• Develop, administer, and implement environmental programs in accordance with applicable federal, state, and local governmental requirements • Monitor pollution prevention activities, environmental compliance programs, and auditing efforts to ensure adherence to environmental regulations and company policies • Conduct environmental studies and prepare environmental impact reports associated with new construction projects, facility modifications, operational processes, and permit changes • Review and analyze environmental documentation issued by regulatory agencies and determine impacts to organizational operations and mission execution • Develop and publish compliance strategies, guidance, and implementation requirements to ensure organizational readiness and regulatory alignment • Evaluate proposed environmental regulations and policies to assess financial, industrial, operational, public, and environmental impacts • Coordinate and interact directly with regulatory agencies and stakeholders to resolve environmental compliance issues and support permitting activities • Represent HII and supported organizations during government, industry, and regulatory rule-making activities, meetings, and working groups • Support energy resilience, sustainability, infrastructure modernization, and environmental stewardship initiatives aligned with Department of Defense priorities • Provide leadership, mentorship, and technical guidance to engineering and environmental support personnel as required • Prepare technical reports, briefings, risk assessments, and executive-level presentations supporting program leadership and customer engagements

Role Description As a Lead Clinical Research Associate, you will hold a leadership role within the study team, overseeing and guiding the clinical team while driving trial activities at a country or regional level. You will ensure high-quality execution, compliance, and timely delivery. You will act as a key point of coordination across cross-functional teams. This role focuses on leadership, mentorship, oversight, and consistency in monitoring practices rather than direct site management, with minimal to no site assignments and a low-travel model, emphasizing remote oversight and overall study quality. Responsibilities: - Monitors project timelines, patient enrollment, data cleaning, and ensuring compliance while implementing respective corrective and preventive measures. - Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Monitors in the region. - Acts as the main communication line between Monitor, Site Management Associate, Regional Project Lead, and/ Project Manager. - Leads project team calls on a country level as well as provides status updates and reports to Regional Lead/ Project Manager. - Provides project-specific training and prepares training materials for the project team under supervision of a Project Manager and Regional Project Lead. - Supervises source data verification and follows up on data queries at site level in the country/region; reviews and manages study risks on a site level. - Ensures proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on a country/region level. - Reviews essential study documents and supervises reconciliation of study Investigator Site File (ISF) / TMF at site level and country/region level. - Ensures data integrity and compliance at a site level. - Collaborates with investigator/site feasibility and identification process, as well as study startup. - Manages Monitors in the query resolution process, including Central Monitoring observations. - Coordinates safety information flow and protocol/process deviation reporting. - Performs clinical supplies management with vendors on a country and regional level. - Ensures study-specific and corporate tracking systems are updated in a timely manner. - Coordinates planning of supervised monitoring visits and conducts the visits. - Manages the project team in site contracting and payments. - Ensures ongoing evaluation of data integrity and compliance at a country/regional level. - Conducts site audit preparation visits, may participate in site audits, and coordinates resolution of site audit findings on a country/regional level. - Oversees project team in CAPA development and implementation. - Coordinates project team in process deviations review, management and reporting. - Conducts initial training and authorization monitoring visits for Monitors and acts as a mentor for newly promoted Lead CRAs. - Delivers trainings and presentations at Investigator Meetings. - Ensures that subject recruitment targets and project timelines are properly defined, communicated, recorded, and met at site level. - Ensures accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations. - Supervises Site Management Associates in the flow of documents and laboratory supplies between the site and the Central/Regional Lab/Central Reviewer. - Supports preparation of draft regulatory and ethics committee submission packages. Qualifications - Relevant educational background, such as MD, MPharm, RN or College/University degree in Life Sciences or an equivalent combination of education, training and experience. - Minimum of 4 years’ site monitoring experience with participation in global clinical projects as a Lead Monitor or equivalent qualification level. - Experience with all types of monitoring visits in Phase II and/or III. - Strong experience in Oncology preferred. - Experience in Radiation Therapy or Radiopharmaceuticals, CAR-T Therapy or other types of Cell Therapy, Gene Therapy, or Nuclear Medicine is preferred. - Strong experience in GI (Chron's, Ulcerative Colitis, IBS) preferred. - Full working proficiency in English. - Proficiency in MS Office applications. - Ability to plan, multitask and work in a dynamic team environment. - Excellent Communication, collaboration, and problem-solving skills. - Ability to travel. - Valid driver’s license (if applicable). Additional Information If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.

