Reporting Specialist Salary at Experian Us BETA

Title: Regulatory Affairs Specialist Reports to: VP of Quality & Regulatory Affairs Location: Remote initially then transitions to on-site (Irvine, CA office) Salary Range: $110,000 - $120,000 per year Local candidates only; no relocation will be provided for this position. The Kardion Regulatory Affairs team is seeking a high energy, driven individual who is looking for the unique opportunity and challenge provided by a clinical stage startup. You will join a small team who left great jobs to go “all in” with Kardion to bring a great product that they passionately believe in to market. Communication skills, humility, competitive spirit and team fit are paramount. The Regulatory Affairs Specialist is a key partner within Regulatory Affairs and will have responsibility of the direct execution of some corporate regulatory filings. This role will work independently on some submissions and partner with others in the Regulatory Team on other US FDA filings, including IDEs, 510(k)s and PMA.

Kahana Feld is a nationally recognized, award-winning law firm with twelve offices across the country-and we're continuing to expand our team Summary The Paralegal will be responsible for working with attorneys and other departments and/or staff as assigned to provide support through all aspects of litigation in a variety of practice areas. Duties and Responsibilities: Under the supervision of an attorney, coordinate, organize, prepare, and interpret complex legal documents. Coordinate with attorneys and paralegal Is to direct workflow on various cases. Supervise paralegal Is on their duties performed and assist accordingly. Review and maintain documents and case files ensuring accuracy, organization, and confidentiality Compile pleadings for filing with courts and relevant agencies. Conduct electronic document reviews, coordinate productions of documents with attorneys, conduct searches of production databases for relevant documents, and conduct other related eDiscovery tasks. Assist

Job Description Job Description Summary: The successful candidate will be responsible for the design and maintenance of MPM financial reports and spreadsheets. This candidate will prepare, review, and submit reports in a timely manner. The candidate will utilize MAS200, Outlook, SQL, Excel, and Excel Power Tools daily. The candidate must be organized, detailoriented and self-motivated. The candidate must possess good oral and written communication skills. The candidate is required to preserve the confidentiality of any information that flows into the department and into the company as well as all information protected by HIPAA. Duties and Responsibilities:  Develop, update, and maintain Financial statement spreadsheets, databases, and applications that require daily, weekly, and/or monthly updates.  Ensuring monthly, quarterly, and annual reporting deadlines are met for financial audits, census and other reporting needs.  Reviewing internal financial activity and reporting for accur

Title: Regulatory Operations Specialist Reports to: VP of Quality & Regulatory Affairs Location: Remote initially then transitions to on-site (Irvine, CA office) Salary Range: $38-41.00 per hour (Non-Exempt, $79,000 - $85,000 annualized) Local candidates only; no relocation will be provided for this position. The Kardion Regulatory Affairs team is seeking a high energy, driven individual who is looking for the unique opportunity and challenge provided by a clinical stage startup. We are looking for a highly organized professional who excels at tracking and coordination of regulatory submissions, and wants to bring those skills to Kardion. The Regulatory Operations Specialist is a key partner within Regulatory Affairs to enable the team as a whole to create high quality submissions in a timely manner. This position requires someone with the ability to gather information from a variety of sources, keep track of a wide variety of deliverables and communicate status to the organization. Po

Kahana Feld is a nationally recognized, award-winning law firm with twelve offices across the country-and we're continuing to expand our team Summary The Paralegal will be responsible for working with attorneys and other departments and/or staff as assigned to provide support through all aspects of litigation in a variety of practice areas. Duties and Responsibilities: Under the supervision of an attorney, coordinate, organize, prepare, and interpret complex legal documents. Coordinate with attorneys and paralegal Is to direct workflow on various cases. Supervise paralegal Is on their duties performed and assist accordingly. Review and maintain documents and case files ensuring accuracy, organization, and confidentiality Compile pleadings for filing with courts and relevant agencies. Conduct electronic document reviews, coordinate productions of documents with attorneys, conduct searches of production databases for relevant documents, and conduct other related eDiscovery tasks. Assist

We are We are a global collective of innovators applying the New every day to improve the way the world works and lives. New doesnt mean being ahead of the curve; new is pushing forward the curve, riding the edge where the impossible meets the transformational and making it reality where it matters. Help us show the world whats possible as you partner with clients to unlock hidden value and deliver innovative solutions. Empowered with innovative tools, continuous learning and a global community of diverse talent and perspectives, we drive success in a new business architecture that disrupts conventional practices. Our expertise spans 40+ industries across 120+ countries and impacts millions of lives every day. We turn ideas into reality. You are As a member of one of the worlds largest Workday-certified teams, youll be part of a team of advisory professionals who deliver more than just technology. From rapid deployments to entire transformations, youll deliver integrated, payroll, clou

Job Description Job Description We are looking for an experienced and sharp CEQA / NEPA Technical Reports Specialist to join our team. This is a full-time position which can be based in any one of our CA offices (San Juan Capistrano, Diamond Bar, Long Beach, Ventura, Riverside, Los Angeles, San Diego, Temecula, San Francisco, Berkeley, or Santa Barbara). We offer competitive salaries, a full benefits package including Paid Time Off, Holidays, Full Medical/Dental/Vision, along with a 401k program with a generous company match. Position Summary: At Yorke, the CEQA / NEPA Technical Reports Specialist performs creative professional scientific work of considerable analytical difficulty as well as supervises and manages CEQA/NEPA services for the company, especially developing and producing technical studies and reports for various CEQA/NEPA documents. Responsibilities include directing and preparing all or portions of Initial Studies/Negative Declarations (IS/ND), Mitigated Negative Declara

Job Title: Product Compliance Specialist/Senior Specialist Reports to: Director II of Product Compliance Location: Los Angeles Job Status: Full Time About SHEIN SHEIN is a global fashion and lifestyle e-retailer committed to making the beauty of fashion accessible to all. We use on-demand manufacturing technology to connect suppliers to our agile supply chain, reducing inventory waste and enabling us to deliver a variety of affordable products to customers around the world. From our global offices, we reach customers in more than 150 countries. Founded in 2012, SHEIN has nearly 10,000 employees operating from offices around the world, with U.S. Headquarters located in Los Angeles and Global Headquarters located in Singapore. In SHEIN, we work with outstanding, creative, and capable peers. We share an energetic and open culture for capable people to discern, work and ignite as a team. Position Summary The Product Compliance Specialist/Senior Specialist will join our Americas Product Com