Legal Assistant Salary at Buckley & Zopf BETA

Overview Responsible to coordinate activities surrounding the quality program within the solid-organ transplant program. Develops and implements quality system measures of key activities with the transplant program for purposes of maintaining regulatory compliance with the Centers for Medicare & Medicaid Services (CMS) and the United Network of Organ Sharing (UNOS). Responsibilities Maintains CMC and UNOS program compliance by identifying and communicating required regulations and compliance. Coordinates the program's quality assurance/process improvement program. Collects and reviews program data on a regular basis and makes decisions/ recommendations to leadership regarding program improvements. Prepares and reports out on program quality and volume metrics from UNOS and SRTR (Scientific Registry of Transplant Recipients) to leadership, regulatory agencies and insurance payers as required. Collects and analyzes program and patient data for maintaining quality measures. Prepares and m

Overview SIGN ON BONUS ELIGIBLE - Orthopaedics The Clinical Research Coordinator III performs a full range of clinical research duties at an advanced level and plans, organizes, leads, and performs comprehensive clinical trial duties for multiple or complex clinical trials, focusing on the overall productivity and success of the program. The expectation is to perform with limited supervision and actively participate in decisions regarding the clinical research process, often leading teams. The impact of decisions of the Clinical Research Coordinator III are wide in scope affecting both internal and external partners. They cannot perform any tasks that by state or local law require a license to perform. Responsibilities * * Research Operations- Occasionally requiring tasks outside of defined operating hours: * Mentors, onboards, trains and oversees new clinical research coordinator staff onGood Clinical Practice (GCP), Human Subjects Protection (HSP) practices,the ethical conduct of res

Overview Onsite - 40 hours/week : Dartmouth Cancer Center Coordinates and/or manages all aspects of complex, multi-component research projects, general research and projects for the assigned service line. Manages activities related to regulatory compliance and staff training, project contracts, budgets, and all related research finances, workforce needs throughout the research group, maintenance of databases and coordination with the Office of Sponsored Projects for any state or federally funded studies. Provides oversight of any project that requires a filing with national boards or committees (i.e., Institutional Research Board (IRB)/ Committee for Protection of Human Subjects (CPHS), etc.), and assures compliance with the Food and Drug Administration (FDA), Good Clinical Practice (GCP) research standards, JCAHO and Internal Conference on Harmonization (ICH) guidelines as appropriate. Provides a forum for review and vetting of new protocols and the progress of existing protocols and

Overview Provides leadership, support, and guidance for medication management areas within the Dartmouth Health (DH) system. Responsible for coordinating with leadership on the development, implementation and monitoring of the inpatient, retail, and ambulatory space with respect to adherence to medication regulatory compliance, quality improvement, and patient safety. Organizes and leads policy and procedure review and development, manages quality assurance and process improvement projects, assists with accreditation/reaccreditation, and ensures compliance with regulatory, accrediting agencies and any internal and external audits. Facilitates and leads meetings comprised of representatives from various departments across DH sites to create productivity and quality/safety measures, monitor trends, and develops action plans to achieve the highest quality, productivity and compliant/safe practices. Responsible for ongoing tracking of implemented standards from regulatory and accreditation

Overview Monday - Friday 7:30 - 4pm Responsible for oversight and management of all distribution activities and functions, to include maintaining the inventory integrity of the supplies stocked in the central warehouse and throughout all D-HH sites. Responsibilities * Inventory Management: * Conducts all aspects of ordering, receiving, distribution, and warehousing of essential supplies across D-H system locations. * Maintains and strives to continuously improve inventory systems to order, control, and stat/expedite supplies to enhance the fiscal management of the department. * Adjusts item re-ordering points based on EOQ/TOC methodology. * Assists in resolving inventory, product and stock issues as well as shipping and receiving issues directly with Supply Chain team. * Leads cycle counts and annual physical inventory to verify accuracy and resolve product discrepancies, working with Supply Chain Technology to update system * Collaborates with Supply Chain Management and system member

Overview Directs and coordinates the administrative, financial, regulatory, compliance and marketing activities of the transplant services. Assumes responsibility for the overall administrative supervision of services delivered to all kidney, kidney-pancreas and pancreas transplant patients; and the development of departmental policies and procedures, standards of practice and performance improvement activities. Responsibilities * Develops and oversees the section and transplant program budgets. * Assumes responsibility for the oversight and management of the organ acquisition portion of the Medicare cost report; including ensuring systems and processes are in place to maximize the costs captured while remaining in compliance with Medicare guidelines. * Assumes responsibility for the oversight and management of contracts with our various payers including involvement in the updating and negotiating of these contracts, identification of new networks, development of strategic relationship

**_What Commercial Transaction contributes to Cardinal Health_** The Legal function provides the company with strategic, proactive, practical and cost-effective legal advice and services in order to protect the organization's assets, operations and image. This function provides legal counsel related to commercial, corporate securities, intellectual property, labor and employment, and regulatory law, among other areas. This function also litigates all company legal matters, manages outside counsel and manages legal operations. Commercial Transaction attorneys provide legal advice, counsel and services to domestic and international businesses in support of customer, vendor, supplier, and strategic relationships, including drafting and negotiating contracts, participating in and providing input on business strategy, and otherwise acting as primary day-to-day legal contacts for business clients. **_Job Summary_** The Senior Legal Counsel, serves as the primary legal partner to leaders of a

Posting date: 03/10/2025 Open Until Filled: Yes Position Number: 0027900 Position Title: Assistant Vice President for Finance & Controller Hiring Range Minimum: Please Inquire. Hiring Range Maximum: Please Inquire. Union Type: Not a Union Position SEIU Level: Not an SEIU Position FLSA Status: Exempt Employment Category: Regular Full Time Scheduled Months per Year: 12 Scheduled Hours per Week: 40 Schedule: M-F 8:00AM-5:00PM Location of Position: Hanover, NH Remote Work Eligibility?: Hybrid Is this a term position?: No Is this a grant funded position?: No Position Purpose: The Assistant Vice President for Finance & Controller collaborates with the CFO to initiate and lead division-wide activities for the Finance division and serves as the accounting expert for the institution. Leads the design, development, and oversight of critical institutional policies, procedures, and systems associated with the management of Dartmouths financial resources and business operations. Oversees centralize