications perferredFundamental knowledge of accounting practices and agency reimbursement programs preferred
Work Hours: Full-Time | 80 hours bi-weekly Schedule: Monday-Friday, 7:00 AM to 3:30 PM (No weekend or holiday commitment) Flexibility available based on the needs of the location.. TriHealth is seeking a mission-driven Patient Safety Consultant to join our dedicated Patient Safety team.. Advanced certification in Patient Safety, Quality, or Risk Management (e.g. CPPS, CPHQ, CPHRM, CPHFH). Provide leadership in the facilitation of TriHealth's adoption of high-reliability and other safety practices.. Pick up trash, ensuring the physical environment is clean and safe.
Graduation from an accredited program of Certified Nursing Assistant, Patient Care Technician, or Hospital Specialist AND one year experience in the medical field or completion of an approved internship program OR equivalent combination of education and experience.. Proficiency in using electronic health records (EHR) systems.. Participate in patient intake which includes gathering patient information such as vitals, patient history, etc.. Safely escort patients to the laboratory for diagnostic testing or specimen collection.. Support clinical staff during specimen collection, including blood draws, urine samples, or other diagnostic procedures, while maintaining patient comfort and safety.
Clinical Research Intern. ICON plc is a world-leading healthcare intelligence and clinical research organization.. Performing clinical requirements of study protocols, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, pulmonary function testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or coordinator.. Assisting the Clinical Research Coordinator or other staff members with creating and copying patient files for study closeout procedures.. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
It is our mission as a family-based organization to revolutionize the healthcare industry through a culture of resident centered healthcare services, personalized spirituality, and real quality of life initiatives. Signature HealthCARE is a family-based healthcare company that offers integrated services in 7 states across the continuum of care: skilled nursing, rehabilitation, assisted living, memory care, home health, cognitive care, and telemedicine. Many of our skilled nursing facilities have achieved a 4 or 5-star overall rating from the Centers for Medicare & Medicaid Services. To learn more about our benefits offered, please contact Jenny Collins, Senior Director of Talent Acquisition, directly at (561).. Our culture is built on three distinct pillars: Learning, Spirituality and Intra-preneurship.
The role requires a commitment to patient safety, dignity, and comfort while maintaining a compassionate, respectful and professional attitude.. Knowledge of patient care practices and basic anatomy and physiology.. Ability to effectively use standard medical equipment (e.g., blood pressure cuff, thermometer, stethoscope).. Excellent communication and interpersonal abilities, proficiency in electronic health records (EHR) systems.. Adherence to Holy Cross Medical Center policies surrounding patient safety, infection control and HIPAA.
Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.. Referral services for child, elder and pet care, home and auto repair, event planning and more. Healthcare experience should be recent and within a clinical setting such as Hospital, Ambulatory Surgery Center, etc.. Other specialized programs include our Sleep Center at Fairview Park, the Same Day Surgery Center, the Heart Center at Fairview Park, the Women's Imaging Center and much more.. HCA Healthcare Co-Founder
The Patient Care Technician position on G18- Stem Cell Transplantation & Cellular Therapy unit at MD Anderson Cancer Center provides patient care services as assigned by a registered nurse, and directly impacts patient comfort and outcome of care. Ideal candidate must have a high school diploma and either one year of recent experience in an acute care setting as a Nursing Assistant or a CNA certification. The Inpatient Stem Cell Transplant & Cellular Therapy unit is a 48 bed unit and is one of our designated immunotherapy floors, administering research protocols involving immunotherapy and CARTOX therapy to patients, including Phase 1 clinical trials. Teachers Retirement System defined-benefit pension plan and two voluntary retirement plans.. Relocation Assistance Available?
Join to apply for the Associate Director, Medical Writer role at MannKind Corporation.. Partner with cross-functional teams, including clinical development, medical affairs, regulatory affairs, safety to ensure seamless integration of medical writing. Minimum of 5 years relevant industry experience in medical writing in sponsor/CRO setting or academia, or related areas such as quality, regulatory submissions, publications, clinical research, or product support/R&D. Experience working on publications for multiple therapeutic areas, endocrinology and pulmonology preferred. Sweetwater Veterinary Clinic - Medical DirectorAssociate Director to Director, Statistical Programming
To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group researches, develops and markets innovative drugs in its three therapeutic areas: AIR (products and services that promote respiration, from new-born to adult populations), RARE (treatment for patients with rare and ultra-rare diseases) and CARE (products and services that support special care and consumer-facing self-care).. Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent specialty and rare disease markets.. We are a B Corp and Benefit company awarded Top Employer status for six consecutive years and certified as a Great Place to Work. At Chiesi, we share an entrepreneurial spirit and act as a force for good, pursuing high social and environmental standards, to ensure the wellbeing of our people, patients, and communities.. Ensure appropriate implementation of Chiesi Global Rare Disease procedures for the regulatory aspects of labeling preparation, launch prep, review, approval, and submission.. Experience with Veeva Vault PromoMats and MedComms, Trackwise, or similar document management systems a plus
Responsibilities Clinical Program Leadership: Design, implement, and medically monitor clinical trials (Phase 1-3) for oncology assets.. Cross-functional Collaboration: Work closely with research, preclinical development, regulatory affairs, biostatistics, data management, clinical operations, and commercial teams to ensure seamless program execution.. Minimum of 10+ years of clinical drug development experience in the biotechnology or pharmaceutical industry, with a focus on oncology biologics.. Demonstrated success in leading and managing clinical trials from early to late-stage development.. Strong understanding of clinical trial design, biostatistics, medical monitoring, and regulatory requirements (FDA, EMA, ICH guidelines).
