Collecting information
Organizing data
Prepare, review, and analyze SNF, Home Health & Hospice Medicare and Medicaid cost reports in accordance with Federal and State regulations.. 5+ years of experience in post- acute healthcare reimbursement including Medicare, Medicaid and cost reporting.. At Plante Moran, diversity, equity and inclusion means that all staff members have equitable and fair opportunities to succeed, in an inclusive environment, with their individual, unique identities. We believe that face-to-face interactions are paramount for individual and collective development, but also encourage individuals to work with their supervisor and team to determine their optimal working environment each day. A Pension plan is also available for eligible administrative and paraprofessional staff.
Prepare, review, and analyze SNF, Home Health & Hospice Medicare and Medicaid cost reports in accordance with Federal and State regulations. 5+ years of experience in post- acute healthcare reimbursement including Medicare, Medicaid and cost reporting. At Plante Moran, diversity, equity and inclusion means that all staff members have equitable and fair opportunities to succeed, in an inclusive environment, with their individual, unique identities.. We believe that face-to-face interactions are paramount for individual and collective development, but also encourage individuals to work with their supervisor and team to determine their optimal working environment each day.. A Pension plan is also available for eligible administrative and paraprofessional staff.
Job Description & Requirements Chicago, IL - Medical Oncologist StartDate: ASAP Pay Rate: $530000.00 - $550000.00 Medicine Medical Group seeks an exceptional Medical Oncologist to join a growing practice of experienced medical oncologists in Tinley Park, IL. Medical Oncologist Physician Roles and Responsibilities.. Exceptional benefits – Medical, dental, retirement, time off, and CME allowance Community Information—Live and work in Chicago!. The third-largest city in the nation, Chicago is filled with excitement and sought-after attractions, including Buckingham Fountain, Millennium Park, and many more of the city’s well-known distinctions.. Along with its superb medical facilities, visitors to Chicago relish the city’s 29-mile long lakefront park, fabulous shopping districts, multicultural neighborhoods and world-class arts and entertainment.. Internal Medicine, Medical Oncology, Chemotherapy, Hormonal Therapy, Biological Therapy, Cancer, Md
The Director will work with the broader quality unit and technical operations departments (product development and commercial manufacturing) to maintain and improve the overall Product Quality Management Program, including developing a clear mission and vision for supplier quality management (SQM) and providing quality assurance oversight of product related changes, deviations and complaint investigations, batch review and release, technology transfer and process validation.. Manage Product Quality SQM standards including: supplier identification and selection; supplier evaluation and approval; supplier quality agreements; supplier performance monitoring and supplier relationship management.. Work with the Regulatory Affairs and Quality Unit departments in facility Heath Authority Inspections.. Provide quality oversight and support to technology transfer, process validation and product risk management. 8-10+ years in quality, compliance, and pharmaceutical supplier quality management, including GXP facility audits, in a regulatory environment (FDA, MHRA, Notified Body, etc) required
Business Unit: Rush Bone Marrow Transplant and Cell Therapy Center. Exemplifies the Rush mission, vision and ICARE values and acts in accordance with Rush policies and procedures.. Chief Nursing Officer must provide approval for any RNs with ADN degree hired after 10/22/2020, based upon unit need.. ADN RNs hired after 10/22/2020 must show continued enrolment towards a BSN degree with a signature of contract stipulating a BSN degree must be completed within 3 years of hire, Failure to do so will result in termination.. Provides nursing care to patients participating in clinical research studies, may include: standard of care procedures, research procedures, study medication administration and adherence assessments, adverse event assessment documentation, blood draw, EKG administration, and various clinical assessments.
With an independent, National Cancer Institute-designated comprehensive cancer center that is ranked top 5 in the nation for cancer care by U.S. News & World Report at its core, City of Hope’s uniquely integrated model spans cancer care, research and development, academics and training, and a broad philanthropy program that powers its work.. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and cancer treatment centers and outpatient facilities in the Atlanta, Chicago and Phoenix areas.. Under direct supervision of their Clinical Research leader, the incumbent is responsible for supporting clinical trials at the top of their nursing license scope, for existing and novel oncology therapies while working in a fast-paced environment.. The CRN assists clinicians (LPNs, MAs, and/or RNs) as needed to ensure that protocol- required specimen collections, electrocardiograms, vital signs, study drugs and customary usual care medications, IV start and IV discontinuation as well as follow-up observations are performed per protocol (as applicable).. The Clinical Research Nurse will provide consistent oversight to ensure competent and standardized practices and coordinate strategies to enhance departmental communication and collaboration.
