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Medical Oncologist - GI Malignancy Program Leader Location: Charlotte, NC We are seeking a board-certified or board-eligible Medical Oncologist to lead our GI Malignancy program in Charlotte, NC. This is an exciting leadership opportunity in a growing cancer program committed to excellence in patient care, research, and innovation.. Work in a state-of-the-art, multi-million-dollar Cancer Institute facility in uptown Charlotte.. Collaborate with colorectal surgery, hepatobiliary surgery, radiation oncology, and other GI-specific subspecialists.. Strong interest in clinical research, with experience in early-phase clinical trials preferred.. Enjoy world-class dining, cultural attractions, professional sports, and green spaces like Freedom Park and the Carolina Thread Trail.
This care may be in clinic or virtually, via telemedicine.. May serve as direct caregiver, health care consultant, patient educator, administrator, or researcher.. Completes patient charge capture and medical record documentation in a timely fashion.. Often serves as a resource for nursing staff by providing information being studied in clinical trials.. Provides palliative care for the patient and their families as needed.
Additionally, the Patient Care Technician may assume the responsibilities of a health unit coordinator.. Every other weekend and two summer/ two winter holiday rotation.. Department/Unit: Inpatient Hospice.. May assume the responsibilities of a health unit coordinator, including answering phones, transcribing physician orders, managing unit records, organizing, stocking, and maintaining unit supplies.. For those hired into a skilled nursing facility or long-term care center, obtaining a certification within 120 days allowed only if the new hire has never been a in Utah. If previously certified, hire must have a current and valid certification before the start date.
Kernodle Clinic's Walk-In Clinic in Burlington, NC, is seeking a Family Practice or Internal Medicine physician to join their team of four physicians and two mid-level providers.. Patient Demographics: Payor mix includes 33% BCBS, 28% Managed Care, 21% Medicare, 6% Workers Comp, and 5% Medicaid.. Onsite Resources: Access to onsite lab and x-ray facilities for convenient patient care.. Legacy of Excellence: Affiliated with Duke University Health System since 2013 and serving Burlington for 75 years, Kernodle Clinic is a trusted healthcare provider.. Elon University is consistently ranked as one of the most beautiful campuses in the country by Best College Review and was named the Best Run College by The Princeton Review.
Masters in Business Administration, Public Health, Healthcare Administration, etc.. Peer Review, medical policy/procedure development, provider contracting experience.. Experience with NCQA, HEDIS, Medicaid, Medicare and Pharmacy benefit management, Group/IPA practice, capitation, HMO regulations, managed healthcare systems, quality improvement, medical utilization management, risk management, risk adjustment, disease management, and evidence-based guidelines.. Molina Healthcare offers a competitive benefits and compensation package.. Molina Healthcare is an Equal Opportunity Employer (EOE) M/F/D/V.
The Medical Director will be responsible for utilization review case management for Medicare and Medicaid in the California market while also assisting in the Washington Medicaid market. Unless expressly allowed by state or federal law, or regulation, must be located in a state or territory of the United States when conducting utilization review or an appeals consideration and cannot be located on a US military base, vessel or any embassy located in or outside of the US. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act. Behavioral Health Medical Director- Child Psychiatrist.. Previously known as Anthem, Inc., we have evolved into a company focused on whole health and updated our name to better reflect the direction the company is heading.
Regulatory & Market Access : Lead or collaborate on the regulatory approval process, ensuring compliance with FDA, CE Mark, and other global regulatory bodies for AI-based medical devices.. Global Collaboration : Engage with top-tier pharma and healthcare institutions worldwide.. Flexible Work Options : Enjoy flexible working hours and remote work opportunities.. 3+ years of experience in clinical practice, medical devices, digital health, or AI-driven healthcare technologies.. Experience in clinical research and validation, particularly with AI-based healthcare solutions, medical imaging, or digital therapeutics.
Home Infusion Specialty Pharmacy. We are seeking an experienced and detail-oriented Medical Biller with specialized knowledge in home infusion pharmacy billing.. Bill and reconcile nursing per diem charges and infusion drug charges under Medicare Part D and commercial payers.. Minimum of 2 years of recent experience in medical billing for a home infusion pharmacy setting.. Familiarity with Medicare Part D and commercial insurance billing practices.
Wage: $22-$27 DOEDescriptionWe are seeking a diligent and detail-oriented Medical Records professional to join our team at Colonial Vista Post Acute.. As a Medical Records professional, you will utilize cutting-edge technology to facilitate the effective management of electronic health records (EHR) and assist in the coordination of patient care by providing timely access to essential medical history.. Input and update patient information into electronic health record (EHR) systems promptly and accurately.. Working knowledge of ICD-10 codingStrong understanding of medical terminology and healthcare practices.. Proficiency in electronic health record (EHR) systems and other relevant software applications.
Provides leadership and clinical guidance to pharmacy technicians and other support staff.. Extensive pharmacology knowledge. Responsibilities Oversees and directs pharmacy technicians' and technician trainees’ workflow and verifies order entries.. Completes initial patient consults advising patients of their medication and responds to all patient inquiries.. Recognizes health issues that may interact with the patient's medication therapy.
