Collecting information
Organizing data
The Clinical Research Nurse will work under the supervision of Clinical Research Management and the Principal Investigators (PI). The Clinical Research Nurse will also assist in planning, monitoring, and assessment of clinical development and operational research projects as assigned. Performs nursing assessments and monitor subjects' progress during clinical trials and notify principal investigator of any adverse events and serious adverse events, including evidence of drug toxicity or unexpected side effects. Performs and/or oversee a variety of clinical duties that may include administration of research study drugs, EKGs, vital signs, physical exams/assessments, processing/shipment of biological specimens, chemistries and recording the results in the subject study chart. This may include communicating with private and pharmaceutical company personnel and the clinical research unit.
Jump-start your career as a(an) Division Director of Pharmacy Operations today with HealthTrust Supply Chain.. 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.. Free counseling services and resources for emotional, physical and financial wellbeing 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service) Employee Stock Purchase Plan with 10% off HCA Healthcare stock Family support through fertility and family building benefits with Progyny and adoption assistance.. Assist in the development, implementation and sustainment of charge master standardization to maximize revenue capture and reduce billing errors.. - Dr. Thomas Frist, Sr. HCA Healthcare Co-Founder If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Division Director of Pharmacy Operations opening.
The Administrative Nursing Supervisor facilitates timely and safe patient flow and provides management and operational oversight of the acute care hospital setting, and ensures the provision of safe, quality patient care.. We are a locally owned, not-for-profit healthcare system comprised of nin hospitals, a statewide health plan and a growing multi-specialty medical group.. Our health plan serves more than 640,000 members statewide and offers Medicare Advantage, Medicaid (Centennial Care) and Commercial Health Plans.. Nestled between tall pines and mountain vistas at an elevation of 6,900 feet, Ruidoso is a mountain oasis in southern New Mexico.. AA/EOE/VET/DISABLED. PHS is a drug-free and tobacco-free employer with smoke free campuses.
While candidates from anywhere in California are welcome to apply, there is a strong preference for those who reside on the Central Coast (Ventura, Santa Barbara, San Luis Obispo, Monterey, and Santa Cruz Counties).. Contribute in the new implementation and review of documented audit processes to ensure compliance against requirements including contractual, Federal, State, the Centers for Medicare and Medicaid Services (CMS), and the National Committee for Quality Assurance (NCQA) standards.. Develops audit scope and audit tools based on regulatory compliance against state and federal regulatory requirements and standards, including those issued by the California Department of Health Care Services (DHCS), the California Department of Managed Health Care (DMHC), NCQA, and CMS requirements.. Audits to ensure compliance with Federal and State regulatory requirements, the DHCS Medi-Cal Managed Care Contract, Medicare Advantage and Medicare Part D regulations and guidance, the DHCS State Medicaid Agency Contract (SMAC), Delegation Agreement, Health Plan Management System (HPMS memos, All Plan Letters (APLs), Policy Letters (PLs), CenCal Health policies and procedures, and National Committee for Quality Assurance (NCQA) standards, as applicable.. Extensive audit experience with DHCS, CMS, DMHC, and/or NCQA and understanding of audit standards and requirements;
As the preeminent institution in western Pennsylvania for the delivery of cancer care, the performance of basic, translational, and clinical research, and the education of the next generation of cancer researchers and physicians, UPMC Hillman Cancer Center is exceptionally well-positioned to contribute to the global effort to reduce the burden of cancer. UPMC Hillman Cancer Center is currently hiring a regular full-time Clinical Research Nurse Coordinator (RN) to help support the Community Oncology Clinical Research Services (CRS) teams at our UPMC Hamot Oncology network office located in Erie, PA. This position offers a $6,000 sign-on bonus and will work a regular Monday through Friday daylight schedule with the Hamot Oncology network location. This unique role allows for the clinical research nursing professional to work in the community and screen/enroll patients in all cancer disease centers with UPMC Hillman Cancer Center working as a Trials Coordinator. The clinical research coordinator will work with physicians, nurses, other allied health professionals, and research staff to coordinate clinical research efforts provided at UPMC. Using a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing.
