This page tracks remote principal openings that are location-eligible for Michigan.
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57 Jobs
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• 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
• 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.
IQVIA is a publicly-traded healthcare intelligence company founded in 2016 upon the merger of two market leaders: Quintiles and IMS Health. With locations aroun
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.
IQVIA is a publicly-traded healthcare intelligence company founded in 2016 upon the merger of two market leaders: Quintiles and IMS Health. With locations aroun
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.
United in our mission to accelerate the transition to 100% clean energy.
• Develop and execute strategies and campaigns to accelerate clean energy deployment in the MISO and SPP regions. • Draft comments and create reports, presentations, fact sheets, and other written and visual materials needed for education and advocacy efforts, and deliver verbal presentations as necessary. • Manage the tracking and analysis of MISO and SPP wholesale market reform efforts and planning processes, providing intelligence and insights for members and policymakers. • Develop and maintain excellent working relationships with United staff, members, partners, regulators and policymakers, and key wholesale electricity markets staff and market participants. • Work with United’s communications team to identify opportunities for United to seek earned media coverage, including op-eds, editorial board meetings, etc., in key media outlets. • Engage in coordination and advocacy efforts with coalition allies in support of clean energy goals in MISO and SPP.
Airbnb is a community based on connection and belonging.
• Competitive Monitoring: Develop and manage regular reporting to review key metrics across marketplace and product; track developing news and industry trends; lead monthly leadership insights forum • Strategic Deep Dives: Partner with key stakeholders across Supply, Global Markets, Product, and Marketing to conduct deep dives that will inform key decisions • Data Strategy: Lead the competitive intelligence data strategy — evaluate data required to achieve key growth initiatives and potential data sources; own relationships with external data providers and research vendors • Cross-Functional Enablement: Ensure competitive insights and datasets are accessible and actionable for XFN teams; partner with Engineering and Data teams to deliver reliable reporting infrastructure
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