This page tracks remote principal openings that are location-eligible for Iowa.
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58 Jobs
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• Cutover planning and execution of comprehensive step-by-step mock, rehearsal and production cutover management plan. • Drive cutover progress, including task completion, milestone achievement to adhere to overall timeline. • Lead Daily meetings with cross functional thread leads. • Understanding team member workload, task timing, potential resource constraints, and ensure optimal resource utilization throughout the cutover process. • Proactive risk management: identify, assess, mitigate, and monitor potential risks with real-time alerts for critical issues. • Monitor and track cutover metrics, including issues and task timing. • Communicate expectations and instill accountability in team members. • Resolve conflicts, promote work sharing, and motivate teams toward common goals. • Manage multiple cutover activities, tasks and resources through effective organization prioritization, and time management practices to meet program objectives. • Additional responsibilities include documentation and reporting, internal stakeholder communication, and identifying areas for improvement to enhance quality and efficiency of cutover activities. • Ability to travel ~ 25%-50% to other major RTX US sites (Farmington, Richardson, Cedar Rapids, and Charlotte).
• Contribute to statistical activities related to global clinical trials • Work closely with international teams of statisticians, programmers and data managers • Act as a communication line for project teams, clients, vendors and internal team on statistical questions • Conduct statistical analysis for clinical trials • Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents • Review statistical deliverables such as tables, figures, listings and analysis datasets • Conduct departmental induction course and project-specific training for statisticians and SAS programmers • Prepare for and attend internal and external study audits pertinent to Statistics • Participate in preparation of internal/external audits follow up • Provide input to standard operating procedures and other Quality Systems Documents pertinent to activities of Biostatistics department • Liaise with DM on statistical questions related to data issues • Participate in bid defense and in kick-off meetings • Lead teams of SAS programmers and/or statisticians on the project level
YA Group is an international professional services organization providing forensic consulting, engineering, risk mitigation, and related services. Founded over 25 years ago as a property damage consulting firm, YA has expanded through organic growth and strategic acquisitions. Today, YA has over 800 professionals dedicated to excellence, partnership, and driving innovation. YA Engineering Services (“YAES”) is a national forensic multi-disciplinary consulting firm. YAES provides immediate response to new assignments, performs investigations in a timely manner, and provides comprehensive reports that are clear, concise, and backed by reasonable analyses and recommendations.
Role Description The Senior Toxicologist will lead consulting projects involving chemical exposures, environmental contamination, and human health risk. They will provide independent, science-based analysis to attorneys, insurers, corporate clients, and public agencies, helping them understand complex technical issues and make informed decisions. This role will serve as a trusted expert in litigation, forensic investigations, regulatory matters, and risk management, delivering clear, defensible conclusions when the stakes are high. The Senior Toxicologist will also build strong client relationships, expand professional networks, and contribute to the growth of the practice. - Lead toxicology assessments addressing human health, exposure pathways, and risk in both litigation and regulatory contexts - Serve as a retained expert witness, preparing expert reports and providing deposition and trial testimony - Review and analyze legal documents, medical records, industrial hygiene data, laboratory results, and scientific literature - Evaluate toxicological studies and exposure data to develop clear, well-supported conclusions - Coordinate with laboratories and assess the quality and reliability of analytical data - Prepare technical reports that support litigation, regulatory matters, and client decision-making - Support forensic investigations and proactive risk assessment projects for clients - Build and maintain long-lasting relationships with attorneys, insurers, industry professionals, and regulatory agencies - Identify new business opportunities and grow a book of reoccurring client work in line with individual revenue goals - Perform additional duties as assigned Qualifications - Degree in Toxicology, Environmental Health, Environmental Sciences, Biological Sciences or equivalent years of experience - DABT certification required - 10+ years of professional toxicology practice, with substantial work supporting litigation matters - Strong understanding of litigation-related toxicology, including the analysis of case files, medical records, exposure data, and peer-reviewed research - Experience managing laboratory partners and evaluating analytical and industrial hygiene data - Demonstrated experience presenting expert opinions through written reports, depositions, and courtroom testimony - Strong technical writing and communication skills, with the ability to explain complex scientific information to a variety of audiences Benefits - Employee-focused culture - Strong commitment to work-life balance - Remote work - Flexible vacation & Paid holidays - Paid family care/sick leave - Parental leave - Medical, Dental, Vision + more - 401k w/match - Career growth - Competitive salaries + Bonus Company Description YA Group is an international professional services organization providing forensic consulting, engineering, risk mitigation, and related services. Founded over 25 years ago as a property damage consulting firm, YA has expanded through organic growth and strategic acquisitions. Today, YA has over 800 professionals dedicated to excellence, partnership, and driving innovation. YA Group's Environmental Services division delivers comprehensive environmental, health, safety, industrial hygiene, building sciences, and due diligence consulting to private and public sector clients. With nearly 20 years of experience and over 100 years of combined expertise, our team of certified professionals — including CIHs, LSRPs, CIECs, and CMCs — assesses a broad range of hazards such as mold, asbestos, lead, smoke, indoor air quality concerns, and subsurface soil and groundwater contamination, providing actionable remediation protocols and clarity-driven reports that ensure safety, regulatory compliance, and peace of mind across projects of all sizes.
