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Cedars-Sinai is seeking a Clinical Research Finance Coordinator II (Pre-Award) to join our dynamic research team.. The Clinical Research Budget Coordinator II develops complex clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research.. Develops complex clinical trial budgets for industry and the National Institutes of Health (NIH) as well as investigator-initiated clinical research.. Performs Medicare coverage analysis for clinical trials and collaborates with Institutional Review Board (IRB) to finalize and obtain approval.. Business Entity : Cedars-Sinai Medical Center
Supervisor of Nursing Clinical Research (RN) at Providence Saint John's Cancer Institute in Santa Monica, CA. This position will oversee clinical trials at the Cancer Institute and will not directly supervisor employees. Saint John’s Cancer Institute (SJCI) is a pioneer in drug discovery, therapeutics, clinical trials, and research. The Sisters of Providence and Sisters of St. Joseph of Orange have deep roots in California, bringing health care and education to communities from the redwood forests to the beach shores of Orange county - and everywhere in between. In Southern California, Providence provides care throughout Los Angeles County, Orange County, High Desert and beyond. Category:Science, Keywords:Clinical Research Associate (CRA), Location:Inglewood, C90311
Job Summary: Patient Safety Officer RN in acute care hospital setting.. You will attend national safety goal monitoring committees, sit on nursing committees such as falls and medication safety, conduct chart reviews and need to be good at root cause analysis and work with CDPH adverse patient event criteria for reporting.. In addition to the responsibilities listed above, this position is responsible for developing patient safety programs and initiatives by developing and monitoring the procedures for reporting safety hazards, accidents, incidents, threats, significant events, in line with best practices; and developing and revising patient strategies based on patient outcomes and leads improvement activities for patient care and operational programs which aim to improve outcomes.. Listens, responds to, seeks, and addresses performance feedback; provides actionable feedback to others, including upward feedback to leadership and mentors junior team members.. Recognizes and capitalizes on improvement opportunities; evaluates recommendations made; influences the completion of project tasks by others.
Our client, a provider of Health, Dental, Vision, Medicaid, and Medicare Healthcare service plans in the state of California with 4.7 million members and $22.9 billion of annual revenues , seeks an accomplished Medicare Enrollment Coordinator.. We’re seeking Bilingual (Spanish-English) Medicare Enrollment & Sales Support Coordinators to join our Medicare Sales Team during the Annual Enrollment Period (AEP).. Must have Ethernet connection for remote work – equipment provided.. Answer and triage incoming calls from prospective members, directing non-sales calls appropriately.. Collaborate with other departments (Medicare Outreach, Billing, Customer Care) to resolve member inquiries.
At CHOC, we strive to be the leading destination of children's health by providing exceptional and innovative care.. CHOC's compensation structure, benefits offerings, and career development programs are geared to helping you achieve your professional and personal goals.. The Coordinator of Regulatory Affairs assists with ensuring compliance with all relevant healthcare regulations and standards including the Joint Commission (TJC), the California Department of Public Health (CDPH), the Centers for Medicare and Medicaid Services (CMS), and other regulatory agencies for Children's Hospital of Orange County (CHOC) healthcare facilities including CHOC Orange and CHOC at Mission Hospital.. CHOC does not discriminate on the basis of age, race, color, religion, national origin, ancestry, marital status, genetic information, disability, sex, gender (including pregnancy, breastfeeding, childbirth, lactation or related medical conditions), gender identity or expression, medical condition, sexual orientation, veteran status, military or uniformed service member status, or other protected characteristics in accordance with state and federal laws.. CHOC will consider for employment qualified applicants with criminal histories, in accordance with the Fair Chance Initiative for Hiring.
destinationone Consulting specializes in recruitment across diverse sectors, including Healthcare, Health Tech, Government, Municipalities, Non-Profits, Legal, Public Accounting, Food and more.. The Quality Assurance Coordinator is responsible for monitoring and evaluating the quality of care provided within the healthcare practice, ensuring that standards are met and continuously improved.. Bachelor's degree in Healthcare Administration, Nursing, or a related field; certification in quality management preferred.. Experience in quality assurance or improvement in a healthcare setting.. Disclaimer: We're proactively building a databank for opportunities in Healthcare, Health Tech, Government, Non-Profits, Legal, and more.
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects' (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities.. The CRC-II is the mid-level position in the Clinical Research Coordinator series.. Association of Clinical Research Professionals Certified Professional (ACRP-CP), Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC).. Airborn Communicable Disease, Bloodborne Pathogens, Chemical, Dust Particular Matter, Extreme Noise Levels, Extreme Temperatures, Radiation, Uneven Surfaces or Elevations. CHOC does not discriminate on the basis of age, race, color, religion, national origin, ancestry, marital status, genetic information, disability, sex, gender (including pregnancy, breastfeeding, childbirth, lactation or related medical conditions), gender identity or expression, medical condition, sexual orientation, veteran status, military or uniformed service member status, or other protected characteristics in accordance with state and federal laws.
Oversee the development and finalization of high-quality, scientifically accurate, ICH-compliant documents, including clinical study protocols and reports, Investigator Brochures, Periodic Safety Updates, patient narratives, and manuscripts for peer-reviewed publications.. 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.. Deep understanding of ICH-GCP guidelines and other relevant regulatory requirements.
