Denial Management Specialist Salary at Altair Health BETA

LabCorp is seeking a Specimen Management Specialist to join our team in Raritan, NJ. This position will work with internal customers, patients & physician offices to ensure that all patient care needs are addressed accurately and efficiently. The Specimen Management Specialist will provide product education and handle a wide variety of questions while providing market leading services. The ideal candidate will be passionate about improving health and improving lives. The schedule for this position will be: Monday to Friday 12 pm-8 :30pm with alternating Saturdays. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed

Job Title: Master Data Specialist Job ID: 25-06798 Location: Summit, NJ, 07901 Duration: 12+ months of Contract on W2 50% onsite Bachelor's degree required Work Schedule: Mon-Fri (normal business hours) Must Haves: Create, deploy, review, and sustain electronic systems Master Data. Perform data verification, system integration (LIMS, ERP, and MES) for electronic systems. Position Summary: Responsible for the creation and execution of computer system validation document as well as providing operational support and guidance related to system use and improvement. Duties/Responsibilities Create and execute computer system validation documents (i.e., UAT, URS, OQ, PQ, etc.) as applicable and guide QC end users on the development of system enhancements with user requirements and business drivers. Provide electronic systems operational support and troubleshooting to end user. Create, deploy, review, and sustain electronic systems Master Data. Perform data verification, system integration (LIM

Description LiveU is looking for a talented Order Management Specialist to join our team in New Jersey. We're looking for a motivated and diligent team player, that can give great service to our worldwide customers, and be the one that Liaise between Sales and internal departments. LiveU is a leader in live IP-video solutions for the world's top broadcasters, sports, public safety and other organizations. With over 5,000 customers in over 150 countries, LiveU is the brand name used to cover every major news and sports event, from the US Presidential Election campaign to the Summer and Winter Games. Main responsibilities include: •Manage international & multi-business model orders including correct and timely order entry in ERP. This will include the verification that such orders comply with company policies and are entered properly into the system to allow post sale processing (fulfilment, billing and post-sale support). •Support the sales cycle of muti business model orders - ORDER to

**39538BR** **Requisition ID:** 39538BR **Business Unit:** TSU **Job Description:** With high level goals provided, leads moderate to highly complex consulting analyses (e.g., operations improvement, Human Resources, organizational design, etc.) to support client business needs. With high level goals provided, leads the preparation of moderate to highly complex sections of management consulting reports. Leads the creation of basic to highly complex recommendations for improvements to client programs. With high level goals provided, contacts clients to collect or review datasets and/or presentations. Provides project status updates to clients, as required. Manages implementation plans as appropriate. Collaborates with sales staff to create proposals in response to current and potential client requests for proposal (RFPs). Reviews draft proposals for adherence to firm, industry, state, local and federal regulations and best practices. Meets with current and potential future clients to re

Consultant, Document Management Specialist II, Pharmaceuticals Summary Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a Document Management Specialist II to assist with U.S policy and SOP lifecycle document development and management. Description U.S. policy and SOP lifecycle document development and management. Includes tracking documents during the review/approval process, direct engagement with authors and teams, and following up with authors/teams to ensure deadlines are met. Managing documents in the Inkling content management system (CMS). Editorial updates and review (e.g., ensuring updates align with document guidelines and other policies and SOPs). Assist with digital content management, including building new and updating existing policies and SOPs, fixing broken links, and QC revised documents to ensure updates align 1:1 with author updates submitted via Word. Assist with document authoring for new and updated policies. Assist with m

GLG's Events team programs compelling insights driven meetings with global thought leaders and top practitioners, while managing all surrounding operational logistics. Position Overview GLG's Production Specialist leverages GLG's core asset - the GLG Network - to participate in small and midsize group meetings, roundtables, conferences, and seminars, both remote and in person, as well as virtual events including webcasts and teleconferences with clients and GLG Network Members. This position will focus on the development and programming of multiple meetings around select industry segments, which will vary by need, and will connect the industry's most notable experts with business and investment leaders throughout the world. Overall Values We seek bright, positive and flexible people who also: Act with the highest integrity and professionalism in all their endeavors Utilize superior analytical and problem-solving skills Think creatively and focus on opportunities for growth and lead oth

Document Management Specialist; Scientist Document Management Specialist will manage the documentation requirements of a large-scale re-formulation and manufacturability for a portfolio of consumer personal care products. Looking for candidates preferably with a Scientific background in formulation of Skin Health and Hair Care personal care products. The Document Management Specialist will be responsible for the following: Managing the documentation associated with Change Control process and other documentation for newly reformulated Skin Health and Hair Care products. Write Change Control and other technical documentation Manage Documentation including: Change Control, Specs, Supplier Notification, RMQ, Stability report, Safety Data Sheet (SDS), Obsolescence reports. Manage the timely delivery of pertinent docs being completed by other cross functional partners Working closely with cross functional partners who are providing documentation Strong technical writing skills Strong organiz

JOB SUMMARY: The IT Asset Management Specialist (ServiceNow) will be responsible for the administration and management of the organization's IT assets, ensuring effective lifecycle management from acquisition to disposal. This role requires strong expertise in using ServiceNow IT Asset Management (ITAM) to manage hardware, software, and license inventory, as well as ensuring compliance with asset related policies and standards. The specialist will work closely with IT, procurement, finance, and other departments to optimize asset utilization, reduce costs, and maintain accurate records. THIS IS A FULL-TIME, 3 MONTH, TEMP POSITION WITH A POSSIBILITY OF CONVERSION TO REGULAR EMPLOYEE STATUS. ESSENTIAL FUNCTIONS: • The functions listed describe the business purpose of this job or position. Specific duties or tasks may vary and be documented separately. An associate might or might not be required to perform all functions listed. Additional duties may be assigned, and functions may be modif