• Lead the development of brand and campaign platforms — translating strategy into big, extensible ideas that scale across channels and contexts. • Activate the Engine brand across a wide range of initiatives including integrated campaigns, digital experiences, growth campaigns, product launches, and brand moments. • Own projects from brief through delivery — setting creative direction, driving decisions, and maintaining a high creative bar at every stage. • Partner closely with Brand Strategy to ensure creative work is grounded in sharp insight, clear positioning, and strategic intent. • Lead and inspire multi-disciplinary creative teams and agency partners, providing clear direction and meaningful feedback throughout the creative process. • Oversee smaller, highly creative projects with the same ambition and craft as large-scale campaigns, no project is too small to be exceptional. • Present creative concepts and campaign platforms to senior stakeholders and executive leadership with clarity and conviction. • Identify opportunities to extend and evolve the Engine brand into new channels, formats, and moments.
Role Description The Capital Markets Associate will work with the broader Treasury team to oversee ongoing reporting requirements and to assist in sourcing both short- and long-term funding for PACE assets originated by the company. Success in this role will be predicated on the ability to comprehensively understand nuanced capital markets concepts and clearly communicate these with external and internal stakeholders to reliably achieve satisfactory financing outcomes in support of various company initiatives. Core Responsibilities - Support the negotiation and closing of financing transactions (securitizations, forward flows, whole loan sales, and warehouse facilities), including: - Business term negotiation - Legal document review - General due diligence - Coordination with rating agencies and other service providers - Data-tape preparation - Creation of investor presentations - Support with Green Bond accreditation - Update and maintain recurring reports detailing new PACE asset originations and the distribution of cash flows through existing financing structures. - Process reports automated via Python, Google Colab, SQL, and Tableau in a timely manner; in the long term, identify incremental process efficiencies. - Maintain and update a centralized database for the Treasury team. - Respond to ad hoc data requests on asset performance (e.g., prepayments, property tax payments, audits), the company’s hedging program, corporate liquidity, and profitability optimization. Additional Responsibilities - Cross train on other Treasury team tasks for backup purposes. - Support liquidity management and maintain an interest-rate hedging program designed to mitigate the Company's sensitivity to market rate fluctuations. Qualifications - Bachelor’s Degree in business, economics, engineering or other field with significant quantitative coursework, or equivalent experience. - 2-5 years’ experience in Structured Finance, Project Finance, Renewable Energy Finance, or related fields. - Advanced knowledge and experience working with Microsoft Office (.xls, .ppt, .doc), with a focus on Excel. - Coursework and/or experience working with SQL and Python programming languages. Requirements - VBA experience in Excel. - MBA degree, or equivalent experience. Location Remote (U.S. – limited to specific states) While this role is remote, at this time we are only able to consider candidates who reside in the following states due to employment registration and tax requirements: - Arizona - California - Colorado - Delaware - Florida - Georgia - Idaho - Maryland - Massachusetts - New York - North Carolina - Oregon - Pennsylvania - Texas - Utah