As the preeminent institution in western Pennsylvania for the delivery of cancer care, the performance of basic, translational, and clinical research, and the education of the next generation of cancer researchers and physicians, UPMC Hillman Cancer Center is exceptionally well-positioned to contribute to the global effort to reduce the burden of cancer.. UPMC Hillman Cancer Center is currently hiring a regular full-time Clinical Research Nurse Coordinator (RN) to help support the Community Oncology Clinical Research Services (CRS) teams at our UPMC Hamot Oncology network office located in Erie, PA. This position offers a $6,000 sign-on bonus and will work a regular Monday through Friday daylight schedule with the Hamot Oncology network location.. This unique role allows for the clinical research nursing professional to work in the community and screen/enroll patients in all cancer disease centers with UPMC Hillman Cancer Center working as a Trials Coordinator.. The clinical research coordinator will work with physicians, nurses, other allied health professionals, and research staff to coordinate clinical research efforts provided at UPMC. Using a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing.
Required Qualifications:Bachelors degree in Nursing, Social Work, Healthcare Administration, or a related field. Familiarity with electronic health records (EHR) systems and case management software. Preferred Qualifications:Certification in Case Management (CCM, ACM, or equivalent). Familiarity with chronic disease management and transitional care planning. Benefits & Perks:Fully remote work environment with flexible hours.
Quality Assurance Analyst. Should be able to communicate and publish status reports of all open issues and gaps found during test phase and articulate the details to the Development teams.. Deep knowledge of healthcare operations (preferably Medicaid), business processes. Proficient in Atlassian tool suite including JIRA and Confluence. Prior experience working in a standard SDLC (waterfall methodology) & in an AGILE delivery.
As we expand our in vivo research capabilities, including a variety of preclinical studies, we are seeking an experienced Director, GLP Quality Assurance & Compliance to establish and lead a Quality Assurance Unit (QAU).. Additionally, they will play a key role in supporting in vivo research protocols and procedures procedures, ensuring that all processes align with in vivo and in vitro GLP studies and animal welfare regulations.. Establish robust SOPs, policies, and procedures to align the entire facility with GLP principles and regulatory best practices of an in vivo and in vitro preclinical testing facility.. Quality Oversight of In Vivo and In Vitro Research OperationsProvide regulatory and quality oversight of in vivo preclinical studies, ensuring adherence to GLP regulations and animal welfare standards (USDA, OLAW, AALAC, IACUC).. Experience developing and implementing quality programs as well as daily execution for in vivo preclinical research, surgical procedures, and regulatory compliance.
The Clinical Research Nurse will work under the supervision of Clinical Research Management and the Principal Investigators (PI).. The Clinical Research Nurse will also assist in planning, monitoring, and assessment of clinical development and operational research projects as assigned.. Performs nursing assessments and monitor subjects' progress during clinical trials and notify principal investigator of any adverse events and serious adverse events, including evidence of drug toxicity or unexpected side effects.. Performs and/or oversee a variety of clinical duties that may include administration of research study drugs, EKGs, vital signs, physical exams/assessments, processing/shipment of biological specimens, chemistries and recording the results in the subject study chart.. This may include communicating with private and pharmaceutical company personnel and the clinical research unit.
Strong Patient Safety Ratings - Consistently ranked highly by Leapfrog for patient safety and named a high-performing hospital for COPD care by U.S. News & World Report.. Community Impact - We invest over $14 million annually into Charles County, supporting health access, food insecurity programs, stroke prevention education, senior wellness, and chronic disease management.. Apply Today and be part of a high-quality, patient-focused hospital with a commitment to excellence and community impact.. Maryland Nursing Assistant Certification required as well as completion of one of the following training programs: hospital-based program, community college, Emergency Medical Technician, Medical Corpsmen.. Employees with work experience that provide on the job training equivalent to the above programs can be considered as a substitute to a formal PCT training program.
1 to 2 years of previous insurance verification, pre-certification/pre-authorization, medical billing, or other related experience in healthcare environment.. Patients and their families receive expert, compassionate care through the system’s 305-bed Stamford Hospital; Stamford Health Medical Group, with more than 40 offices in lower Fairfield County offering primary and specialty care; a growing number of ambulatory locations across the region; and support through the Stamford Hospital Foundation.. The Centers for Medicare and Medicaid Services (CMS) rated Stamford Hospital as a five-star hospital for Overall Quality and The Leapfrog Group awarded Stamford Hospital an “A” for patient safety.. Additionally, in 2020 Stamford Health’s Carl & Dorothy Bennett Cancer Center entered into an expanded collaboration with Dana-Farber Brigham Cancer Center.. Our collaborative with Hospital for Special Surgery, and the Dana Farber Brigham and Women's Cancer Care Collaborative, connect us directly with world class expertise, research, resources and technology to put us at the forefront of patient care.
