Collecting information
Organizing data
You will report directly to the Executive Director, Administrator, or Senior Patient Care Manager.. At least three years’ experience of direct patient care and two years’ experience in hospice or home-based care setting. Demonstrates knowledge and compliance with accepted hospice principles and practice, including industry standards, regulations, and best practices (i.e., Medicare, Medicaid, JCAHO, ACHC), company policies/procedures, and understanding of terminally ill patients and their families. Ability to apply knowledge of the unique needs of hospice patient and families from various socioeconomic backgrounds to provide appropriate advocacy and oversight. Comprehensive Benefits Package: Health Insurance, 401k Plan, Tuition Reimbursement, PTO
Gentiva Hospice is a member of the Gentiva family – an industry leader in hospice, palliative, home health, and personal home care. We're looking for a RN Patient Care Manager to join our team. You will report directly to the Executive Director, Administrator, or Senior Patient Care Manager. Managing the site in the absence of the Executive Director, Administrator, or Senior/Executive Patient Care Manager. Knowledge of terminally ill patients and their families along with understanding of hospice concept; knowledge of roles of all disciplines providing hospice services; excellent patient assessment skills; good oral and written communication; thorough knowledge of managed care principles, regulatory guidelines (i.e., Medicare, Medicaid, and human resource) management principles.
Step into a high-impact leadership role at a nationally affiliated cancer center driving innovation in oncology research.. MD Anderson Cancer Center at Cooper seeks a Medical Oncologist to serve as Director of Research& Clinical Trials, expanding an established program and launching a new Phase 1 site.. Strengthen collaboration with MD Anderson Cancer Center in Houston on joint research initiatives. The Camden Waterfront features major attractions, including the Adventure Aquarium and Battleship New Jersey. Internal Medicine, Hematologist Oncologist, Ho, Hematology Oncologist, Oncology, Oncologist, Blood, Blood Illness, Blood Cells, Physician, Healthcare, Health Care, Patient Care, Hospital, Medical, Doctor, Md
Heartland Hospice is a member of the Gentiva family - an industry leader in hospice, palliative, home health, and personal home care.. You will report directly to the Executive Director, Administrator, or Senior Patient Care Manager.. At least three years’ experience of direct patient care and two years’ experience in hospice or home-based care setting. Demonstrates knowledge and compliance with accepted hospice principles and practice, including industry standards, regulations, and best practices (i.e., Medicare, Medicaid, JCAHO, ACHC), company policies/procedures, and understanding ofterminally ill patients and their families. Company: Heartland Hospice
The Clinical Research Nurse, ensures that the health and safety of research participants and the integrity and quality of clinical trials, are maintained and conducted in accordance with federal, state, IRB, departmental, and institutional regulations, policies and procedures. The Clinical Research Nurse will primarily provide nursing expertise and care to research study patient management with primary focus on bone marrow transplantation and cellular therapy clinical trial protocols. They will serve as a liaison and work closely with investigators, department members, study sponsors, IRB and the institution, to support administration of compliance, financial, personnel and other related aspects of all ongoing clinical studies. Minimum 2 years’ experience in Pediatric Bone Marrow Transplant/Hematology-Oncology nursing required.. Knowledge of Institutional Review Board (IRB) policies and procedures
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.
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.
Learns, understands and becomes proficient in relevant facility, Dignity Health and external data sources and systems including, but not limited to, clinical process and outcome data, electronic health record data, event reporting data, and patient complaints, etc. e.g. Midas+, iVOS, ATLAS, etc.. Prior experience with Cerner, Epic, Meditech, Allscripts, and Midas is a plus.. Working knowledge of National Quality Forum (NQF), Agency for Healthcare Research and Quality (AHRQ), Institutes for Healthcare Improvement (IHI) safety indicators, serious reporting events, safe medical practices, and Centers for Medicare and Medicaid Services (CMS) quality measures helpful. Specializing in cardiovascular care, comprehensive cancer services, and women and children's services, including neonatal intensive care, St. Joseph's is the largest hospital, as well as the largest private employer, in Stockton, California.
