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Organizing data
You will supervise nursing care provided by registered nurses, licensed vocational/practical nurses and STNA/CNAs.. - Director of Nursing, management or supervisor experience in long-term care, restorative or geriatric nursing.. About Ciena Healthcare. Ciena Healthcare is Michigan’s largest provider of skilled nursing and rehabilitation care services.. If you have a passion for improving the lives of those around you and working with others who feel the same way, Ciena is the place for you!
Whether your abilities are in direct patient care or one of the many other areas of healthcare administration and support, everyone at Parkland works together to fulfill our mission: the health and well-being of individuals and communities entrusted to our care.. - Must be able to demonstrate a working knowledge of laws and regulations governing Medicare, Medicaid and other funding sources.. Manages clinical denials, educating referring providers on clinic and payor requirements.. Oncology Services Only: Will maintain current Commission on Cancer specific certification in the nurse's specialty by an accredited certification program or will continue ongoing education by earning 12 cancer-related continuing education nursing contract hours per year or 36 cancer-related continuing education nursing contract hours each accreditation cycle (3 years).. As part of our commitment to our patients and employees' wellness, Parkland Health is a tobacco and smoke-free campus.
Whether your abilities are in direct patient care or one of the many other areas of healthcare administration and support, everyone at Parkland works together to fulfill our mission: the health and well-being of individuals and communities entrusted to our care.. - Must be able to demonstrate a working knowledge of laws and regulations governing Medicare, Medicaid and other funding sources.. Manages clinical denials, educating referring providers on clinic and payor requirements.. Oncology Services Only: Will maintain current Commission on Cancer specific certification in the nurse’s specialty by an accredited certification program or will continue ongoing education by earning 12 cancer-related continuing education nursing contract hours per year or 36 cancer-related continuing education nursing contract hours each accreditation cycle (3 years).. As part of our commitment to our patients and employees’ wellness, Parkland Health is a tobacco and smoke-free campus.
Ensure coding accuracy and compliance with CMS, Medicare, Medicaid, and state-specific requirements. Requirements:CPC (Certified Professional Coder), CCS (Certified Coding Specialist), CCA (Certified Coding Associate), or CRC (Certified Risk Adjustment Coder). Associate's or Bachelor's degree in Health Information Management, Medical Coding, or a related field preferred. 3+ years of ICD-10 coding experience in long-term care (LTC), skilled nursing (SNFs), assisted living, or senior living settings. Familiarity with Electronic Health Record (EHR) systems and coding software.
Clinical Research Supervisor/Protocol Project Manager – Radiation Oncology Join to apply for the Clinical Research Supervisor/Protocol Project Manager – Radiation Oncology role at University of California, San Francisco.. The UCSF HDFCCC is a fast-paced environment, and the successful candidate will be an independent, detail-oriented individual with drive and focus.. The UCSF Helen Diller Family Comprehensive Cancer Center is one of two NCI-designated comprehensive cancer centers in the Bay Area, focusing on laboratory research, clinical translation, patient care, and population health, guided by precision medicine principles.. Knowledge of clinical research protocols, IRB, FDA regulations, and oncology terminology. Experience with oncology trials, UCSF research environment, and systems like OnCore and EPIC
Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera’s mission to advance novel therapies for obesity and related conditions.. Playing a critical hands-on role within Kailera, the Associate Director, Clinical Quality Assurance will be relied upon as Subject Matter Expert in GCP and GVP Compliance with respect to the planning, document review, execution, and close-out of Clinical Studies and related drug safety.. Plan, coordinate, review and approve internal, external, and clinical site audits using risk-informed strategy to ensure GCP/GVP compliance in clinical studies and pharmacovigilance operations.. Serve as a subject matter expert on GCP/GVP quality assurance matters.. Previous hands-on experience with Veeva Quality Docs, Veeva Training, and Veeva QMS required.
From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments.. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery.. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence.. Track timelines and documents milestone achievements for inclusion in regulatory submissions.. May interact with regulatory agencies as part of submission review and on-site audit support.
