Head of Global Regulatory Affairs (U.S. Remote) Adagene IncorporatedHead of Global Regulatory Affairs (U.S. Remote)San Diego, CARemoteMust have extensive knowledge of regulatory requirements, including ICH GCP, GMP, GLP, and regional requirements and understand current global and regional trends in regulatory affairs and the ability to assess the impact of these requirements to the business. As a Head of Global Regulatory Affairs this person will perform a critical role in strategies, documentations, submissions, and company interactions to regulatory authorities such as FDA, CFDA, and other regulatory agencies.
Director of Regulatory & Tech Transfer Kitsch LLCDirector of Regulatory & Tech TransferLos Angeles, CARemoteJob Responsibilities Produce a complete supply risk map of every active SKU in Haircare, Body, and Fragrance within your first 90 days, ranking each by vulnerability; qualify and validate at least one alternative supplier for every high-risk SKU within 12 months. As Director of Regulatory & Tech Transfer, you will own the regulatory and supply infrastructure that keeps every Consumables SKU across Haircare, Body, and Fragrance compliant, quality-certified, and never dependent on a single source.
Project Manager - Regulatory And Licensing Stanford Health CareProject Manager - Regulatory And LicensingPalo Alto, CA$62.75–$83.16 / hourProject Managers are responsible for the coordination and completion of all aspects of project management on assigned projects, including, but not limited to, project scope, project schedule, project budget, project plans, facilitating meetings, documenting requirements, overseeing development, operational workflows, and implementation. As a Project Manager- Regulatory & Licensing, you'll manage the licensing and regulatory coordination for healthcare projects, partnering closely with internal medical planning and regulatory affairs teams, external design teams, and authorities having jurisdiction.
Senior Regulatory Advisor California Resources CorpSenior Regulatory AdvisorBakersfield, CAResponsibilities: Permitting Strategy and Execution: Lead, direct and manage the permitting process for CTV projects, including developing permitting strategies, identifying required approvals, and ensuring timely acquisition of all permits and authorizations. This role is responsible for driving successful permitting outcomes by coordinating across regulatory agencies, internal teams, and external stakeholders, while ensuring full compliance with applicable local, state, and federal requirements.
Senior Managing Regulatory Scientist Exponent IncSenior Managing Regulatory ScientistMenlo Park, CA$174,000–$213,000 / yearIn this role you will work as part of a team to to utilize your experience and skills related to (1) nutrition (with an emphasis on animal feed), food ingredients, manufacturing process procedures, (2) ensuring current regulatory compliance requirements and industry best practices associated with food, beverages, and nutritional products (human and animals), (3) food defense related issues. For over five decades, we''ve connected the lessons of past failures with tomorrow''s solutions to advise clients as they innovate technologically complex products and processes, ensure the safety and health of their users, and address the challenges of sustainability.
NewDirector (Public Sector Consulting - Regulatory Compliance & Grants) Macias Gini & O'Connell, LLPDirector (Public Sector Consulting - Regulatory Compliance & Grants)Walnut Creek, CARemoteThis leadership role serves state and local governments, public agencies, higher education institutions, nonprofits, and other organizations receiving public funding. The Director will serve as a trusted advisor to executive leaders, providing strategic guidance on regulatory compliance, federal and state funding requirements, governance, risk management, internal controls, and grants administration.
Project Manager - Regulatory and Licensing Stanford Health CareProject Manager - Regulatory and LicensingPalo Alto, CaliforniaProject Managers are responsible for the coordination and completion of all aspects of project management on assigned projects, including, but not limited to, project scope, project schedule, project budget, project plans, facilitating meetings, documenting requirements, overseeing development, operational workflows, and implementation. As a Project Manager - Regulatory & Licensing, you’ll manage the licensing and regulatory coordination for healthcare projects, partnering closely with internal medical planning and regulatory affairs teams, external design teams, and authorities having jurisdiction.
Senior Regulatory Advisor California Resources CorporationSenior Regulatory AdvisorBakersfield, CAResponsibilities: Permitting Strategy and Execution: Lead, direct and manage the permitting process for CTV projects, including developing permitting strategies, identifying required approvals, and ensuring timely acquisition of all permits and authorizations. This role is responsible for driving successful permitting outcomes by coordinating across regulatory agencies, internal teams, and external stakeholders, while ensuring full compliance with applicable local, state, and federal requirements.
