Location: REMOTE in OH State Work Schedule: Schedule is Monday – Friday, 8am-5pm, standard business hours. No required holidays or weekends This role serves as the "Front desk" to the plan. This individual will work on a variety of administrative tasks to assist the Care Coordination department that may include but are not limited to, the inbound care management queue line, responding to questions and inquiries from both members/guardians or parties assisting with services. They will be responsible for taking referrals, confirming their Medicaid eligibility and processing the referral. This role will also complete Health Risk Assessments for all members assigned. It is imperative that the CMA must be able to practice both a high level of professionalism and compassion at all times when interacting with various departments or member representatives. The CMA will also support administrative needs that involve comfortability with working in complex data systems, an Electronic Record System and/or Excel at any given time. Tasks can change with little notice to meet the demands of the health plan requiring flexibility.

Through the use of care management tools and information/data review, conducts comprehensive evaluation of referred member's needs/eligibility and recommends an approach to case resolution and/or meeting needs by evaluating member's benefit plan and available internal and external programs/services. Identifies high risk factors and service needs that may impact member outcomes and care planning components with appropriate referral to clinical case management or crisis intervention as appropriate.

Must be well organized and able to accurately prepare, catalog and electronically store information. Strong communication skills, QA/QC experience* This assignment is to provide operational project support to assess different information inputs (moderate to complex data) that will be used in various pricing initiatives. The role will aggregate the data based on defined requirements to a single output for consumption by other areas in the organization. Strict attention to detail is essential to the role – the results could be subject to future audits.

The Clinical Programming Manager is responsible for managing the timely and accurate execution of programming components of clinical trials. The Manager leads and manages completed projects that involve global tasks, cross functional teams, or outsourcing resources. The role may require providing input to design and analysis, and report the results of clinical trials, including programming rules and mocked T/L/G. In addition, providing all safety claims for new drugs and extension of claims/publication support for our marketed drugs.

As an Analyst I supporting Colleague Relations, you will serve as the primary point of contact for our colleagues, offering expert guidance on a broad range of issues and concerns, including but not limited to reasonable accommodation, workforce reduction, colleague performance, attendance and policy interpretation. In this role, you will respond to a significant volume of calls from colleagues seeking guidance. You will provide timely and effective solutions to colleague issues during the initial contact. Additionally, you will provide cross-functional support to other departments as required. Colleague Relations is a Health Human Resources Center of Excellence. We are ambassadors of our Company's culture. We strive to promote a positive, healthy working environment. We demonstrate respect, care, and empathy toward all colleagues while applying a fair, balanced approach to resolve policy related colleague concerns.

Location : Winamac, IN 46996 (Onsite). The Project Timekeeper will support payroll and timekeeping activities for craft professionals on the Winamac, IN project site. The role requires accuracy, confidentiality, strong organizational skills, and flexibility to work overtime, weekends, and occasional travel.

Location: Durham (RTP) NC 27709. • Manages a piece of the ongoing program activity of the Syncade migration project for LSM, mainly focused on the stakeholder collaboration. • This position will support the Large-Scale Manufacturing (LSM) Modernization project for bringing a new Manufacturing Execution System (MES) to the drug substance manufacturing area. This system will encompass several phases covering electronic equipment tracking, electronic batch records and release by exception functionalities. This role will be supporting the operational readiness workstream and activities associated with ensuring the site is ready to receive this change and sustain it within routine production operations. • Looking for candidates in line with a senior leadership, strategy, directive role and not at a mid-level, day-to-day hands-on working perspective. While having a good technical basis in MES system is helpful and desired the individual needs to have just as much experience in the operational, quality, side to assist with mapping business processes, building schedules, setting up performance tracking, and other elements of project management & leading the integration of these with the technical MES side.

Location (mandatory): Irving, TX Business Systems Analyst Senior- Min 3yrs experience; required healthcare provider experience (hospitals, clinics), not insurance. Candidates have a solid background in implementation, strong communication skills are a must, individual who can articulate their ideas clearly and effectively, both verbally and in writing.

Location - Cambridge, MA 02141 or Morristown, NJ 07960 (Onsite). Position Title: Senior Strategic Procurement Consultant. Role Purpose: Support External Manufacturing Procurement team with strategic negotiations, project management, sourcing optimization initiatives, and capability building. • This position will help Global Procurement deliver strategic work. • 10+ years of experience in strategic procurement/sourcing, preferably in pharmaceutical/biotech industry. • Consultants from Top tier consultation firms preferred • Onsite in either: Cambridge/MA or Morristown/NJ