This position is responsible for assisting the Director of Quality, Patient Safety and Regulatory affairs with the coordination and oversight of regulations and standards governing the hospitals set forth by all Regulatory Agencies, evaluation activities and the survey process.. Serve as a contact with The Joint Commission and DPH. Professional in Healthcare Quality (CPHQ). Saint Francis Hospital is committed to exceeding the expectations of our patients and families by providing world-class service in a progressive, people-centered, compassionate health care environment.. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care.
As a RN Clinical Research Specialist in Outpatient Infusion, you will play a vital role in delivering direct patient care and administering investigational therapies in both early phase clinical trials, following established research protocols.. With comprehensive electronic medical records, physician order entry, digital radiography and proprietary advanced patient monitoring, Banner Gateway provides you with the innovative resources you need to provide your patients with the best care possible.. Located near Phoenix in Gilbert, Ariz., Banner Gateway Medical Center offers 286 private rooms, 13 operating suites, a 46-bed emergency department and shares a campus with the Banner MD Anderson Cancer Center.. Banner MD Anderson Cancer Center Located in Gilbert, Ariz. (the Phoenix Metro area) on the Banner Gateway Campus, the center provides world-class care for oncology patients - both inpatient and outpatient - and has also brought leading oncology programs to the Banner Gateway campus including designation as a Stem Cell Transplant Center of Excellence and comprehensive Head & Neck cancer care.. Our capabilities include five linear accelerator vaults, a brachytherapy vault, an advanced diagnostic imaging suite with PET/CT scan, more than 70 infusion bays, a cryopreservation lab and much more.
The Patient Safety Associate (PSA) provides 1:1 safety observation and basic direct patient care, under the direction of the RN to include, but not limited to direct visual observation, verbal re-direction, safety checks, environment check care and comfort, personal care and hygiene, ADLs and mobility/fall prevention.. Provides 1:1 safety observation for patients requiring safety observation, including, but not limited to high risk suicidal, psychiatric, medical and surgical compromised patients with dementia, delirium, traumatic brain injury, substance abuse withdrawal and other diagnoses for potential patient harm.. Under the direction of RN or independent licensed practitioner, the Patient Safety Associate provides safe and direct care to patients on their assigned units making age appropriate adjustments as needed.. Upon discovery, the Patient Safety Associate immediately reports any incident posing harm or threat to a patient to the supervising RN or independent licensed practitioner.. Current enrollment (or planned) in accredited school in healthcare and/or humanities related associates or baccalaureate IE: Nursing, Medical, PT/OT, Pharmacy, Health Administration, Dental, Nutrition, PA, Psychology, Sociology, Biology, Chemistry, Forensics
The ideal candidate will have a strong background in healthcare administration, regulatory compliance (Medicare Conditions of Participation), clinical coordination, and business operations.. Manage all aspects of the agencys clinical and administrative operations, including staff supervision, patient care coordination, budgeting, and resource allocation.. Ensure appropriate supervision and support of clinical staff including RNs, PTs, OTs, SLPs, MSWs, HHAs, and administrative personnel.. Bachelor's degree in a healthcare-related field or current clinical licensure (e.g., RN, PT, OT) required; Masters degree preferred.. Comprehensive knowledge of Medicare regulations, OASIS documentation, HIPAA, and CMS guidelines.
Otsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better health worldwide.". Otsuka researches, develops, manufactures and markets innovative products, with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for the maintenance of everyday health.. Otsuka maintains a hybrid work policy and travel is expected 20% of the time based on business needs.. Work with bioanalytical team members on activities related to sample management, pharmacogenomics and biomarker development and provide analysis support related to PK, PBPK and PK/PD.. Work with formulation development groups and provide support for PK and PK/PD activities related to formulation development, in vivo-in vitro correlations and biowaivers for pre- and post-approval formulations.
The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.. Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords). A minimum of 3 years prior Clinical Research Coordinator experience required. Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator. Care Access does not engage in any unfair or forced labor practice and does not tolerate, under any circumstances, the use of any form of forced or involuntary labor, child labor, or human trafficking.
We are seeking a dedicated and experienced MDS Manager to lead our clinical documentation and reimbursement efforts in our long-term care facility.. Maintain current MDS status for all residents in compliance with state/federal regulations (OBRA, Medicare PPS, Medicaid payment systems).. Provide ongoing MDS/RUGs training and education to staff.. RNAC certification preferred.. Strong working knowledge of MDS, PPS, Medicare/Medicaid regulations, and long-term care standards.
