• Lead the development, implementation, and optimization of EpicCare Ambulatory • Design, build, test, and maintain Epic system components to streamline clinical workflows • Partner with clinicians and stakeholders to analyze business needs and create innovative solutions • Configure workflows, documentation tools, Smart Tools, OTX, Health Maintenance, Registries, and more • Provide technical expertise, training, and ongoing support for end users • Collaborate on projects, system enhancements, and process improvements to enhance operational efficiency and patient safety

Role Description The Medical Economics Senior Analyst oversees the design, development, and delivery of regulatory reports and financial analyses that support Mass General Brigham Health Plan’s external filings and internal interpretation of results. This role requires expertise in financial regulatory reporting. Hands-on experience with Center for Health Information and Analysis (CHIA), Division of Insurance (DOI), and Center for Medicare and Medicaid Services (CMS) submissions is strongly preferred. - Translate complex regulatory specifications into actionable data logic. - Ensure accurate and timely report production. - Identify key drivers of cost, utilization, and performance. - Guide and develop junior staff in reporting workflows. - Partner closely with Actuarial, Finance, Provider Network Management (PNM), Pharmacy, and Product teams. - Support a broad regulatory portfolio, including CHIA submissions and DOI utilization reporting. - Serve as the subject matter expert for regulatory reporting. Qualifications - Bachelor's Degree required; experience can be considered in lieu of a degree. - At least 5-7 years of experience in data analysis required. - Experience running CHIA Pharmacy Rebate, RxDC, Premium, Relative Price, Total Medical Expenses and Alternative Payment Methods (TME-APM), Primary Care and Behavioral Health (PC-BH), and DOI utilization reports is highly preferred. - Strong knowledge of relational databases, SQL, data visualization, and Business Intelligence tools, such as Tableau. - Strong proficiency with Microsoft Office Suite, including Word, Excel, and PowerPoint. - Ability to communicate complex workflows and data to a variety of audiences. - Project management skills and/or experience are a plus. - Knowledge and application of statistical analyses, including variance analysis and statistical significance preferred. - Healthcare knowledge, particularly as it pertains to electronic medical record data, is preferred but not required. Requirements - Remote role that can be done from most US states. - Schedule is Monday through Friday, 8:30 AM - 5:00 PM Eastern. - Employees must use a stable, secure, and compliant workstation in a quiet environment. - Teams video is required and must be accessed using MGB-provided equipment. Benefits - Competitive salaries. - Flexible work options. - Career growth opportunities. - Comprehensive benefits package.