Role Description The Senior Lead Finance Analyst will play a critical role in managing and optimizing Operating Expenses (OPEX) across the enterprise. This position combines strong financial acumen with advanced technical skills, including AI-driven analytics, to deliver actionable insights and support strategic decision-making. The ideal candidate will partner with cross-functional teams to ensure accurate forecasting, budgeting, and reporting while driving automation and efficiency. Work Location: This position has been designated as fully remote in the U.S. Main Responsibilities - OPEX Planning & Forecasting - Build and maintain dynamic OPEX models leveraging advanced analytics and scenario planning. - Apply predictive modeling techniques (e.g., regression, time-series forecasting) to improve forecast accuracy. - Utilize AI-driven tools for anomaly detection and trend analysis in expense patterns. - Financial Analysis & Insights - Perform deep-dive variance analysis, identifying root causes and actionable recommendations. - Develop dashboards using Power BI or similar visualization tools to present real-time OPEX performance. - Integrate machine learning algorithms to identify cost optimization opportunities and automate repetitive analysis tasks. - Business Partnering & Strategic Support - Act as a trusted advisor to operational leaders, translating complex financial data into strategic insights. - Collaborate with cross-functional teams to align OPEX strategies with enterprise objectives. - Use natural language processing (NLP) tools to summarize large datasets and meeting transcripts for decision-making. - Process Automation & AI Enablement - Drive automation of reporting processes using Python, R, or SQL scripts integrated with financial systems. - Implement AI-based solutions for expense categorization and predictive spend management. - Partner with IT and data science teams to deploy machine learning models into financial workflows. - Data Governance & Compliance - Ensure data integrity and compliance with corporate financial policies and regulatory standards. - Apply AI-powered audit tools to detect anomalies and strengthen internal controls. - Maintain robust documentation for models, assumptions, and methodologies to support transparency. Qualifications - Bachelor’s degree in Finance, Accounting, or related field; MBA or CPA preferred. - 5+ years of experience in financial planning and analysis, with a focus on OPEX. - Strong analytical, problem-solving, and communication skills. - Ability to manage multiple priorities in a fast-paced environment. Requirements - Technical Skills & Proficiencies - AI/ML Tools: TensorFlow, PyTorch, Scikit-learn for predictive analytics. - Data Visualization: Power BI, Tableau, or similar platforms. - Programming: Advanced skills in Python and SQL for automation and data manipulation. - Cloud & Data Platforms: Familiarity with Azure Data Services or similar enterprise cloud environments. - Financial Systems: SAP, Oracle, or equivalent ERP systems. - Data Science Concepts: Predictive modeling, anomaly detection, and NLP for financial applications. Compensation This information reflects the anticipated base salary range for this position based on current national data. Minimums and maximums may vary based on location. Individual pay is based on skills, experience, and other relevant factors. - Location Based Pay Ranges: - $105,786 - $141,047 in these states: AL, AR, AZ, FL, GA, IA, ID, IN, KS, KY, LA, ME, MO, MS, MT, ND, NE, NM, OH, OK, PA, SC, SD, TN, UT, VT, WI, WV, WY - $111,074 - $148,099 in these states: CO, HI, MI, MN, NC, NH, NV, OR, RI - $116,364 - $155,152 in these states: AK, CA, CT, DC, DE, IL, MA, MD, NJ, NY, TX, VA, WA Benefits - Lumen offers a comprehensive package featuring a broad range of Health, Life, Voluntary Lifestyle benefits and other perks that enhance your physical, mental, emotional, and financial wellbeing.

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects • Conduct study initiation visits (SIVs)