Join our dedicated team as a Clinical Research Nurse specializing in cancer research!. Under the direction of the Cancer Research Manager, you will play a vital role in executing protocol-specific research activities.. You will ensure that all research activities are in compliance with ICH Good Clinical Practice Guidelines, IRB policies, and all relevant state and federal regulatory requirements.. Collaborating with a multidisciplinary team and research department staff, you will help ensure high-quality research and support patients in navigating the complexities of clinical trials and hospital systems.. At least 1 year of experience with Oncology Clinical Trials (both Sponsor and Cooperative Group).
Manages the Plan’s Provider Contracting functions and team members.. Implements cost control initiatives to positively influence the Medical Care Ratio (MCR) in each contracted region.. Develops and implements contracting strategies to comply with state, federal, NCQA, HEDIS initiatives and regulations.. 7+ years' experience in Healthcare Administration, Managed Care, Provider Contracting and/or Provider Services, including 2+ years in a direct or matrix leadership position. Working experience with, and strong knowledge of, various managed healthcare provider compensation and VBP methodologies, primarily across Medicaid and Medicare lines of business, including but not limited to; fee-for service, capitation and various forms of risk, ASO, etc.
Director, Regulatory Affairs - Regulatory Operations and North America. Director, Regulatory Affairs - Regulatory Operations North America. As the Director, Regulatory Affairs, Regulatory Operations and North America for Advanced Bionics, you will play a critical leadership role in guiding the regulatory team in navigating complex regulatory landscapes and ensuring compliance with all applicable regulations of active implantable medical devices.. Compliance Oversight: Ensure that the company's products comply with regulatory standards (FDA, EU MDR, and other international regulations) throughout the product lifecycle.. In conjunction with Clinical Research, prepare or direct regulatory affairs staff in the generation of applications (i.e., IDE) for conducting clinical investigations.
Director, Regulatory Affairs - Regulatory Operations and North America 158789. Director, Regulatory Affairs – Regulatory Operations North America. As the Director, Regulatory Affairs, Regulatory Operations and North America for Advanced Bionics, you will play a critical leadership role in guiding the regulatory team in navigating complex regulatory landscapes and ensuring compliance with all applicable regulations of active implantable medical devices.. Compliance Oversight: Ensure that the company's products comply with regulatory standards (FDA, EU MDR, and other international regulations) throughout the product lifecycle.. In conjunction with Clinical Research, prepare or direct regulatory affairs staff in the generation of applications (i.e., IDE) for conducting clinical investigations.
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
Director Regulatory Affairs Regulatory Operations North America. As the Director Regulatory Affairs Regulatory Operations and North America for Advanced Bionics you will play a critical leadership role in guiding the regulatory team in navigating complex regulatory landscapes and ensuring compliance with all applicable regulations of active implantable medical devices.. Compliance Oversight : Ensure that the companys products comply with regulatory standards (FDA EU MDR and other international regulations) throughout the product lifecycle.. Submissions and Approvals : Lead the preparation submission and maintenance of regulatory filings for the US and conjunction with Clinical Research prepare or direct regulatory affairs staff in the generation of applications (i.e. IDE) for conducting clinical investigations.. Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills
Placing Intravenous catheters, completing blood draws from established lines, numbing venous sites, medical histories, post care medical instructions, and assisting in emergency medical administration (minimum requirement registered nurse/ a licensed vocational nurse may perform some of these duties).. May assist with monitoring safety reviews, protocol deviations, device deficiencies and adverse event reporting for investigational medical devices to assure adherence to Good Clinical Practices (GCP), FDA and MDD regulations.. Position Levels (Commensurate with education, skillset, experience and level of responsibilities, years of experience are indicated as a general guideline and are not mandatory): Clinical Research Lab RN I. Clinical Research Lab RN Supervisor. Experience in Post Market surveillance of Medical Devices and Regulatory Affairs submissions for new or modified devices desirable
UCan do all this and more at UCLA Health.. Experience using online payer sites with the ability to check claim status, denials, and eligibility. Knowledge of CPT, ICD-10, and HCPC codes. UCLA Health is a world-renowned health system with four award-winning hospitals and dozens of primary care practices, specialty practices, urgent care centers and other ancillary locations throughout metro Los Angeles as well as the David Geffen School of Medicine.. If you're looking to experience greater challenge and fulfillment in your career, you can at UCLA Health.
The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot.. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs.. Is part of the California Institute for Regenerative Medicine (CIRM) Alpha Stem Cell Clinic network. The Regulatory Affairs Manager, under the general direction of the Assistant Director, will serve as a senior-level expert in clinical research protocols and regulatory processes within the Alpha Clinic.. The Regulatory Affairs Manager applies extensive knowledge of clinical research protocols and processes to design research projects of large scope and high degrees of complexity.
ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.. Lead/moderate DSMB teleconferences, monthly PI and Study Coordinator teleconferences.. Bachelor's degree in biological science with 5+ years of relevant experience in clinical research required. Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks. Exempt Employees are eligible for Unlimited PTO *