NewPUBLIC UTILITIES REGULATORY ANALYST III State Of CaliforniaPUBLIC UTILITIES REGULATORY ANALYST IIISan Francisco, CA$7,980–$9,994Under general direction of the Program and Project Supervisor, the person who fills this position will work on issues related to Core Transport Agents (CTAs) who are non-utility natural gas providers who sell the fuel to customers while the utility delivers it to them. Applicants who completed their education outside the United States (with foreign degrees/transcripts) must obtain and submit verification of United States course/degree equivalency by the application deadline.
Regulatory Coordinator Actalent IncRegulatory CoordinatorFountain Valley, CA$28–$30 / hourWorking closely with Clinical Research Coordinators and the Regulatory Coordinator, this position ensures that all study records are complete, compliant, and audit-ready in alignment with GCP, FDA regulations, and study protocols. This role is ideal for a detail-oriented clinical research professional who thrives in a fast-paced, high-volume research environment and enjoys contributing directly to the quality and integrity of clinical trial data.
Manager, Regulatory and Market Affairs Pattern Energy Group LPManager, Regulatory and Market AffairsSan Francisco, California$103,000–$138,000 / yearA key function of this role will be to identify, research, analyze, and synthesize the cross section of regulatory and wholesale market rules impacting Pattern’s existing and planned assets in WECC, MISO, ERCOT, SPP, PJM and other priority markets as needed. Importantly, the role will support the coordination with expert consultants and internal SMEs to clearly and regularly identify and lead Pattern’s engagement in regulatory and market design changes, develop Pattern’s positions and execute on strategies to achieve desired objectives.
Regulatory Reporting Manager Deloitte Touche Tohmatsu LtdRegulatory Reporting ManagerFresno, CA$82,600–$162,800 / yearManage end to end regulatory reporting activities covering 40 Act and non-40 Act funds in the investment management space (e.g., Form PF, TIC, CPO-PQR, Form 16, Form 13, N-PX, BEA reports), ensuring compliance with applicable regulatory requirements across various regulators such as SEC, CFTC, BEA, NFA, Treasury. We "embed continuous advantage" through domain, industry, technology and transformation skills to perform client business functions that manage risk and deliver value-added outcomes, all while driving predictable long-term revenue, profitability, and growth.
Regulatory & Permitting Lead Ambrosia EnergyRegulatory & Permitting LeadRedwood City, CaliforniaLead all permitting activities for solar and battery storage projects in Texas and other target states, including local land use, zoning, conditional use permits, and environmental approvals. As global energy demand surges—driven by the rapid rise of data centers, electric vehicles, and future in-home robotics—the world stands at a critical energy inflection point.
Regulatory Assistant StratAcuity Staffing Partners IncRegulatory AssistantBurlingame, CA$50–$55 / hourIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Everforth Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts.
Manager, Regulatory and Market Affairs Pattern Energy Group IncManager, Regulatory and Market AffairsSan Francisco, CA$103,000–$138,000 / yearA key function of this role will be to identify, research, analyze, and synthesize the cross section of regulatory and wholesale market rules impacting Pattern's existing and planned assets in WECC, MISO, ERCOT, SPP, PJM and other priority markets as needed. Importantly, the role will support the coordination with expert consultants and internal SMEs to clearly and regularly identify and lead Pattern's engagement in regulatory and market design changes, develop Pattern's positions and execute on strategies to achieve desired objectives.
Director, Regulatory Affairs Premier Research International LLCDirector, Regulatory AffairsSan Francisco, CAExpert in the drug development process with experience in multiple phases (early and late stage, post-approval) in various therapeutic areas and product types (drugs, biologics, drug-drug combinations, drug-device combination products). Provide efficient and effective regulatory representation with clients as well as across the organization and act as a key player in interactions with the Food and Drug Administration (FDA) and other regulatory agencies.