The GRA Device team is a globally diverse team supporting the medical device, combination product, biosurgery, digital health and in-vitro diagnostic products within the Sanofi portfolio of products.. The team is part of the Global Regulatory Affairs, Regulatory CMC and Device Department within Global Research and Development.. Contribute to product development planning, including strategies to bridge drug delivery systems during development. Proven experience in global medical devices regulatory for drug-led combination products and standalone drug delivery devices. Working knowledge with technical/industry standards related to combination products and standalone drug delivery medical devices
As a Clinical Research Monitor, you ensure trial patients' safety by assuring trials are conducted ethically and within regulatory compliance, data accuracy, and protocol adherence.. Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements.. Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Boards, Contract, and Training, developing process improvements.. 3 year's relative work experience in the areas of clinical research (as a CRC or CRA) including quality assurance/control and regulatory compliance or field monitoring. Understanding of cardiovascular anatomy, pathology and physiology
Must hold appropriate credential, including one or more of the following: Certified Clinical Research Professional (CCRP), Certified Clinical Research Associate (CCRA), Masters in Public Health, Masters in Clinical Research, Masters in Clinical Trials, Masters in Research Administration, Master of Healthcare Administration, or similar qualification.. Pursuant to the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act (Clery Act), you may view Portland Community College’s (PCC) most recent Annual Security Report (ASR) on the Department of Public Safety website.. The ASR contains current security and safety-related policy disclosure statements, emergency preparedness and evacuation information, crime prevention and sexual assault prevention information and resources, and drug and alcohol prevention programming.. The ASR also contains crime statistics for Clery Act crimes which occurred on PCC properties for the last three calendar years.. Paper copies of the ASR are available upon request at all Department of Public Safety offices.
We are seeking a Sr. Research Nurse who will provide research coordination support for complex early phase clinical trials conducted in the Drug Development Unit (DDU) in the Division of Clinical Pharmacology.. The Sr. Research Nurse will collaborate with the study's clinical team and faculty to implement multiple research protocols and will oversee study related activities.. Oversees and supports study visits for non-licensed DDU staff (e.g. study coordinator, clinical research fellow).. At the direction of the Clinical Pharmacology faculty, assists in ordering research doses of radioisotopes from a commercial radiopharmacy.. Assist in monitoring the data integrity of studies assigned to other research nurse coordinators using Quality Assurance forms maintained by the DDU.
As a Data Integration Lead - Medicaid/Medicare Technologies at Gainwell, you can contribute your skills as we harness the power of technology to help our clients improve the health and well-being of the members they serve — a community’s most vulnerable.. Conducts technical research, testing, evaluation and documentation of moderately complex hosting/configuration tools and methodologies to ensure that tools are current and functional.. Nine or more years of SSIS, Webservices, AWS Glue, and SQL, with experience working with Medicaid and Medicare technologies.. A strong foundation in software and product design methodologies, programming languages, operating systems, web development and application implementation across the development life cycle.. Remote work within the United States.
Collaborates with Cancer Center nursing staff to provide nursing care to patients receiving therapy on a clinical research trial.. Coordinate study enrollment, protocol treatment and follow up care for patients participating in clinical trials.. Provides patient teaching about research in general, their specific clinical trial and treatment they will be receiving, HIPAA regulations and any other information related to clinical trials.. Prepares and submits clinical trial information for IRB submission and presents to IRB with PI. Gives required updates and summary.. Maintains NCI RCR investigator registrations and other relative research compliance documentation.
QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology, mechanistic PK-PD modeling and pharmacometrics of oncology drugs from post-PCC to registration.. Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics (monoclonal antibodies, antibody drug conjugates, T-cell engagers, bispecifics) in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications (CTDs. Ph. D., with at least seven years of pharmaceutical drug development experience relating to: systems biology, PKPD, pharmacometrics, mathematics, chemical/biomedical engineering or related field.. Antibody Drug Conjugates (ADC), Clinical Pharmacology, Data Modeling, Data Modeling Software, Data Modeling Tools, Data Visualization, Drug Development, Pharmacology Research, Pharmacometrics, Regulatory Documents. C (Programming Language), Clinical Trials, MathWorks SimBiology, MATLAB, Nonlinear Mixed Effects Modeling (NONMEM), NONMEM, Oncology, Pharmaceutical Development, PKPD Modeling, Programming Languages, Regulatory Submissions, R Programming, T Cells
Part-time Assistant Clinical Research Coordinator. The Helen Diller Family Comprehensive Cancer Center (HDFCCC) Clinical Research Support Office (CRSO) has experienced unprecedented growth in the recent years and is seeking a limited appointment Assistant Clinical Research Coordinator for the Pediatric Oncology Program to assist with the daily needs of our clinical trials.. The HDFCCC integrates the work of researchers and clinicians dedicated to four fundamental pursuits: laboratory research into the causes of cancer progression; clinical research to translate new knowledge into viable treatments; compassionate, state-of-the-art patient care; and population research that can lead to improvements in prevention, early detection, and quality-of-life for those living with cancer.. The twin pillars of precision medicine and precision population health guide research and treatment at HDFCCC.. The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.
(e.g. Midas+, iVOS, ATLAS, etc. Prior experience with Cerner, Epic, Meditech, Allscripts, and Midas is a plus. Working knowledge of National Quality Forum (NQF), Agency for Healthcare Research and Quality (AHRQ), Institutes for Healthcare Improvement (IHI) safety indicators, serious reporting events, safe medical practices, and Centers for Medicare and Medicaid Services (CMS) quality measures helpful.. St. Joseph's Medical Center was founded in 1899 under the direction of the Dominican Sisters of San Rafael and is a not-for-profit, fully-accredited regional hospital with 395 beds, a physician staff of over 400 and more than 2400 employees.. Specializing in cardiovascular care, comprehensive cancer services, and women and children's services, including neonatal intensive care, St. Joseph's is the largest hospital, as well as the largest private employer, in Stockton, California.
Working Title: Clinical Research Coordinator. Collaborate with other clinical research team members, investigators, and hospital staff to ensure tests and procedures required by research protocols are performed and documented (e.g., vital signs, phlebotomy, specimen processing, electrocardiograms (EKGs), research drug administration, and protocol-specific tests and procedures); follow up with appropriate persons on missing or discrepant data. ECO Pass: Reduced rate RTD Bus and light rail service. CCRC - Certified Clinical Research Coordinator. CCRA - Certified Clinical Research Associate
As an essential healthcare system, Harris Health champions better health for the entire community, with a focus on low-income uninsured and underinsured patients, through acute and primary care, wellness, disease management and population health services.. Ben Taub Hospital (Level 1 Trauma Center) and Lyndon B. Johnson Hospital (Level 3 Trauma Center) anchor Harris Health’s robust network of 39 clinics, health centers, specialty locations and virtual (telemedicine) technology.. The D PS/RM serves as the liaison between the system and hospital executive team for matters related to the Patient Safety or Risk Management program.. The D PS/RM reports directly to the Vice President of Patient Safety and Risk Management with a dotted line to the pavilion Executive Vice President (EVP).. - Certified Professional Patient Safety (CPPS) (Or) Cert Prof-Healthcare Risk Management (CPHRM) (Or) Cert Prof in Health Care Quality (CPHQ) within 2 years of employment
The Clinical Research Director (CRD), Immunology & Inflammation (I&I) Therapeutic Area is responsible for the creation of the clinical development plan in alignment with the project strategy, its endorsement by governance and its execution in close collaboration with clinical operations.. Create the clinical development strategy for one or more assets and document it in the clinical development plan in collaboration with the global project team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, drug safety, marketing.. Contribute to data review, interpretation and publication of clinical study results.. Have an understanding of novel biomarker and precision medicine approaches, novel clinical trial designs, endpoints and statistical methods.. Should be board certified or equivalent in dermatology or allergy/immunology.