Data Science Program Lead Ii jobs in Irvine – Browse 166 openings on RoboApply Jobs

Data Science Program Lead Ii jobs in Irvine

Open roles matching “Data Science Program Lead Ii” with location signals for Irvine. 166 active listings on RoboApply Jobs.

166 jobs found

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AbbVie Inc. logoAbbVie Inc. logo
Full-time|On-site|Irvine

Join AbbVie as a Data Science Program Lead II, where you will spearhead innovative data science projects that drive critical business decisions. In this role, you'll collaborate with cross-functional teams, leveraging advanced analytics to uncover insights and enhance operational effectiveness.

Apr 29, 2026
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AbbVie Inc. logoAbbVie Inc. logo
Full-time|On-site|Irvine

Join AbbVie as a Data Science Program Lead II, where you will spearhead innovative data-driven projects that transform the healthcare landscape. As a key member of our team, you will leverage your expertise in data science to lead and mentor a team, guiding them to deliver impactful insights and solutions. Your role will involve collaboration with cross-functional teams to enhance our decision-making capabilities and improve patient outcomes.

Apr 30, 2026
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AbbVie Inc. logoAbbVie Inc. logo
Full-time|On-site|Irvine

Join AbbVie as a Data Science Program Lead I, where you will spearhead innovative data science initiatives that drive impactful business decisions. In this role, you will collaborate with cross-functional teams to develop advanced analytics solutions, leveraging your expertise in data modeling, statistical analysis, and machine learning to enhance our products and services.

Apr 30, 2026
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AbbVie logoAbbVie logo
Full-time|On-site|Irvine

Join AbbVie as a Data Science Program Lead I, where you will be at the forefront of data-driven decision-making. In this dynamic role, you will lead data science initiatives, leveraging advanced analytics to provide insights that drive business strategies. Collaborate with cross-functional teams to enhance data accuracy and develop innovative solutions.

Apr 30, 2026
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AbbVie Inc. logoAbbVie Inc. logo
Full-time|On-site|Irvine

Join AbbVie as a Data Science Program Lead I and play a critical role in driving innovative data science initiatives. You will lead projects, collaborate with cross-functional teams, and utilize your analytical skills to enhance our data-driven decision-making processes. This position offers a unique opportunity to contribute to impactful projects within a dynamic team.

Apr 29, 2026
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AbbVie logoAbbVie logo
Full-time|On-site|Irvine

Join AbbVie as a Senior Scientist II / Principal Research Scientist I in our innovative Translational Program Science team. We are seeking passionate and experienced scientists to drive impactful research initiatives that bridge the gap between laboratory discoveries and clinical applications. This role involves leading research projects, collaborating with cross-functional teams, and contributing to the development of cutting-edge therapies.

Apr 30, 2026
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AbbVie Inc. logoAbbVie Inc. logo
Full-time|On-site|Irvine

Join AbbVie, a global biopharmaceutical company that combines advanced science with a passion for improving patients' lives. We are seeking a dedicated and experienced Senior Scientist II / Principal Research Scientist I to lead our Translational Program Science team in Irvine, California. This role is pivotal in bridging laboratory research with clinical application, focusing on the development and execution of innovative strategies to translate findings into therapeutic options.

May 1, 2026
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AbbVie Inc. logoAbbVie Inc. logo
Full-time|On-site|Irvine

Join AbbVie, a global biopharmaceutical company committed to innovation and the advancement of healthcare. We are seeking a talented and experienced Senior Scientist II/Principal Research Scientist I in our Translational Program Science team. In this role, you will leverage your expertise to translate complex scientific concepts into transformative therapeutic strategies. Collaborate with cross-functional teams to drive research initiatives and contribute to the development of novel therapies.

Apr 30, 2026
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Stanbridge University logoStanbridge University logo
Full-time|On-site|Irvine, California, United States