Sr. Regulatory Compliance Engineer, Safety Tesla IncSr. Regulatory Compliance Engineer, SafetyFremont, CA$96,000–$222,000 / yearIEC 62619, UN 38.3, IEC 62109-1, IEC 62109-2, IEC 62933-5-2, IEC 62477-1, IEC 60730 Annex H, UL 9540, UL 9540A, UL 1973, UL 1741, UL 1699B(AFCI), UL 1998, UL 991, ANSI C12.1, ANSI C12.20, IEC 62933-5-1, IEC 62933-5-2, IEC 62619, UN 38.3, IEC 62109-1, IEC 62109-2, IEC 62933-5-2, IEC 62477-1, IEC 60730 Annex. Collaborate with internal and external stakeholders to troubleshoot the EUT and prepare alternative solutions, negotiate testing scope and pass/fail criteria with NRTLs while meeting project timeline and safe work practices.
NewManager, Regulatory Affairs Noctrix HealthManager, Regulatory AffairsPleasanton, CA$150,000–$180,000 / yearThe Manager, Regulatory Affairs will work closely with Clinical Affairs, Quality, Engineering, Operations, Marketing, and external regulatory partners to provide regulatory guidance, manage submissions, assess product changes, maintain global registrations, and support post-market regulatory activities. We are seeking an experienced and highly organized Manager, Regulatory Affairs to lead and execute regulatory activities supporting the development, registration, commercialization, and post-market compliance of Noctrix Health's medical devices.
Sr. Regulatory Compliance Engineer, Grid Tesla IncSr. Regulatory Compliance Engineer, GridFremont, CA$96,000–$222,000 / yearVDE 4105, VDE 4100, VDE 0124, VDE 4110, VDE 4120, VDE 4130, CEI 0-21, C10/11, TOR Erzeuger, UL 9741, UL 1741 SC, SAE J3072, EU RFG, IEC 61851-1, ISO 15118-20. Collaborate with internal and external stakeholders to troubleshoot the EUT and prepare alternative solutions, negotiate testing scope and pass/fail criteria with NRTLs while meeting project timeline and safe work practices.
Regulatory Specialist IV Resource Environmental Solutions LLCRegulatory Specialist IVSacramento, CA$102,000–$125,000 / yearThis role is ideal for a senior regulatory professional who understands how to navigate complex agency requirements, prepare and review high-quality permit documents, evaluate project risk, and serve as a trusted technical resource for project teams, clients, and regulatory partners. The Regulatory Specialist IV will lead and support environmental permitting efforts across multiple project phases, from early feasibility and proposal support through project development, agency coordination, implementation, compliance, and closeout.
Sr. Regulatory Affairs Specialist - Ad/Promo Prolacta BioscienceSr. Regulatory Affairs Specialist - Ad/PromoDuarte, CA$112,000–$125,000Experience coordinating cross-functional reviews, resolving comments, maintaining trackers, preparing status updates, and supporting timely completion of review, approval, submission, and record-retention activities. Review assigned advertising, promotional, labeling, packaging, digital, scientific, educational, technical, and other external-facing materials for regulatory compliance, intended use, claim support, accuracy, balance, and consistency with approved source documents.
Accreditation and Regulatory Specialist, Clinical Salinas Valley HealthAccreditation and Regulatory Specialist, ClinicalSalinas, Californiathose agencies, including, but not limited to, the following: Serves as coordinator for all matters concerning the state licensure of SVH, works with SVH departments regarding pre-licensing inspections in the hospital and clinics, prepares and submits licensing applications and supplementary profile information when changes are brought about by the creation of new or remodeled patient care locations, change of beds, services, or administrators, new equipment, construction, and other changes that necessitate changes in the hospital license, inspection by CDPH, and special permits or variances. The Specialist works under the Director of Accreditation and Regulatory to assist in creating, implementing, and maintaining the strategy and tactics to ensure that SVH is continually prepared for Joint Commission accreditation, CDPH licensure, federal and state regulatory surveys, and compliance with all pertinent regulatory and accreditation requirements.