Reporting to the Chief Medical Officer, the Pharmacovigilance Scientist at Cellectis will manage all activities related to the performance of drug safety at Cellectis.. drug safety is pro-actively integrated into drug development activities. Manage interface with drug safety meetings (PV team, DSMB/DMC and SAC meetings). Educate the organization on critical developments and regulatory guidance related to drug safety (FDA, EMA, MHRA, PMDA and others, where necessary). Minimum of 7-10 years of relevant experience in pharmacovigilance, drug safety, regulatory affairs or clinical trials
The licensed Clinical Content Developer RN, NP, PA develops and updates the clinical content of Optum Clinical Products.. The Clinical Content Developer is also responsible for quality assurance (QA) of the content and for responding to internal and external client questions and concerns.. We are looking for a licensed RN, NP, or PA, with a broad clinical background who can join our fully remote team and collaborate with us on the development of quality content for the InterQual suite of products.. Collaborate with Product Development (PD), Product Management (PM), Product Owner (PO), and Business Systems Analyst (BSA) as needed. Experience with utilization management (UM), case management, or use of evidence-based guidelines such as InterQual/Clinical Decision Support applications or Medicaid State Policies.
· Juris Doctor (JD) from an accredited U.S. law school; active license to practice law in at least one U.S. jurisdiction.. · Strong knowledge of drug development, clinical trials, and FDA regulatory processes.. · Familiarity with accelerated approval pathways, surrogate endpoints, and data privacy regulations (e.g., HIPAA, GDPR).. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process.. Similar Jobs (2) Senior Director, Nonclinical Toxicology and ADME locations PA - Conshohocken - Office time type Full time posted on Posted 2 Days Ago Director, Content and Training, Medical Affairs locations PA - Conshohocken - Office time type Full time posted on Posted 17 Days Ago
The incumbent might also be designated as U.S. Agent (back-up) for the U.S. Office for both ANDAs (GPI USA) and API (GLS India).. Support the U.S. Office for more than 170 approved ANDAs and all unapproved (under review ANDAs) as U.S. Agent back-up for all Glenmark subsidiaries including GPL, GSSA, GPI and GLS. The successful candidate will need to be able to review and sign various submissions to FDA. It will include ANDA cover letter, Form 356H for Original ANDAs, Amendments to ANDAs and/or Supplements to post-approval work.. The email list is provided for such communications which includes Commercial Division Heads, R&D, QA, Legal, Business Development, Project Management, Demand Planning, Marketing and others identified on the list.. Separate communications received from the FDA to support GLS will be sent to the GLS leadership team as identified.. B.S. in Chemistry or Biology, or Engineering degree in Biotechnology or Chemical Engineering
This will include the planning and execution of quantitative analyses which may include population pharmacokinetics and pharmacokinetics (PK)/pharmacodynamics (PD) exposure response.. PhD in Pharmaceutical Science, Math or related discipline preferred.. Demonstrated ability to work across functions including medical writing, clinical operations, biometrics, clinical development, quality and regulatory affairs.. Neurodivergence, for example, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, dyslexia, dyspraxia, other learning disabilities. Traumatic brain injury
About Synchron Synchron is a neurotechnology company with a mission to deliver the first commercially scalable brain-computer interface (BCI) for millions of people with paralysis to reconnect with the world.. Our minimally invasive BCI system is designed to enable users to control digital devices directly through thought, restoring access and control over the digital world.. Develop and execute calibration procedures for production and test equipment to ensure measurement accuracy and compliance with quality standards; maintain detailed records of calibration activities.. In addition to base pay, this role may be eligible for discretionary bonuses and/or equity grants subject to board approval and company policy.. Discretionary unlimited PTO
We are seeking a detail-oriented, strategic, and experienced Accounts Receivable Director to lead and manage the revenue cycle process in our skilled nursing facility home office.. This leadership role ensures timely and accurate billing, collections, and cash posting for all payer types including Medicare, Medicaid, Managed Care, and Private Pay. The AR Director plays a critical role in maintaining financial health, regulatory compliance, and operational efficiency.. Oversee all aspects of accounts receivable, including billing, collections, payment posting, and reconciliation.. Monitor aging reports, reduce Days Sales Outstanding (DSO), and implement effective collection strategies.. Proficiency in EHR systems and AR software (e.g., PointClickCare, MatrixCare, or similar platforms).