Communicate with relevant global team members, other B&L departments (e.g., R&D/Project Management, Clinical/Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/Device Safety, and Clinical Supplies), and external consultants to ensure study objectives are being met and provide the operations director and/or senior management with timely updates on progress and changes in scope, schedule, and resources.. Responsible for the quality of all study-related documentation (e.g., Trial Master File, site qualification and initiation visits reports, interim monitoring visit reports, clinical monitoring plan, informed consents, CRF completion guidelines, pharmacy manual, etc.). during study start-up and throughout the life of the project to ensure that procedures are followed in an appropriate and consistent manner.. Liaise with PVG/GPSS and provide clinical operations support and guidance for the ongoing surveillance of the safety of patients in clinical trials by reviewing reported AEs and SAEs and assure proper reporting of the events to the IRBs/REBs/ECs.. Strong knowledge of Good Clinical Practices (GCP), clinical trials management (including site monitoring), scientific methods, research design, regulatory compliance, and clinical data management.
Strategic Planning: Develop and execute a comprehensive QA strategy that encompasses manual and automated testing across all product lines (deposits, lending, fraud & risk management, etc.). , channel types (web, mobile, API, batch data feeds, AI & models, etc.). Get notified about new Director of Quality Assurance jobs in Morristown, NJ.. Director of Quality Assurance - Aseptic CDMO Director, Clinical Quality Assurance (GCP) Nutley, NJ $200,000.00-$250,000.00 1 week ago. Associate Director, Volunteer Communications & Marketing Clinical Director - Outpatient Mental Health Facility Clinical Director - Outpatient Mental Health Facility Director of Patient Services/ Registered Nurse Madison, NJ $115,000.00-$171,080.00 1 week ago
Passionate about precision medicine and advancing the healthcare industry?. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.. The Director, CRO Quality Assurance (QA) is responsible for the management and oversight of Tempus Compass', our Clinical CRO subsidiary, Quality Management System (QMS) and QA program.. Conduct audits, including Internal, Investigator Site and Trial Master File.. Director, Clinical Quality Assurance (Gene Therapy) California, United States $221,300.00-$420,500.00 1 week ago
Our Project Delivery colleagues within our PPD clinical research services direct, coordinate and manage the technical and operational aspects of projects, securing the successful completion of clinical trials.. Therapeutic scopes include: infectious and respiratory diseases, oncology/hematology, neurosciences, cardiovascular and metabolic, general medicine and vaccines.. Accountable for strategic indication or client-specific portfolio management within a Therapeutic Unit.. Advanced, broad understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management; expert knowledge of ICH and other global regulatory guidelines; in-depth understanding of a regulatory specialty areas, such as preclinical, clinical, CMC, publishing, etc.. Expert financial acumen with an in-depth knowledge and practical application of budgeting, forecasting and resource management
Associate Director, Regulatory Affairs Advertising & Promotion (Hybrid or Remote) Associate Director, Regulatory Affairs Advertising & Promotion (Hybrid or Remote) role at AbbVie. This position leads cross-functional, multidisciplinary teams and drives regulatory advertising and promotion strategy for the US market.. Qualifications Bachelor’s Degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology, nursing). Relevant Master’s or Ph. D. or advanced scientific or law degree preferred. We strive to have a remarkable impact on people\'s lives across key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in the Allergan Aesthetics portfolio.. Industries Pharmaceutical Manufacturing and Biotechnology Research
As our Associate Director, Global Regulatory Affairs Advertising and Promotion lead you will act as the Subject Matter Expert for assigned products and projects focusing on advertising and promotion regulatory affairs.. You will be the Regulatory Advisor and function as the "R" in the core Medical, Legal, and Regulatory review functions within the Commercial Material Review Process (CMRP).. You will be product or project business lead for global CMRP at Takeda. CMRP Meeting Chair - pausing to communicate comments to coordinator, diffusing team disputes, serving as a dependable negotiator, keeping team focus on our ultimate stakeholders which are the patients who trust us to do the right thing, and overseeing escalation steps if MLR cannot come to alignment or if there is new data or campaigns that require senior level management input or alignment.. Exercise decision-making authority within the CMRP to ensure compliance, patient safety, and alignment with Takeda's values.