Regulatory Lead Actalent IncRegulatory LeadTorrance, CA$28–$36 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Director / Sr. Director, Regulatory Affairs (Strategy, Oncology Solid Tumors) Nurix Therapeutics, Inc.Director / Sr. Director, Regulatory Affairs (Strategy, Oncology Solid Tumors)Brisbane, CA$232,000–$274,000 / yearThis role will be responsible for developing and executing the global regulatory strategy in collaboration with key internal stakeholders, as well as tactical implementation of that strategy, guiding and executing compliant, high quality, nonclinical and clinical submissions and interactions in support of registration and life cycle management activities. Works strategically with all regulatory functions to develop detailed, actionable submission plans, tracks major submission deliverables, and ensures consistent management submission documents, health authority communications, and all other regulatory information supporting Nurix's investigational and marketing applications.
Senior Program Director, Commercial Regulatory Affairs SGA Inc.Senior Program Director, Commercial Regulatory AffairsSouth San Francisco, CAResponsibilities : Commercial Regulatory Affairs (CORA) is part that interprets the needs of worldwide health authorities and provides regulatory intelligence necessary to generate and present information that meets the needs of health authorities, patients, purchasers and prescribers for the firm's global Pharma Division, which includes all therapeutic areas and all phases of product development from early development to post marketing. Must demonstrate in-depth knowledge of the bio/pharma industry (compliance, legal, clinical affairs, regulatory and product marketing) as well as in-depth knowledge of the legal and regulatory environment, as it relates to healthcare compliance in the bio/pharma industry (includes anti-kickback statutes, government fraud & abuse, off-label promotion, PhRMA Code, etc.).
Director, Regulatory Affairs (Strategy, I&I) Nurix Therapeutics, Inc.Director, Regulatory Affairs (Strategy, I&I)Brisbane, CAThis role will be responsible for developing the global regulatory strategy in collaboration with key internal stakeholders, as well as tactical implementation of that strategy guiding and executing compliant, high quality, nonclinical and clinical submissions and interactions in support of early development, registration and life cycle management activities. Works strategically with all regulatory functions to develop detailed, actionable submission plans, tracks major submission deliverables, and ensures consistent management submission documents, health authority communications, and all other regulatory information supporting Nurix's investigational and marketing applications.
Associate Director, Global Regulatory Affairs Project Management Revolution Medicines, Inc.Associate Director, Global Regulatory Affairs Project ManagementRedwood City, CA$186,000–$233,000 / yearDrive the operational planning, coordination, and tracking of new drug marketing application submission activities across cross-functional Filing Teams (including Regulatory, Medical Writing, Nonclinical, Clinical, Safety, Biostatistics, CMC / Pharmaceutical Development and Manufacturing, etc. and external consultants), supporting the Global Filing Lead's strategic vision. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.
Director, Regulatory Affairs Calico Life Sciences LLCDirector, Regulatory AffairsSouth San Francisco, CA$275,000–$280,000 / yearPosition Responsibilities: Accountable to develop and execute the world-wide regulatory strategy for assigned programs (from IND-enabling to clinical proof-of-concept and beyond), which may include programs that are first-in-class, where no or limited FDA guidance exists, that have an external business partner, and where there are multiple indications. Calico's highly innovative technology labs, its commitment to curiosity-driven discovery science, and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs.
Director / Senior Director Of Regulatory Operations Artiva BiotherapeuticsDirector / Senior Director Of Regulatory OperationsSan Diego, CA$205,000–$268,000 / yearThe ideal candidate will bring deep expertise in eCTD submissions, regulatory information management systems, and cross-functional project leadership in a fast-paced biotech environment, with preference for experience in cell therapy or biologics. Partner with Regulatory Affairs Leads, Clinical Development, CMC, Pharmacovigilance, Project Management and Program Lead to develop and maintain integrated regulatory project plans, timelines, and risk mitigation strategies.
Vice President, Regulatory Affairs Sight Sciences IncVice President, Regulatory AffairsMenlo Park, CAProven leadership in compliance with an ability to troubleshoot within FDA and international regulations and guidelines including, but not limited to, clinical strategy, GCPs, GLPs, SOPs, submissions, product launch, labeling, advertising and promotion, product vigilance, and medical device reporting. He or she should know regulatory road maps for medical devices and preferably combination drug-device products, which will speed up the clinical trial cycle, the regulatory process and garner more government resources.