Assistant Program Director for Bachelor of Science in NursingStanbridge University is on the lookout for a dedicated and experienced Assistant Program Director to join our Bachelor of Science in Nursing (BSN) Program team. This pivotal role, reporting directly to the Program Director, is crucial in steering program operations, enhancing faculty performance, executing curriculum implementation, and elevating student outcomes.The Assistant Program Director will be instrumental in upholding academic excellence, ensuring regulatory compliance, and fostering a robust learning environment for students. This position will directly impact faculty effectiveness and student success through informed decision-making based on data, proactive problem-solving, and an unwavering commitment to continuous program enhancement.This is a remarkable opportunity to become part of a well-respected and expanding institution that prioritizes innovation, student achievement, and academic distinction.Key ResponsibilitiesProgram Leadership & OperationsOversee daily operations of the BSN program, including advising students and supervising clinical education.Collaborate with the Program Director to ensure alignment with program objectives, institutional goals, and accreditation standards.Engage in ongoing program evaluation and enhancement through comprehensive data analysis and outcome monitoring.Faculty Leadership & DevelopmentAssist in the recruitment, onboarding, development, and assessment of faculty, adhering to institutional and accreditation standards.Guide faculty to promote effective teaching practices and foster student engagement.Encourage a culture of collaboration, accountability, and instructional excellence.Curriculum & Academic QualitySupport the development, implementation, and assessment of the curriculum in line with BRN and institutional standards.Facilitate shared governance processes related to curriculum modifications and enhancements.Ensure uniformity and quality across course delivery, clinical instruction, and learning outcomes.Student Success & OutcomesAssess student performance, progression, and program outcomes.Implement strategies to enhance retention, completion rates, and NCLEX exam performance.Encourage effective utilization of ATI resources and data-driven intervention strategies.Compliance & AccreditationEnsure compliance with institutional policies and accreditation mandates.Assist in the preparation of reports, documentation, and correspondence with accrediting bodies.Regularly review program materials and publications for compliance and accuracy.

Apr 13, 2026
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The Trade Desk logoThe Trade Desk logo
Applied Scientist II

The Trade Desk

Full-time|On-site|Irvine

Join The Trade Desk as an Applied Scientist II, where you will leverage your analytical skills to drive impactful data-driven decisions. In this role, you will collaborate with cross-functional teams to develop and implement advanced algorithms that enhance our advertising solutions. Your work will focus on transforming complex data into actionable insights, contributing to the innovation of our platform.

Apr 8, 2026
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itcss logoitcss logo
Full-time|$120K/yr - $168K/yr|On-site|Irvine, California, United States

Hello Tarsan!We appreciate your interest in the Manager II, Compliance position. Please take a moment to examine the details below. If this role aligns with your career aspirations, we encourage you to discuss your qualifications with your current manager and HR business partner. If everything aligns, we invite you to apply, and our Talent Acquisition team will reach out to schedule an interview, allowing us to get to know you better.- Your Human Resources TeamAbout the RoleThe Manager II, Compliance will collaborate closely with the Compliance Department to design, implement, and uphold a robust Compliance Program that fosters a company-wide culture of ethics and compliance while adhering to regulatory requirements. This includes compliance with the Office of Inspector General (OIG) Guidance, the U.S. Sentencing Guidelines, and Department of Justice guidance. As part of a dynamic team, you will play a vital role in shaping and sustaining all components of the Tarsus Compliance program.Key Responsibilities:Lead the end-to-end transparency reporting process, ensuring compliance with federal and state reporting obligations. Collaborate with internal stakeholders for accurate data collection, manage external vendor relationships, deliver training, and maintain systems for timely and compliant submissions.Oversee compliance with federal and state healthcare laws and regulations. Monitor regulatory developments and partner with internal teams to assess impacts, implement controls, and ensure alignment with company policies.Develop and maintain reporting tools, dashboards, and data outputs related to transparency reporting and compliance processes, ensuring data quality and accuracy. Collaborate with the Compliance Data Analytics Lead to support analytics initiatives and explore opportunities to utilize data analytics and emerging technologies for process enhancement and operational efficiency.Manage relationships with external vendors supporting transparency reporting systems, focusing on data quality and performance improvements.Assist the Compliance Officer with additional projects and tasks as required.Salary Range: $120,000 - $168,000

Mar 24, 2026
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itcss logoitcss logo
Full-time|$120K/yr - $168K/yr|On-site|Irvine, California, United States

Hello, and thank you for your interest in the Quality Compliance Manager II position at itcss! We encourage you to review the details below. If this role aligns with your career aspirations, please discuss with your current manager and HR business partner to see if your qualifications match. If all goes well, we invite you to apply, and our Talent Acquisition team will reach out for an interview to learn more about you.- Your Human Resources TeamAbout the Role:The Quality Compliance Manager II plays a crucial role in supporting the Product Quality Complaint program, ensuring all complaints are addressed in compliance with Good Manufacturing Practices (GMPs) and health authority regulations. This position will also support Annual Product Reviews and assist in various Quality Management System (QMS) areas as needed, such as audits, inspections, change control, document control, and corrective action and preventive action (CAPA).Key Responsibilities:Manage the product complaint program throughout its lifecycle, including:Initiating Product Complaint InvestigationsCollaborating with Call Center staff for complaint intakeFollowing up with complainants as neededParticipating in Weekly Product Complaint MeetingsDrafting response letters to complainantsReviewing and closing Product Complaint investigationsContributing data to Annual Product ReviewsPreparing monthly metrics and management presentationsSupporting regulatory inspections or partner audits as necessaryAuthoring, revising, or approving controlled documentsStay abreast of regulatory changes and proactively adjust systems and procedures to ensure compliance with company policies and regulations.Monitor and escalate product complaints appropriately, including expedited complaints.Foster strong relationships, cooperation, and alignment with internal Quality partners.Compile Annual Product Reviews, ensuring timely data submission from collaborating departments.Assist with product recalls or field alerts as needed.

