Role Description GovCIO is currently hiring for an Operations Research Analyst / Data Scientist to support database development, data configuration, data analytics, and reporting activities at Department of Homeland Security (DHS) Immigration and Customs Enforcement (ICE). This role will be responsible for working within an interconnected reporting and analytics team to pull, configure, and analyze data to create real-time metrics, tasking responses, and overall information to support the ICE mission. This will be a fully remote position. - Provide effective data management to enable complex analytics from a myriad of systems and software including Oracle, Databricks, AWS, and ServiceNow. - Ability to align data with data analytic tools such as Power BI, Tableau, and Qlik Dashboards. - Facilitate the needs, issues, and challenges faced by the clients; perform gap analysis and recommend solutions that can be enabled within the data systems. - Provide trade-off analyses on technical solutions to determine the best tools and methodologies to solve complex data requests. - Create project deliverables, including artifacts to ensure adherence to team compliance and quality standards. - Use source data to assess the effectiveness of projects and business processes. - Work with all team members to analyze changes in requirements and recommend the most expedient solutions in a timely manner. - Enable end-user visibility of data and metrics via dashboard creation and metric dissemination. - Leverage advanced analytic skills to translate complicated issues from multiple information sources into a clear picture for mission leadership. Qualifications - Bachelor’s Degree or commensurate experience. - 5+ years of work experience (2 years of experience may be removed for a master's degree). - 2+ years of experience in data exploration, data cleaning, visualization, and overall data analytics. - 2+ years of experience in data visualization tools such as Qlik or PowerBI. Requirements - Experience in distributed data and computing tools including Databricks. - Experience with data modeling, mapping data flows, and data design. - Excellent data analytic and communication skills. - Strong analytical, problem-solving, and organizational abilities. - Ability to work independently in an extremely fast-paced environment. - Be flexible to change direction on a moment’s notice while also tracking/executing tasks in progress. - Ability to think “outside of the box” while communicating or dealing with a variety of situations. Clearance Required - Ability to attain and maintain DHS clearance (US citizenship required). Posted Salary Range USD $90,000.00 - USD $100,000.00 /Yr.

• Join our dynamic team at Biomapas as a Clinical Research Associate (CRA) in Ukraine. • Your role will be crucial in overseeing clinical trials and ensuring that they are conducted in compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. • Study site monitoring and management (site selection, initiation, monitoring and close-out visits) • Perform feasibilities and support start-up phase • Create and maintain required study documentation (site management, monitoring, etc.) • Ensure that clinical trials are conducted according to requirements (protocol, ICH-GCP, etc.) • Administer protocol and related study training to assigned sites • Perform regulatory document review • Prepare clinical trial documents and store, archive correspondence • Negotiate study budgets with potential investigators/sites, assist in agreements

Role Description The Sr. CRA will perform quality and compliant Investigator site monitoring and relationship-driven Investigator site management in line with MapLight’s SOPs, our Mission, Vision, and Values, as well as industry quality and regulatory best practices (ICH GCP). The CRA will perform on-site monitoring and centralized monitoring to ensure subject safety, the highest data integrity, and contribute to proactive risk management and inspection readiness. This role will collaborate closely with key cross-functional internal stakeholders including: - Clinical Operations - Medical Monitoring - Data Management - Supply Chain - Clinical Compliance and Quality External CRO and vendor partners will also be involved to ensure quality study oversight from study start up through close out. CNS and/or neuropsychiatry, specifically in-patient schizophrenia and/or Alzheimer’s disease psychosis or Alzheimer's disease agitation experience strongly preferred. Responsibilities - Effectively manage assigned Investigator sites and maintain positive relationships with site personnel. - Prepare for and conduct Pre-Study, Initiation, Interim and Closeout monitoring visits in accordance with MapLight SOPs and procedures, regulatory requirements and industry guidelines and best practices (ICH GCP). - Support the study team in meeting study milestones (site activation, DSMB meetings, database lock, etc.). - Perform centralized monitoring activities between on-site visits to ensure timely resolution of action items, oversight of study data quality and flow, and proactively identify and mitigate/manage study risks and issues. - Maintain quality and compliant documentation related to all aspects of site management including quality and ALCOA+ compliant monitoring visit reports, centralized monitoring reports, site contact reports, Trial Master File/Investigator Site File, etc. - Serve as the main MapLight point of contact for Investigator sites to support protocol compliance, streamlined communications, timely responses to site staff needs, and training needs. - Support the study team and Investigator sites during inspections or audits, as needed. - Perform other assigned tasks, as requested. - Support the study team(s) in development of study documents and procedures. - Support the development and maintenance of the study monitoring plan, templates, and tools. - Support the set-up, testing, and maintenance of study systems (EDC, eCOA, IRT, etc.) as well as related supporting documents (manuals, eCRF Completion Guidelines, etc.) in collaboration with MapLight and CRO/vendor study team members. - Continually review and reconcile the Trial Master File and Investigator Site File for assigned sites to ensure inspection readiness. - Maintain current knowledge of regulatory requirements and industry best practices related to monitoring, including centralized monitoring and risk-based