Senior Director, Regulatory Affairs Annexon IncSenior Director, Regulatory AffairsSan Francisco, CARemote$216,000–$241,000 / yearResponsibilities include: Provides regulatory leadership in support of the development, registration, and life-cycle management of Annexon products by collaborating cross-functionally with Clinical Development, Clinical Operations, Medical Affairs, CMC, and Quality to develop, coordinate, and implement global regulatory strategies and submissions, including CTAs, for new and ongoing clinical studies. Responsibilities include developing and driving regulatory strategies and detailed plans to meet company objectives, participating in program core teams and governance forums, and managing interactions with regulatory agencies to support development and registration strategies.
Senior Regulatory Counsel, Americas AirwallexSenior Regulatory Counsel, AmericasSan Francisco, CaliforniaBe responsible for handling regulatory legal issues relating to our business across the Americas, and for providing strategic advice to cross-functional stakeholders relating to our existing licenses/registrations and potential future licence applications in the region, to ensure Airwallex can successfully scale in the Americas. Powered by our unique combination of proprietary infrastructure and software, we empower over 250,000 businesses worldwide – including Brex, Navan, Qantas, SHEIN and many more – with fully integrated solutions to manage everything from business accounts, payments, spend management and treasury, to embedded finance at a global scale.
Senior Director, Regulatory Affairs Annexon, Inc.Senior Director, Regulatory AffairsSan Francisco, CARemote$265,000–$285,000 / yearResponsibilities include: Provides regulatory leadership in support of the development, registration, and life-cycle management of Annexon products by collaborating cross-functionally with Clinical Development, Clinical Operations, Medical Affairs, CMC, and Quality to develop, coordinate, and implement global regulatory strategies and submissions, including CTAs, for new and ongoing clinical studies. Responsibilities include developing and driving regulatory strategies and detailed plans to meet company objectives, participating in program core teams and governance forums, and managing interactions with regulatory agencies to support development and registration strategies.
Senior Director, Regulatory CMC Senti Biosciences IncSenior Director, Regulatory CMCSouth San Francisco, CA$245,000–$285,000 / yearProvide strategic CMC regulatory support, guidance and expertise, and act as the Regulatory Affairs primary point of contact to cross-functional teams including Pharmaceutical Development, Quality Assurance, Quality Control, contract organizations and consultants. Work across functional groups in identifying issues that may delay timelines, providing solutions to difficult technical/functional issues associated with specific projects, as well as support the resolution of issues that arise.
Senior Director, Regulatory CMC Senti Biosciences Inc.Senior Director, Regulatory CMCSouth San Francisco, CA$245,000–$285,000 / yearProvide strategic CMC regulatory support, guidance and expertise, and act as the Regulatory Affairs primary point of contact to cross-functional teams including Pharmaceutical Development, Quality Assurance, Quality Control, contract organizations and consultants. Work across functional groups in identifying issues that may delay timelines, providing solutions to difficult technical/functional issues associated with specific projects, as well as support the resolution of issues that arise.
["Risk Consultant","Risk Consultant"] Oliver Wyman["Risk Consultant","Risk Consultant"]Los AngelesUnder minimal direction of the Director, Risk & Loss Advisors, and taking into consideration the client's readiness and ability to consider expanded and/or alternate methods of managing their prevention and safety programs, the Risk Consultant will provide a wide range ofservices for clients to include developing and supporting strategies to enhance the client's risk management, accident prevention and safety programs. Train client staff on a myriad of safety topics; presenting to employees in a wide variety of settings to include professional office environments, construction sites, manufacturing, transportation and light industry locations such as warehouses.
Director / Senior Director of Regulatory Operations Artiva Biotherapeutics IncDirector / Senior Director of Regulatory OperationsSan Diego, CA$205,000–$268,000 / yearThe ideal candidate will bring deep expertise in eCTD submissions, regulatory information management systems, and cross-functional project leadership in a fast-paced biotech environment, with preference for experience in cell therapy or biologics. Partner with Regulatory Affairs Leads, Clinical Development, CMC, Pharmacovigilance, Project Management and Program Lead to develop and maintain integrated regulatory project plans, timelines, and risk mitigation strategies.