Mar 31, 2026
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itcss logoitcss logo
Full-time|$134.2K/yr - $188K/yr|On-site|Irvine, California, United States

Hello Tarsan,Thank you for your interest in this exciting opportunity! We encourage you to review the details below. If this role aligns with your career aspirations, we recommend connecting with your current manager and HR Business Partner to discuss how your skills and experiences match. If all is well, please submit your application, and our Talent Acquisition team will reach out to arrange an interview to learn more about you.- Your Human Resources TeamAbout the PositionWe are seeking a dedicated Manager II for Scientific & Medical Communications to spearhead our medical communications initiatives. You will report directly to the Senior Director of Scientific and Medical Communications and will collaborate extensively across all medical affairs functions. We are looking for a detail-oriented individual with exceptional project management skills who is analytical, innovative, and enjoys creating scientific content.Key ResponsibilitiesDesign and execute medical communication strategies, working collaboratively with cross-functional teams to ensure consistent messaging.Develop, review, and finalize external-facing medical content and educational resources in accordance with the medical communication strategy.Assist in generating posters and presentations for conferences both domestically and internationally.Oversee publication projects, including editorial assistance, article writing, quality assurance, and coordination of submission processes.Provide training and education on posters and presentations for medical congresses.Support medical information, congress activities, and advisory board initiatives.Manage project-related tasks concerning internal contracting and content review processes, including contracting and MLR.

Feb 17, 2026
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Tarsus Pharmaceuticals, Inc. logoTarsus Pharmaceuticals, Inc. logo
Manager II, Clinical Quality Assurance

Tarsus Pharmaceuticals, Inc.

Full-time|$120K/yr - $168K/yr|On-site|Irvine, California, United States

About the Role As a pivotal member of the Clinical Quality Assurance team, reporting directly to the Director of Clinical Quality Assurance, the Manager II will spearhead clinical quality support and the management of our comprehensive supplier qualification programs encompassing Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Pharmacovigilance Practice (GVP). The ideal candidate will play a crucial role in ensuring inspection readiness across the organization, providing training and guidance to maintain compliance with the latest ICH GCP E6 standards and relevant regulations. Key Responsibilities: Deliver daily clinical quality support and training to uphold adherence to regulatory requirements, company policies, and procedures. Oversee internal and supplier audits related to GCP/GLP/GVP, including the management of the audit schedule within the Quality Management System (QMS). Conduct supplier audits and prepare comprehensive reports as necessary. Compile responses to audits and assess evidence of implementation. Assist in the development and execution of quality systems and processes within the Clinical Quality domain. Review and approve QMS records for completeness and compliance with SOPs and regulations. Support the development of remediation plans and monitor the resolution of quality issues. Contribute to the review of Clinical Quality Management Plans (CQMPs) for clinical trials and vendor performance. Manage and enhance clinical training curricula. Support the creation of tracking tools for reporting quality metrics. Conduct and review Risk Assessments as required. Collaborate closely with Quality Management to ensure compliance with all applicable guidelines and SOPs. Act as a resource for Clinical Development, Operations, and Quality teams.

Mar 30, 2026
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Leverdemo-8 logo
Full-time|On-site|Irvine, CA

Join our innovative team at Lever as a Senior Data Scientist in Irvine, CA! We are on a mission to redefine the recruitment landscape by developing cutting-edge hiring software used by industry giants such as Netflix, Shopify, and Spotify.Lever, recognized as the #1 workplace in San Francisco, is committed to nurturing its employees and fostering a people-first culture. As we continue to scale our operations, we seek talented individuals who are eager to contribute to our success.As part of the Product team, the Senior Data Scientist will leverage data-driven insights to enhance our software solutions and improve user experiences.

Nov 27, 2019
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Tarsus Pharmaceuticals, Inc. logoTarsus Pharmaceuticals, Inc. logo
Full-time|On-site|Irvine, California, United States

The Associate Director of Translational Science at Tarsus Pharmaceuticals, Inc. will lead research efforts aimed at developing new therapies. Based in Irvine, California, this position plays a key role in moving scientific discoveries from the lab toward clinical use. The role involves frequent collaboration with teams across the organization to ensure research aligns with broader company objectives. Key responsibilities Direct translational research projects, guiding them from initial planning through completion Work closely with colleagues in various departments to coordinate research activities with company priorities Share updates on project progress and scientific results with stakeholders in a clear and timely manner Make sure all research supports the organization’s strategic goals

Apr 27, 2026
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Compa logoCompa logo
Full-time|Hybrid|Orange County HQ

