• Leads analysis on Population Health data sets and programs focusing on program financial performance • Works with external actuarial consulting team, internal finance, IT/analytics • Supports forecasting and scenario modeling • Ensures accuracy and integrity of financial datasets • Evaluates and translates performance in full risk arrangements • Analyzes claims, eligibility, and contractual data to identify financial trends, risks, and opportunities • Develops trend analysis reports that monitor key performance indicators • Provides ad hoc analyses to support financial planning and strategic initiatives

Computer System Validation Lead / Program Manager Ohio - Columbus Quality & Security & Compliance – Quality & Security & Compliance - NA / Full-Time / Remote Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors. As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment. Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities. The Role Join Veeva as we bring the power of modern, cloud-based digital validation to the industry. As a Computer Systems Validation Lead / Program Manager, you’ll lead the Validation supporting Veeva products (e.g., eTMF, CTMS, QMS, LIMS, etc.) – helping life sciences companies speed their adoption of a unified, cloud-based platform leveraging Veeva Validation documentation. We are seeking an experienced CSV professional to plan and support ongoing validation activities that includes general releases and patches/hot fixes for Veeva’s Quality applications. Drives the computer validation/qualification activities including developing/executing CSV deliverables (Business/Functional Requirements, Risk Assessments, Validation Plans/ Protocols, IQ, OQ, Validation Summary). Provides technical validation expertise, interpretation, and direction to assure compliance with industry and regulatory requirements (e.g., 21CFR211, Part 820, Part 11, Annex 11, ICH Q10, etc.), company policies and standards regarding validation, document control and change management. In this role, you’ll act as a trusted CSV planner, advisor, and partner with other Veeva teams. Through this partnership, you and your Veeva teams will deliver consistent and high-quality deliverables supporting Veeva life-sciences customers. This is a work anywhere, full-time permanent role with Veeva. Our work processes are designed so that you can be productive in the environment that works best for you. What You’ll Do - Lead and execute (as needed) the validation activities for Veeva’s general releases, hot fixes, as well as product periodic revalidation. - Responsible for tracking, monitoring, and controlling validation process to ensure timely delivery to meet pre-scheduled release dates and budgets. - Provide technical expertise, regulatory interpretation, and direction regarding computer validation, federal regulations, and other quality system requirements. - Closely collaborate with Product Team to ensure requirements/specifications are defined in a clear, testable, and compliant format. - Effectively work with cross functional teams (Product Management, SQA, Technical Operations, IT Engineering, etc.) to ensure the validated state of the system is maintained. - Ensure requirements are adequately tested following a risk-based approach. - Identify and log issues found during validation execution. Work closely with Product and SQA teams to identify and prioritize issues early on and track validation incidents to closure. - Ensure clear traceability against all testing performed. - Create/update CSV deliverables including IQ/OQ, VPP, VSR, Trace Matrices. - Independent pre and post execution review of validation test scripts - Coordinate with cross-functional teams to design and execute test protocols. - Supports change control as validation technical resource and ensures timely completion of required tasks. - Perform validation impact analysis and risk assessments in conjunction with product teams. - Execute other projects/duties as assigned to ensure compliance across Veeva’s product line and internal business systems. Requirements - Bachelor’s degree in Engineering/ Sciences or equivalent relevant technical experience - At least 3+ years of experience in CSV role - Hands-on experience with the validation of enterprise applications (e.g., SAP) used in the conduct of commercial regulated activities (Good Distribution Practice) and / or supporting industry applications (e.g., eTFM, CTMS, LIMS, Quality Management, DCS, etc.). - Good understanding of the relevant industry regulations (e.g., 21CFR11 / Annex 11, 21CRF211, 21CFR312, 21CFR203, 21CFR820, etc.) as well as industry standards /principles (ISO 9001, ASTM E2500, ISPE Baseline Guides). - Familiarity with Agile software development, business analysis and/or software testing methodologies. - Excellent written and oral communication skill, good decision-making skills and time management skills. Nice to Have - Experience with cloud-based applications, mobile applications and/or infrastructure compliance - Understanding of Agile development methodology - Understanding of CSA, RBV, use and Validation of AI in the life-sciences - Working knowledge of GAMP 5 Perks & Benefits - Medical, dental, vision, and basic life insurance - Flexible PTO and company paid holidays - Retirement programs - 1% charitable giving program Compensation - Base pay: $85,000 - $120,000 - The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus. #LI-Remote #LI-MidSenior Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Role Description Garud Technology