monitoring. - Support development and process improvement for the MapLight monitoring function. - Support development and revision of SOPs, processes, templates, tools, and plans with the aim of continual improvement and streamlining. - Contribute to the maintenance and improvement of clinical systems to drive process improvement and efficiency. - Embody and demonstrate MapLight’s core values of Integrity, Collaboration, Bravery, and Dedication. Qualifications - Approximately 5 plus years in the clinical trial industry with at least 4 years of clinical monitoring experience including complex therapeutic areas, in-patient trials, and blinded trials. - CNS and/or neuropsychiatry, specifically in-patient schizophrenia and/or Alzheimer’s disease psychosis or Alzheimer's disease agitation experience strongly preferred. - Experience working in small/emerging biotech is ideal. - Experience managing multiple Investigator sites and multiple studies simultaneously. - Willingness to travel nationally to assigned Investigator sites as needed for required visits. - Ability to build relationships between Investigator sites and MapLight to foster strong collaboration, trust, and positive working relationships. - Strong working knowledge of Good Clinical Practices (GCPs), ALCOA+, and pertinent regulations. - Ability to engage collaboratively with internal and external stakeholders in a professional manner. - Strong interpersonal, oral, and written communication skills. - A self-starter with the ability to work independently and proactively. - Willingness to be a “team player” and take on additional responsibilities as requested. - Demonstrates core understanding of medical terminology and clinical trial activities in relation to execution of a clinical development plan. - High attention to detail and focus on quality and compliance in all aspects of assigned work. - Experience working in various clinical software systems (EDC, CTMS, eTMF, eCOA, EMR). - Proficiency with Microsoft Office applications (Word, Excel, PowerPoint, Outlook). - Ability to travel independently by air, car and/or train. Location near a major airport preferred. Benefits - Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. - Additional compensation/benefits include: - Annual bonus opportunity - Medical, dental, vision, life and AD&D - Short term and long term disability - 401(K) plan with match - Stock options - Flexible non-accrual paid time off - Parental leave Salary Range $145,000 — $160,000 USD EEOC Statement MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Role Description Join AIR as a Research Associate focused on Medicaid Policy and Programs with our Healthcare Innovations team. Our team works collaboratively to address complex challenges related to Medicaid coverage, care delivery, cost containment, and health equity, supporting federal and state partners in improving outcomes for low‑income and medically vulnerable populations. The Research Associate will report to AIR's Healthcare Innovations Team, which supports high-quality implementation and produces rigorous evidence on the effectiveness of new approaches to care and payment—translating findings into actionable insights for policymakers, payers, providers, and patients. This role will contribute directly to studies that inform Medicaid policy design, program evaluation, and system transformation. This position has the flexibility to work remotely within the United States (U.S.) or from one of AIR’s U.S. office locations. This does not include U.S. territories. Responsibilities - Assist project teams in compiling and synthesizing information (e.g., conducting literature reviews and policy scans). - Prepare and assist with primary source data collection through interviews, focus groups, and surveys; organize materials; and contribute to content development. - Participate in the collection and review of research and evaluation data. - Analyze quantitative and qualitative research data and contribute to the reporting and interpretation of findings. - Prepare documents, portions of reports, briefs, charts, and graphs that describe and interpret findings of analyses. - Support proposal writing and business development activities. - Support project management tasks, including developing project timelines, coordinating meetings, and tracking project progress. Qualifications - Bachelor’s degree with 2+ years of experience, or a Master’s degree in the social sciences or related fields. - Direct experience with Medicaid policy and/or data is required. - Experience conducting quantitative and/or qualitative data collection. - Experience using or working on analyses with Python or R, highly desirable. Skills - Attention to detail and commitment to accuracy in data collection and report writing. - Ability to work independently and as part of a team. - Proficiency with the Microsoft Office Suite. - Effective communication skills with the ability to collaborate efficiently in a virtual work environment. - Excellent organizational and time management skills. Disclosures - Applicants must be currently authorized to work in the U.S. on a full-time basis. Employment-based visa sponsorship (including H-1B sponsorship) is not available for this position. - Depending on project work, qualified candidates may need to meet certain residency requirements. Accessibility Notice If you need a reasonable accommodation for any part of the employment process due to a physical or mental disability, please send an email to Taliba Boone at tboone@air.org or call 202.403.5000. Fraudulent Job Scams Warning & Disclaimer AIR is aware of individuals falsely presenting themselves as AIR representatives. Fraudulent job scams seek to extract sensitive information or money from victims. To protect yourself, please be aware that AIR recruitment will only email you from an “@air.org” domain. Please take extra caution while examining the email address, for example jdoe@air.org is correct and jdoe@aircareers.org is not a legitimate AIR email address. If you are unsure of the legitimacy of a communication you have received, please reach out to recruitment@air.org . If you see a job scam, or lose money to one, report it to the Federal Trade Commission (FTC) at ReportFraud.ftc.gov . You can also report it to your state attorney general. Find out more about how to avoid scams at ftc.gov/scams . Benefits - Anticipated Hourly Rate Range: $33 — $40 USD