Role Description The Senior Sterilization Microbiologist is responsible for leading the development, validation, and ongoing control of sterilization processes (e.g., EO, steam, radiation) to ensure product safety, regulatory compliance, and process robustness. This role provides technical expertise and strategic direction for microbiological aspects of sterilization across manufacturing and quality systems. This position is remote to enhance our competitive edge and expand our cross-functional collaboration efforts. This role will require 10% of travel to enhance collaboration and ensure successful completion of projects. Key Responsibilities - Lead sterilization validation activities (IQ/OQ/PQ, MPQ/PPQ) for new and existing products. - Develop and review sterilization protocols, reports, and cycle parameters. - Serve as SME for sterilization processes (EO, Gamma, E-beam, Steam). - Ensure compliance with regulatory standards (FDA, ISO 11135, ISO 11137, ISO 17665). - Support investigations related to bioburden, sterility failures, and deviations. - Oversee bioburden, endotoxin, and environmental monitoring programs. - Collaborate with cross-functional teams (Quality, Engineering, Operations, external suppliers like sterilization vendors). - Review and approve changes impacting sterilization processes. - Provide guidance during audits and regulatory inspections. - Drive continuous improvement initiatives in sterilization and microbiology processes. Qualifications - Requires a Bachelor's degree and minimum of 4 years of relevant experience OR Master's degree with a minimum of 2 years relevant experience OR PhD with 0 years relevant experience. - Requires a Bachelor’s or Master’s degree in Microbiology, Biology, or related field. - Requires 5 to 10 years of experience in sterilization microbiology (medical devices/pharma preferred). - Strong knowledge of sterilization validation and microbiological methods. - Experience with regulatory submissions and audits. - Experience with LIMS, SAP, MES, and BPCS required. - For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. Benefits - Competitive Salary and flexible Benefits Package. - Health, Dental and vision insurance. - Health Savings Account. - Healthcare Flexible Spending Account. - Life insurance. - Long-term disability leave. - Dependent daycare spending account. - Tuition assistance/reimbursement. - Incentive plans, 401(k) plan plus employer contribution and match. - Short-term disability. - Paid time off. - Paid holidays. - Employee Stock Purchase Plan. - Employee Assistance Program. - Non-qualified Retirement Plan Supplement (subject to IRS earning minimums). - Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
• Serve as a trusted advisor to C-suite executives • Lead the diagnosis and resolution of complex client problems • Define and articulate the strategic vision for client projects • Own the delivery of all projects ensuring client value • Identify, qualify, and lead new business opportunities • Oversee strategic client relationships and ensure portfolio growth • Author high-impact white papers and presentations
An engineering firm that delivers high-quality Healthcare IT, Cybersecurity, and Telecommunication solutions.
• Lead the scaled agile delivery model across the program, including PI Planning coordination, cross-team cadence management, dependency and risk tracking, and delivery transparency to the customer. • Ensure all teams can participate fully in agile practices, including two-week sprint delivery, quarterly Program Increment planning, backlog refinement, sprint planning, daily coordination, demos, retrospectives, and cross-team coordination forums. • Coordinate with product, architecture, engineering, data, security, AI, analytics, and user success leaders to align team backlogs with PI objectives, roadmap priorities, delivery constraints, and customer decision needs. • Maintain visibility into delivery flow, program risks, dependencies, impediments, decisions, and delivery health using customer-approved work management, documentation, collaboration, source control, and dashboarding tools. • Support routine reporting of delivery and product metrics, including deployment frequency, lead time to change, mean time to restore, change failure rate, burndown, sprint performance, PI performance, velocity, deliverable timeliness, and deliverable quality. • Facilitate regular demonstrations of working software, operational improvements, research findings, documentation improvements, dashboards, APIs, AI capabilities, and other demonstrable progress. • Promote blameless retrospectives and continuous improvement across delivery quality, service quality, collaboration, supportability, operational resilience, testing, and release readiness. • Lead agile coordination for applicable coverage areas, including cross-cutting program leadership, product management, engineering operations, architecture coordination, data operations, user success, support operations, and participation across all delivery workstreams.