As Scientist 3, you will be responsible for the translation and implementation of (non-medical) scientific concepts into the study design and/or program across planning, execution, and reporting, including integration of biomarkers, digital technologies, data science initiatives, and select vendors.. PhD in relevant field (e.g. Neuroscience, Biomedical Sciences, Biology; chemistry: pharmacy) OR. Responsible for identifying and implementing (non-medical) scientific aspects of the program and/or study at planning, execution and reporting, including (but not limited to) integration of Biomarkers and Data Science/Digital Health initiatives into studies.. Along with SRP or Clinical Leader and global development partners, responsible for oversight and high-quality implementation and closure of the study, ensuring data integrity.. In concert with operational staff, acts as a liaison between the company and clinical investigators for overarching scientific guidance and other potential non-medical aspects.
Our award-winning products are sold in thousands of retail and eCommerce stores nationwide, including Walmart, Amazon, Walgreens, Target, CVS, The Vitamin Shoppe, Sam’s Club and iHerb. Force Factor is based in Boston’s innovative Seaport District. Force Factor is seeking a sharp, detail-driven Quality & Regulatory Compliance Manager to lead and oversee all regulatory and quality assurance efforts for our growing portfolio of dietary supplements and vitamins. 5+ years of experience in regulatory affairs or quality assurance within dietary supplements, CPG, or pharmaceuticals.. Strong knowledge of U.S. regulations governing dietary supplements (FDA, DSHEA, cGMPs, etc.)
If you’ve led QMS programs, represented a site during audits, and thrive on being the go-to authority for compliance and quality excellence—this is your chance to make a big impact.. Oversee the preparation, documentation and conduction of Quality Assurance audits of Distribution Centers, joint Ventures, X-Ray Centers, private label manufacturers, non-manufacturing suppliers of Medical Devices and Pharmaceuticals. Serve as FDA Official Correspondent for US Facilities and US Agent for foreign HS entities.. Assist with due diligence and follow-up surveillance audits as required and serve as SME for some manufacturing partners.. RAPS and ASQ or other equivalent Certifications preferred.
Manage and oversee clinical and administrative workflows including documentation of referrals, DME pickups, Medicare eligibility, insurance verifications, and patient benefit tracking.. We are a national leader in home-based care with more than 430 locations across 36 states.. Wellness Programs (Telemedicine, Diabetes Management, Joint & Spine Concierge Care).. Education Support & Tuition Assistance (ASN to BSN, BSN to MSN).. Keywords: hospice RN manager, patient care manager senior, hospice leadership jobs, RN leadership, home-based care oversight, hospice case management, Gentiva careers
At TEKsystems, we are working with a local company seeking a Claims Manager who will oversee claims processing operations, ensuring accuracy, efficiency, and regulatory compliance.. The Claims Manager will manage both onshore and offshore vendor relationships to ensure seamless operations across all lines of business, including Medicare, Medicaid, and commercial insurance.. Claims Processing: Oversee end-to-end claims processing operations, with experience in Claims systems (QNXT).. System Implementation: Integrate Cotiviti, track testing, and incorporate into workflows.. Team Management: Lead and mentor ICT testers and liaisons.
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
Executive Director/Vice President, Regulatory Affairs Join to apply for the Executive Director/Vice President, Regulatory Affairs role at Keros Therapeutics. With a focus on developing differentiated product candidates that are designed to alter TGF-β signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue.. Reporting to the CMO, the ideal candidate will be responsible for developing and delivering innovative, breakthrough global regulatory strategies for product development and approval, in alignment with the global business strategy.. Direct Keros’s global clinical, non-clinical, and CMC regulatory strategies. Supervise, interact with and/or coordinate with regulatory team and external service providers to ensure adequacy of project support and deliverables
Wellness Programs (Telemedicine, Diabetes Management, Joint & Spine Concierge Care). Education Support & Tuition Assistance (ASN to BSN, BSN to MSN). Keywords: hospice RN manager, patient care manager senior, hospice leadership jobs, RN leadership, home-based care oversight, hospice case management, Gentiva careers. At Heartland Hospice, part of Gentiva, it is our privilege to offer compassionate care in the comfort of wherever our patients call home.. Our nationwide reach is powered by a family of trusted brands that include: Hospice care: Gentiva Hospice, Emerald Coast Hospice Care, Heartland Hospice, Hospice Plus, New Century Hospice, Regency SouthernCare, SouthernCare Hospice Services, SouthernCare New Beacon