Role Description We are seeking a detail-oriented and technically capable IAM Analyst II to join our Corporate Identity and Access team, embedded within one of our high-growth technology clients. This role owns application integration work, handles escalated access tickets, and serves as a point of coordination between application owners, vendors, and the broader identity team on complex integrations. This position starts as part-time with a clear path to full-time as the engagement grows. It sits at the intersection of IT operations and identity engineering — a great fit for someone who thrives in both execution-focused and relationship-facing work. Key Responsibilities - Execute and manage SaaS application integrations, including direct coordination with application owners and external vendors on complex configurations. - Triage and resolve escalated access tickets from the IT Operations team, driving issues to resolution or escalating appropriately. - Support user lifecycle workflows, including provisioning and deprovisioning across a broad SaaS portfolio. - Maintain and improve documentation, runbooks, and process guides for integration and access workflows. - Assist with audit evidence collection and access review activities to support compliance requirements. - Partner with Security, IT, and People Operations teams to ensure access is governed consistently and at scale. Qualifications - 2+ years of experience in IT operations, identity and access management, or a closely related field. - Hands-on experience with Okta or a comparable IAM platform (Azure AD / Entra ID). - Experience with SaaS application integrations, including SCIM provisioning and SSO configurations. - Comfortable engaging directly with application owners and external vendors to troubleshoot and complete integrations. - Familiarity with IT service management and ticketing systems (Jira, ServiceNow, or similar). - Strong attention to detail with the ability to follow and continuously improve established processes. - Ability to work independently in a remote capacity with minimal supervision. Requirements - Basic scripting or automation experience (Python, JavaScript, or similar). - Exposure to identity governance and access review processes. - Experience supporting audit evidence collection in a SOC 2 or similar compliance environment. Salary Range $20.23 - $25.29 USD (Hourly) Please note that the salary information provided herein is base pay only (gross); it does not include other forms of compensation which may or may not apply to this specific position, namely, performance-based bonuses, benefits-related payments, or other general incentives - none of which are guaranteed, may be subject to specific eligibility requirements, and are wholly within the discretion of Astreya to remit. Further, the salary information noted above is a range that consists of a minimum and maximum rate of pay for this specific position. Where an applicant or employee is placed on this range will depend and be contingent on objective, documented work-related considerations like education, experience, certifications, licenses, preferred qualifications, among other factors. Benefits - Medical provided through UHC (PPO, HSA, Surest options). - Medical provided through Kaiser (HMO option only) for California employees only. - Dental provided through UHC. - Nationwide Vision provided by UHC. - Flexible Spending Account for Health & Dependent Care. - Pre-Tax Account for Commuter Benefit/Parking & Transit (location-specific). - Continuing Education and Professional Development via various integrated platforms, e.g. Udemy and Coursera. - Corporate Wellness Program provided by Goomi Group. - Employee Assistance Program. - Wellness Days. - 401k Plan. - Basic and Supplemental Life Insurance. - Short Term & Long Term Disability. - Critical Illness, Critical Hospital, and Voluntary Accident Insurance. - Tuition Reimbursement (available 6 months after start date, capped). - Paid Time Off (accrued and prorated, maximum of 120 hours annually). - Paid Holidays. - Any other statutory leaves, paid time, or other ancillary benefits required under state and federal law.

Role Description The Investigator Contracts Lead (ICL) is responsible for direct site facing contract and budget negotiations through contract execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the Per-Subject Cost (PSC) process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other ICL or preferred Contract Research Organizations (pCRO) and collaborating with other lines to plan site contracting timelines though start up. Key Accountabilities - Exercise good judgment in balancing the risks to the sponsor in making budget and contractual decisions against the impacts to client clinical trial timelines. - Follow processes to develop, negotiate, track, and execute global clinical study agreements with institutions and investigators participating in sponsored clinical trials. - Work with partners to develop and oversee the global site budget process. - Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions with investigators/institutions, making changes to contract templates within the Legal division approved parameters. - Lead study level site contracting activities and act as primary study point of contact for site contracting issues and timelines on assigned studies. - Partner with Legal and other divisions to manage escalations in the site budgeting and contracting space. - Partner with Legal, Finance, pCRO and other divisions to identify and implement areas of improvement in the site contracting space. Collaboration - Lead and develop relationships with key investigational sites and Site Management Organizations across the contracting and budgeting interface. - Collaborates with invoicing specialists and/or invoice service provider to ensure alignment with Investigative Site contracting and compensation requirements. - Interacts with clinical site contracts & legal contacts, client and partner legal team, study management, site payments team, peer site contracting colleagues, and CRO site contracting teams. - Contributes to design, development and implementation of major business initiatives or special projects where required. Qualifications - Balance of general business, compliance, finance, legal, and drug development experience. - Precise communications and presentation skills. - Ability to plan, identify and mitigate risks to site contacting timelines. - Ability to lead by influence rather than positional power to accomplish critical deliverables. - Success in working in a highly matrix-based organization. - Fluency in written and spoken English is required. - Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities. - Experience in drafting and negotiation of Clinical Trial Agreements with clinical trial sites in a global operation is preferred. Education - Bachelor’s Degree or equivalent and 5+ years of experience in clinical development operations or clinical trial outsourcing OR PhD/Doctorate or equivalent and 2+ years of experience in clinical development operations or clinical trial outsourcing. Not quite the role for you? Join Our Talent Community and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events. Sign up today: https://jobs.parexel.com/functional-service-provider