Title: Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated) Location: New Haven United States Job Description: Join IQVIA's Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA's global expertise. Core Function Description: This role will support the Inflammation, Real World Evidence team, providing scientific and strategic epidemiology support for clinical development and drug safety activities. This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle. Key responsibilities include designing and conducting observational research studies, assessing evidence gaps, evaluating safety profiles, and developing evidence strategies to support regulatory interactions and clinical development programs. The Senior Epidemiologist will collaborate closely with cross-functional teams, including Clinical Development, Safety, Regulatory Affairs, Biostatistics, and Real-World Evidence stakeholders, to ensure appropriate epidemiologic approaches are applied to address critical business and scientific questions. The ideal candidate will have deep expertise in epidemiologic methods, demonstrated experience working within pharma or biotech, and a thorough understanding of regulatory requirements related to clinical development and safety evidence generation. This is a fully remote position based in the United States. Minimum Qualifications - Doctoral degree (PhD, ScD, or equivalent) in Epidemiology. - 5 to 7 years of epidemiology experience within a pharmaceutical/biotechnology company. - Demonstrated experience supporting clinical development and/or drug safety. - Strong expertise in observational research methods and the use of commercial healthcare databases such as HealthVerity, Pharmetrics Plus, TriNetX, or similar real-world data assets. - Solid understanding of regulatory requirements and evidence needs supporting clinical development, including the generation of evidence to address regulatory questions related to safety profiles and evidence gaps for Phase II and Phase III programs. - Proven ability to design, execute, and interpret epidemiologic studies that support regulatory, clinical, or safety objectives. Preferred Qualifications - Experience in Inflammation and Immunology therapeutic areas. - Knowledge of disease areas such as Atopic Dermatitis, Asthma, Lupus, Immune Thrombocytopenia (ITP), Autoimmune Hemolytic Anemia, or other immune-mediated diseases. - Experience supporting assets within emerging immunology programs. - Experience working with primary or hybrid real-world data sources in addition to secondary data sources. - Prior experience supporting regulatory submissions or interactions with FDA, EMA, or other global health authorities. What's in it for you? - Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare. - Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies. - Access IQVIA's global network who supports your growth. This is your chance to make an impact, while building a career that matters. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $109,200.00 - $273,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
Title: Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated) Locations: United States of America | Full time | Remote | R1554540 Job Description: Join IQVIA's Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA's global expertise. Core Function Description: This role will support the Inflammation, Real World Evidence team, providing scientific and strategic epidemiology support for clinical development and drug safety activities. This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle. Key responsibilities include designing and conducting observational research studies, assessing evidence gaps, evaluating safety profiles, and developing evidence strategies to support regulatory interactions and clinical development programs. The Senior Epidemiologist will collaborate closely with cross-functional teams, including Clinical Development, Safety, Regulatory Affairs, Biostatistics, and Real-World Evidence stakeholders, to ensure appropriate epidemiologic approaches are applied to address critical business and scientific questions. The ideal candidate will have deep expertise in epidemiologic methods, demonstrated experience working within pharma or biotech, and a thorough understanding of regulatory requirements related to clinical development and safety evidence generation. This is a fully remote position based in the United States. Minimum Qualifications - Doctoral degree (PhD, ScD, or equivalent) in Epidemiology. - 5 to 7 years of epidemiology experience within a pharmaceutical/biotechnology company. - Demonstrated experience supporting clinical development and/or drug safety. - Strong expertise in observational research methods and the use of commercial healthcare databases such as HealthVerity, Pharmetrics Plus, TriNetX, or similar real-world data assets. - Solid understanding of regulatory requirements and evidence needs supporting clinical development, including the generation of evidence to address regulatory questions related to safety profiles and evidence gaps for Phase II and Phase III programs. - Proven ability to design, execute, and interpret epidemiologic studies that support regulatory, clinical, or safety objectives. Preferred Qualifications - Experience in Inflammation and Immunology therapeutic areas. - Knowledge of disease areas such as Atopic Dermatitis, Asthma, Lupus, Immune Thrombocytopenia (ITP), Autoimmune Hemolytic Anemia, or other immune-mediated diseases. - Experience supporting assets within emerging immunology programs. - Experience working with primary or hybrid real-world data sources in addition to secondary data sources. - Prior experience supporting regulatory submissions or interactions with FDA, EMA, or other global health authorities. What's in it for you? - Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare. - Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies. - Access IQVIA's global network who supports your growth. This is your chance to make an impact, while building a career that matters. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide The potential base pay range for this role, when annualized, is $109,200.00 - $273,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
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