Program Specialist Salary at Napa Valley Language Academy BETA

Overview: To provide coordination and implementation support of defined tasks for the assigned program(s). Responsibilities: Schedules and coordinates both internal and external meetings. Tracks and compiles program data for program team analysis/review. Monitors program email inbox. Responds and follows up accordingly Attends program meetings and assists in follow-up with stakeholders on outstanding deliverables and action items. Assists with planning and coordination of events, conferences, and webinars, as needed. Develops and publishes agendas, meeting minutes, and necessary documentation. As directed, assists with internal and external meetings. Assists Program Manager to develop and publish communication/updates to program stakeholders. Develops and publishes stakeholder reports on defined schedule. Communicates program outcomes and potential risks to leadership Supports the successful implementation of new programs and associated processes Works with program leadership and relev

Job Description Job Description Description: The Program Coordinator works closely with the Career Specialists, providing guidance and support to the STEP-UP Program. Under the direction of the President/CEO, the Program Coordinator will audit participant files, including case reports, placement agreements, and timesheets, and provide insight as needed. The Program Coordinator will also liaise with the county to ensure participant compliance and progress throughout the STEP-UP program. The program coordinator will also ensure proper reporting, such as the All-Hours and Month-End reports, are in place. The Program Coordinator will also work alongside the Administrative Support Specialist on the Step-Up participant’s HR, onboarding, and payroll processes. Qualifications: Associate degree in an administration-related field or equivalent experience Minimum of three (3) years of experience as a supervisor in a social services or related field Experience in conducting basic needs assessments

A Bit About Us: From mosquito repellents to deodorants, Taxa is building single-application long duration skincare products, with performance measured in weeks, not hours. We aim to accomplish this by genetically engineering skin microbial species, and steering these communities away from performing undesirable metabolic functions. The Opportunity: We are seeking a Clinical Research Coordinator to join our team. A successful candidate will recruit and screen eligible research subjects, coordinate visits with participants, administer interviews, and score the responses accurately. Additionally, the coordinator will acquire and analyze research data while maintaining proper regulatory and IRB documentation throughout the study. The Clinical Research Coordinator will work closely with the entire research team to ensure the smooth and efficient execution of clinical studies. Qualifications: ✔️ 3+ cumulative years of clinical research experience. ✔️ Current work authorization in the US. ✔️

Your Role The Privacy Office develops and oversees Blue Shield’s Privacy Program. The Privacy Program ensures that Blue Shield and its affiliated covered entities, including Blue Shield of California Promise Health Plan, are in compliance with state and federal privacy laws and regulations, including the Health Insurance Portability and Accountability Act of 1996 (HIPAA), the Health Information Technology for Economic and Clinical Health Act of 2009 (HITECH), and California’s Confidentiality of Medical Information Act (CMIA). The Privacy Program Specialist, Consultant reports to the Privacy Office Manager or Director and plays an essential role in advancing and enforcing Blue Shield’s Privacy Program. Your Work In this role, you will: Be responsible for the oversight of Blue Shield's compliance with state and federal privacy laws, including HIPAA and HITECH Auditing and monitoring compliance with the Privacy Program, developing and implementing corrective action plans (CAPs) on behalf

Are you an experienced Contracts Administrator looking for a new opportunity? Our client, a leading company in the construction industry, is seeking a dedicated professional to join their team in a full-time, onsite position. As a Contracts Administrator, you will work closely with Project Managers, Estimators, and the Senior Leadership Team to ensure all projects are updated accurately, administrative duties are handled efficiently, and financials are reconciled. Key Responsibilities Provide administrative support to the projects team, including managing schedules, coordinating meetings, and handling correspondence. Maintain and organize construction-related invoices and purchase orders. Accurately input data related to construction projects, expenses, and invoices. Prepare monthly reports, including job costs, Accounts Receivable, Accounts Payable, and various cost analyses. Collaborate with Project Managers to process change order requests. Generate customer project reports and bill

VARITE is looking for a qualified Contract Management Analyst for one of its clients. WHAT THE CLIENT DOES? The company started out as a hardware/software vendor, but over time added more subscription-based services. WHAT WE DO? Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services. HERE'S WHAT YOU’LL DO: Here are the Job Details: Position: Contract Management Analyst Location: Oakland, CA, USA, 94612 Duration: 6 months Description: ONLY SUBMIT LOCAL CANDIDATES CURRENTLY RESIDING IN BAY AREA/NEAR WORK LOCATION. ASSINGMENT IS HYBRID AND ON-SITE AT OAKLAND OFFICE 2-3 TIMES PER WEEK. 3-6 MON

Job Description: We are seeking an experienced and detail-oriented Senior Study Coordinator to join our clinical research team. This role will lead the coordination and management of complex clinical trials, ensuring compliance with regulatory standards and efficient trial operations. The Senior Study Coordinator will work closely with investigators, research staff, and external partners to support high-quality, timely, and reliable data collection. Key Responsibilities: Study Coordination: Oversee multiple clinical trials, including study start-up, patient enrollment, follow-up, and study closeout, ensuring all milestones are met. Compliance and Protocol Adherence: Ensure trials are conducted in accordance with the protocol, Good Clinical Practice (GCP) guidelines, institutional policies, and applicable regulatory requirements. Data Management: Oversee the collection, entry, and management of clinical trial data, ensuring data integrity, accuracy, and timely reporting to sponsors and

Company Description Kissel Uptown Oakland, in the Unbound Collection by Hyatt, is a premier luxury hotel located in Oakland, CA. The hotel offers a sophisticated stay in 168 rooms and suites, showcasing over 9,000 SqFt of meeting and event space across four venues. Located in the vibrant Uptown area of Downtown Oakland, Kissel provides a glamorous and nostalgic experience for both locals and travelers. Role Description As a Group Rooms Coordinator, you'll be the backstage wizard, working your magic to ensure smooth and enjoyable group experiences. You'll collaborate closely with our sales team to handle everything from room blocks and reservations to VIP requests and post-stay follow-ups. Your role is pivotal in creating memorable moments for our guests, from the moment they inquire to the time they check out. Your Duties, Your Magic: Curate the Perfect Stay: Craft bespoke group packages, tailoring them to each client's unique needs. Master the Room Block: Juggle room blocks with fines