Services is seeking an experienced Program Manager to lead delivery of IT Capital Planning and Investment Control, IT Financial Management, and Program/Project Management support for the USDA Farm Production and Conservation Business Operations Branch. This role serves as the contractor's senior leader for the engagement and is responsible for performance, staffing oversight, stakeholder coordination, and successful delivery of required contract artifacts and services. What you will do - Serve as the primary interface with the COR, Contracting Officer, federal leadership, and other government stakeholders. - Coordinate delivery across Task 1 Portfolio Management and Task 2 Financial Management workstreams. - Oversee required contract deliverables, including the Program Management Plan, Monthly Work Plans, Status Reports, and Transition Plans. - Manage scope, schedule, staffing, quality, risks, and issues across the program. - Ensure adherence to CPIC, FITARA, TBM, and federal IT lifecycle guidance. - Supervise contractor personnel and maintain compliance with quality, security, and schedule requirements. - Support monthly performance reporting, work planning, and accomplishment tracking required under the contract. Qualifications - Bachelor's degree, or qualifying substitute experience as defined in the JD. - 7+ years managing federal IT portfolio, capital planning, or financial management support programs. - PMP or PgMP preferred. - Experience working in federal shared-cost IT environments. - Strong leadership, client management, risk management, and technical writing skills. - Proficiency with Microsoft Office, SharePoint, and related collaboration tools. Additional requirements - Ability to obtain a favorable suitability determination and complete HSPD-12 credentialing before or at start, as required by the contract. - U.S. citizenship or lawful permanent resident status may be required for contract access. - Mandatory USDA training, including Information Security Awareness Training, is required for contractor personnel. Company Description Garud Technology Services, Inc. is a trusted provider of premier technology and engineering solutions for the U.S. government and private sector. Since 2004, Garud has delivered tangible results and measurable outcomes for clients with diverse and challenging missions. We are recognized for our commitment to exceptional service, our deep relationships across government, and our strong culture of compliance and accountability. Garud’s teams are highly skilled, nimble, and flexible, with the ability to rapidly develop and deploy new capabilities to achieve our customers’ goals.

The Role The Coordinator will be responsible for executing logistics for pharmaceutical educational events and ensuring that commitments are met on schedule and within budget. This person must maintain consistent communication with various internal and external stakeholders in a high-volume, deadline-driven environment. This is a hybird role with required in office time Tuesday, Wednesday and Thursday of each week. What You’ll Do - Database management - manage promotional educational programs within the proprietary system - Budget management - assisting customer representatives with their program planning budget to ensure they meet customer business rules and guidelines - Selection or confirmation of venue, menu, audiovisual, and air/ground transportation arrangements - Coordinate payment with venues/caterers and any other vendors - Frequent daily communication with sales representatives and faculty as needed - Review all venue contracts for accuracy/ensure customer compliance requirements are met - Ensuring all event materials are complete and accurate - Work closely with other team members to ensure successful execution of events - Adherence to various policies (i.e., confidentiality, sensitive communication, intellectual property) - Effectively manage a high volume of events while also responding to emails and phone calls - Manage and monitor a high volume of emails daily. - Cover after-hours phone line 5pm-midnight on a rotated basis (weeks selected by coordinator) Requirements - High School diploma or equivalent; College Degree Preferred - 1+ years experience in field or related area (Sales, Hospitality, Pharmaceutical, Medical Industry, and Customer Service) - Pharmaceutical Speaker Bureau experience is a plus - Pharmaceutical Event Planning experience is a plus - Strong analytical and problem-solving skills - Professional and clear oral and written communication and etiquette skills to successfully manage high phone and email volume - Demonstrate ability to work in a fast-paced environment, changing planning activities and/or multitasking often to meet fluctuating customer /company priorities - Proficiency in MS Office, Word, Excel (e.g., financial calculations, pivot tables, VLOOKUP’s), and Gmail preferred Nice to Have - Exceptional attention to detail - Ability to work and thrive in a team atmosphere - Positive attitude and maintain a “Whatever it Takes” attitude - Ability to take on additional ad hoc tasks as needed to support the team - Ability to maintain productivity while performing repetitive planning tasks every day Perks & Benefits - Medical, dental, vision, and basic life insurance - Flexible PTO and company paid holidays - Retirement programs - 1% charitable giving program Compensation - Base pay: $22 - $28 per hour - The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus. #LI-Entry Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.