We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio.. Responsible for quality of assigned Biological, Neurotoxin and/or Gene Therapy products to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide.. Acts as the primary quality representative for the global supply chain pertaining to external manufacturing business relationships and builds and maintains relationships with TPM Operations, Supplier Quality Management, TPM Business Alliance, Commercial, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs, R&D, and PDS&T to ensure alignment. Develops Global Product Quality Assurance strategy and implements agreed strategy to support pharmaceuticals, Biologics, Neurotoxin and/or Gene Therapy produced at AbbVie plants as well as third party manufacturing (TPM) facilities.. Minimum of 10+ in Quality Assurance Operations Management, Regulatory, Operations, or Technical Support in a pharmaceutical setting.
They are seeking a Clinical Research Coordinator (CRC) responsible for coordinating and managing clinical trials and research studies in accordance with regulatory requirements, study protocols, and institutional policies.. The CRC will work closely with investigators, sponsors, and study participants to ensure the ethical and accurate collection of data and the integrity of the research process.. Coordinate day-to-day clinical trial activities and ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory guidelines.. Knowledge of clinical research regulations and GCP.. Experience with IRB submissions and sponsor communications.
Provides strategic leadership and management of department overseeing compliance with regulations and laws related to Risk Adjustment across our Marketplace, Medicaid and Medicare lines of business, which includes implementation of elements of an effective compliance program. Participates in mock and actual CMS and other regulatory audits and coordinates with Internal Audit, Regulatory Compliance and/or Market based Regulatory Affairs on responses to agency inquiries and oversees the internal and external processes required to ensure the Company maintains a consistent state of Audit readiness. Master's Degree CPA, CISA, JD, MHA, MBA, MIS or equivalent experience preferred.. 4+ years’ Experience with risk adjustment processes, procedures, and oversight of same preferred.. Qualified applicants with arrest or conviction records will be considered in accordance with the LA County Ordinance and the California Fair Chance Act
At Northwestern Medicine, we pride ourselves on providing competitive benefits: from tuition reimbursement and loan forgiveness to 401(k) matching and lifecycle benefits, we take care of our employees.. The Clinical Research Nurse Coordinator reflects the mission, vision, and values of NM, adheres to the organization's Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.. The Clinical Research Nurse Coordinator is a registered professional nurse who demonstrates exemplary clinical research knowledge, has strong communication skills and is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams (e.g., investigator initiated trials, sponsor trials) and Northwestern Medicine; a joint collaboration between NMG and the NU Feinberg School of Medicine.. The Clinical Research Nurse Coordinator (CRNC) works collaboratively with the inter-professional team and peers to ensure appropriate implementation and conduct of clinical research studies throughout the lifecycle of a protocol.. The CRNC utilizes the NIH Clinical Research Nurse Domain of Practice and Model of Care.
No other company in the world helps more people share professional knowledge or make business connections. Knowledge of API testing using tools like Postman.. Strong wellbeing support through EAP assistance, mental health first aiders, free access to a wellness app and more.. Quality Assurance Manager, RWE Clinical Trials (Remote).. Analyst - Quality Assurance Financial Crime ComplianceSenior QA Engineer, Secure Remote Access TestingAnalyst - Quality Assurance Financial Crime ComplianceSr. Program Manager, Quality Assurance/Regulatory Affairs (Hybrid)
Join to apply for the Inventory Control & Quality Assurance Manager (Food Industry) role at Conexus Food Solutions. Conexus Food Solutions is a leader in the Asian food service industry, bringing a diverse range of ethnic cuisines, such as Chinese, Japanese, Korean, and Thai, to the table.. Quality Assurance Manager - Steel Manufacturing. Director, Food Safety and Quality Assurance - Buckhead ChicagoQuality Assurance and Regulatory Affairs Manager. Quality Assurance Manager, RWE Clinical Trials (Remote)
Cardiosense's solutions are built on over a decade of clinical research and we continue to collaborate with the world's leading academic institutions to introduce the next generation of cardiac monitoring and disease management.. Work closely with data science and product teams to define clinical data requirements for AI model validation.. Minimum 8-10 years of experience in clinical research, with at least 5 years in a leadership role managing clinical trials, preferably in the medical device, digital health, or AI/healthcare sectors.. Proven experience designing and executing clinical studies, including model validation trials, for medical AI or digital health products.. Familiarity with AI model validation methodologies, particularly in healthcare applications.
Bachelor's degree in a Scientific, Engineering, Computer Science, or other core Life Science discipline, or a combination of training and experience demonstrating the equivalent.. A minimum of 6 years combined work experience in heavily regulated fields such as medical devices, pharmaceuticals, or biologics.. Advanced degree in scientific, technology or regulatory affairs disciplines.. Regulatory Affairs Certification (RAC) issued by the Regulatory Affairs Professionals Society (RAPS).. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI).
Clinical Research Nurse - Where Science Meets Purpose. As one of the nation's most respected infertility treatment centers, we've been helping people build families in the Chicagoland area for over 30 years.. 25,000+ IVF procedures - the most in the Midwest. We're seeking a full-time Clinical Research Nurse to join our River North team and support our ongoing clinical trials.. 3+ years of clinical research experience (IRB/GCP/FDA compliance required)