Looking for a chance to drive measurable and meaningful improvement in the use of evidence-based medicine, patient safety, practice variation and affordability?. You can make a difference at UnitedHealth Group and our family of businesses in serving our Medicare, Medicaid and commercial members and plan sponsors.. UnitedHealth Group complies with all minimum wage laws as applicable.. In addition to your salary, UnitedHealth Group offers benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements).. We believe everyone–of every race, gender, sexuality, age, location and income–deserves the opportunity to live their healthiest life.
At Kelsey-Seybold Clinic, our Neurologists diagnose, treat, and manage patients with neurological disorders.. Kelsey Seybold Clinic has a 24-hour call center and after-hours registered triage nurse to assist in patient care.. About Kelsey-Seybold Clinic. Kelsey-Seybold Clinic is Houston’s premier multispecialty group practice, founded in 1949 by Dr. Mavis Kelsey in Houston’s renowned Texas Medical Center.. Kelsey-Seybold Clinic strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by organizational policy or by federal, state, or local laws unless such distinction is required by law.
Interim HealthCare is America’s leading provider of home care and healthcare staffing.. PRN / PART-TIME with opportunities to grow hours; DAYS / EVES / NOC. Registered Nurse (RN) Pay Rate: $45-$50 per hour, paid weekly. 24/7 on call representative from Interim Healthcare. Administer medication, operate medical equipment and maintain a safe environment
Area: Medical-CFP OT Class: PHTEC Shift: 1 Start: 07:30:00 End: 16:00:00. Accurately prepares unit dose medications, compounds a variety of pharmaceuticals under the supervision of a Pharmacist, including intravenous admixtures according to proper aseptic technique and in accordance with, professional standards and departmental policies and procedures, in order to maintain required levels of supply and to provide patients with needed medications;. Records billing information for accurate and appropriate billing of patients for medications, involving use of desktop computer keyboard for entering medication orders and billing information;. Inspects and stores delivered stock in the pharmacy patient care areas by sorting and shelving them for optimal retrieval;. Uses, maintains, and troubleshoots automated dispensing equipment or relevant pharmacy-related software and other equipment necessary for pharmacy operations;
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe.. From start to finish, we are involved in clinical studies – from crafting the study database to ensuring the pristine delivery of the final dataset.. With a variety of roles, from data support staff, to database and SAS programmers, coders, and functional leads, there are many opportunities to launch and further your career.. RN Clinical Nurse II - Nurse Connect - Remote RN Clinical Nurse Home Health - Hospice Services REMOTE - Quality Assurance Specialist (Clinical Research) Clinical Documentation Integrity Specialist *remote. Quality Assurance Specialist (Clinical Research) Senior Clinical Research Associate - Cystic Fibrosis/Nephropathy - East Coast - Remote Senior Clinical Research Associate - CNS/Ophthalmology - Upper Midwest - Remote Proposal and Contract Manager, USA, 12-18 months contract Oncology Sales Specialist, Raleigh, NC - Johnson & Johnson Innovative Medicine Sales, Territory Manager - Coronary Image Guided Therapy Devices (Raleigh, NC) We’re unlocking community knowledge in a new way.
Position Summary: The primary responsibilities of an Associate Director Medical Writer at include, but are not limited to, leading key medical writing projects and activities across therapeutic areas and preparing (under minimal supervision) scientific and regulatory documents related to the clinical development of investigational and marketed drugs and biologics.. These types of scientific and regulatory documents can include clinical study reports (CSRs), subject narratives, clinical investigator brochures, protocols, briefing documents, and sections of Investigational New Drug Applications (INDs) and New Drug Applications (NDAs)/Biologics License Applications (BLAs) (i.e., integrated summaries of safety and efficacy, product labeling, and summaries and overviews of nonclinical and clinical information).. Acts as medical writing point person for production of preclinical summaries, clinical summaries, pharmacokinetic reports, safety summaries, literature reviews, and other documents needed for regulatory submissions.. Liaises with internal groups, i.e., Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, Clinical Development, Clinical Operations and R&D Management to obtain necessary information and to ensure the timely implementation of activities related to the production of reports.. Knowledge of Common Technical Document content templates as well as content expectations for IND/NDA/MAA and other regulatory documentation.
Organize and support a cohesive and effective scientific communication and community-building strategy executed through multi-modal clinical education channels, including investigator meetings, publications, presentations, congresses, advisory boards, CME, speaker bureaus, and other channels. Gather feedback, data, or information during routine activities that can help the Company better comprehend medical or scientific needs, priorities, or concerns of healthcare practitioners (HCPs) and/or patients.. For Company-Sponsored Trials, collaborate and assist Clinical and Regulatory Affairs in reviewing study sites, identify potential investigators to participate in clinical development programs, identify barriers to patient enrollment and retention efforts to achieve study milestones, address questions from investigators and provide information regarding participation in company-sponsored clinical studies. 2+ years of experience within Medical Device and/or Biopharma Industry is a plus.. Experience in investigator-initiated clinical trials, clinical manuscript and/or grant writing is preferred