About CompaCompa is an innovative, venture-backed AI startup that is transforming the landscape of compensation management.In today's fast-paced job market, companies face hiring challenges, the need for accountability, and the emergence of AI technologies. To navigate these complexities, organizations require accurate and timely data. Compa's cutting-edge real-time compensation data platform equips enterprise teams with unparalleled compensation intelligence.As a leader in compensation intelligence, Compa is dedicated to enhancing the capabilities of enterprise compensation teams in the AI era.Our esteemed clientele includes industry giants such as NVIDIA, Stripe, DoorDash, OpenAI, T-Mobile, Moderna, Workday, Ulta, Target, and more.Company Locations:Compa's headquarters are situated in Irvine, California, with additional offices in Denver, Colorado, and San Francisco, California. We pride ourselves on fostering a collaborative, inquisitive, and results-driven team culture that emphasizes transparency, personal accountability, and ongoing professional development, while valuing in-person collaboration whenever possible.Work Location: Irvine, CA (hybrid) or remote from San Francisco, CA.The Role:We are on the lookout for an Innovation Program Manager to spearhead our customer collaboration initiatives and help define the future of compensation intelligence. In this pivotal role, you will design and oversee structured customer programs aimed at extracting insights, validating concepts, and expediting product development. You will work closely with teams across Product, Compensation, Sales, and Marketing to convert customer feedback into impactful business outcomes. This position demands exceptional facilitation skills, strategic foresight, and a strong customer-centric approach.Key ResponsibilitiesDesign and facilitate Design Partner Programs with enterprise clientsConduct customer research studies to derive insights and validate product trajectoriesCollaborate with Product teams to distill research findings into actionable product specificationsCreate customer enablement content, resources, and program documentationEngage with Product and Compensation teams to establish and achieve program goalsAssist Sales with insights and engagement strategies to drive deal closurePartner with Marketing to produce customer case studies and showcase program impacts

Dec 9, 2025
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Tarsus Pharmaceuticals, Inc. logoTarsus Pharmaceuticals, Inc. logo
Full-time|$150K/yr - $210K/yr|On-site|Irvine, California, United States

The Associate Director of Translational Science at Tarsus Pharmaceuticals, Inc. helps shape the company’s research pipeline by connecting scientific discovery with clinical development. This position blends expertise in biology and pharmacology with a strategic approach to move projects from early-stage concepts through IND-enabling studies. The role works across teams to bridge translational medicine and product development efforts. Main responsibilities Act as a subject matter expert in pharmacology, pathophysiology, and drug discovery. Develop and maintain relationships with key opinion leaders, academic partners, and external collaborators. Collaborate with internal groups, such as the Innovation Lab and Business Development, to support asset evaluation and IND development strategies. Lead preclinical strategy, including animal model selection, study design, and coordination with external CROs to demonstrate proof of concept, pharmacokinetics, pharmacodynamics, and dose selection. Shape project strategies for pipeline programs, focusing on asset differentiation and guiding critical Go/No Go decisions to address unmet medical needs. Translational biology and pharmacology Build internal expertise in prioritized ophthalmology disease areas, covering mechanisms, disease models, and approaches for preclinical proof of concept. Develop and test translational hypotheses to address unmet needs, including mechanism of action, pharmacodynamics, and patient selection. Evaluate relevant models and work with CROs and academic experts to assess potential assets. Innovation and external assessment Partner with Business Development to provide scientific input on external asset assessment and prioritization of new opportunities. Location This position is based in Irvine, California, United States.

Apr 27, 2026
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Tarsus Pharmaceuticals, Inc. logoTarsus Pharmaceuticals, Inc. logo
Associate Director of Clinical Science

Tarsus Pharmaceuticals, Inc.

Full-time|On-site|Irvine, California, United States

Tarsus Pharmaceuticals, Inc., is seeking an experienced Associate Director of Clinical Science to lead our clinical development efforts. The ideal candidate will have a strong background in clinical research, particularly in the field of ophthalmology, and a proven track record of successful trial management.In this role, you will be responsible for designing and overseeing clinical trials, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to drive project success. Strong leadership skills and the ability to communicate effectively with stakeholders at all levels are essential.

Apr 30, 2026
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Twitch Interactive, Inc. logoTwitch Interactive, Inc. logo
Full-time|$129.5K/yr - $192.6K/yr|On-site|Irvine, CA; New York City; San Francisco, CA; Seattle, WA

About UsTwitch is the largest live streaming platform globally, fostering vibrant communities around gaming, entertainment, music, sports, cooking, and more. Every day, thousands of communities unite to share their passions.We are dedicated to community collaboration. Our team members are enthusiastic about teamwork, innovation, and problem-solving. If you’re passionate about empowering live communities, we invite you to explore our initiatives on LinkedIn, X, and our Blog. Don’t forget to check out our Interviewing Guide to prepare for our hiring process.

Apr 8, 2026

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