Senior Compliance Consultant GTT, LLCSenior Compliance ConsultantOakland, CAOperating from a hub in Oakland, CA, the organization employs compliance analysts, regulatory specialists, engineers, data governance professionals, and systems analysts who collaborate across operations, regulatory affairs, and enterprise technology functions. This role conducts research and analysis of regulatory developments, maintains compliance documentation and tracking tools, and partners with cross-functional teams to translate external and internal requirements into clear business processes.
Medical Informatics Analyst, Consultant- Utilization Management Blue Cross and Blue Shield AssociationMedical Informatics Analyst, Consultant- Utilization ManagementRedding, CAThe Healthcare Quality Affordability (HQA) Analytics team plays a key role in discovering information hidden in vast amounts of data that can lead to smarter decisions and deliver better service for our customers and contain the rising cost of healthcare. Provide training and mentoring for team members on best practices for analysis and reporting; assist in the development of supplemental analytic training tools and materials; conducts formal training sessions for lower level analysts and analysts in other Departments.
NewCorporate Security and Safety Analyst, Consultant Blue Cross and Blue Shield AssociationCorporate Security and Safety Analyst, ConsultantOakland, CACollaborate cross-functionally with Threat Intelligence, HR, Legal, Cybersecurity, and Compliance teams to investigate and resolve incidents involving workplace violence, insider threats, external threats, and cyber-physical risks. The Corporate Security team is responsible for the safety and security of Blue Shield of California employees, visitors, and property including oversight of all elements of the Security Operations Center (SOC)/Security Fusion Center (SFC), safeguarding facilities, equipment, materials, and employee property.
Senior Statistical Programmer/Analyst Consultant Cardiovascular, Renal ClinChoice IncSenior Statistical Programmer/Analyst Consultant Cardiovascular, RenalCARemoteMain Job Tasks and Responsibilities: The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. Education and Experience: Bachelor's degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master's degree in CS, statistics or related disciplines with 6 yrs.
Electric NERC Compliance Consultant, Principal - Flexible Location PG&E CorpElectric NERC Compliance Consultant, Principal - Flexible LocationCAThe Electric NERC Compliance Consultant, Principal will lead collaboration with Electric Engineering, Asset management and Planning, and Electric Operations business units and the Enterprise NERC Compliance Office to guide mitigation planning, shaping risk-based decisions, aligning cross-functional partners, and influencing policy and regulatory strategy across WECC, FERC and CAISO. Develops and leads compelling data-driven business cases for or against specific courses of action and potential risk mitigation alternatives as appropriate; provides strategic direction regarding areas of NERC compliance in common with CPUC, OEIS, and CAISO.
(Agile1)Compliance Consultant, Senior Mindlance(Agile1)Compliance Consultant, SeniorOakland, CA$55–$60 / hourThis role conducts research and analysis of regulatory developments, maintains compliance documentation and tracking tools, and partners with cross-functional teams to translate external and internal requirements into clear business processes. TOPS THINGS LOOKING FOR: Engineering background preferred with a utility, regulatory compliance, policy implementation, cross-functional collaboration, data analysis, program management.
Principal Transportation & Energy Consultant (Port & Maritime Decarbonization) ICFPrincipal Transportation & Energy Consultant (Port & Maritime Decarbonization)Los Angeles, CaliforniaPay Range - There are multiple factors that are considered in determining final pay for a position, including, but not limited to, relevant work experience, skills, certifications and competencies that align to the specified role, geographic location, education and certifications as well as contract provisions regarding labor categories that are specific to the position. The consultant will support the development and implementation of strategies related to zero-emission cargo handling equipment, drayage truck charging infrastructure, shore power systems, battery storage, microgrids, and clean marine fuel deployment.
RN Clinical Consultant Titanium Healthcare IncRN Clinical ConsultantCARemoteAssociate's degree in nursing Minimum 1+ years of experience as an RN working in a healthcare setting, such as a medical clinic or acute care hospital A current and unrestricted CA state RN license Experience using an EHR Distraction-free home workspace with a secure internet connection. POSITION SUMMARY The RN Clinical Consultant is a key member of Titanium Healthcare's Enhanced Care Management (ECM) program, providing clinical oversight and guidance to support high-quality, coordinated care for complex member populations.
Principal Consultant, Security Governance Presidio IncPrincipal Consultant, Security GovernanceCARemotePresidios expert technical team develops custom applications, provides managed services, and enables actionable data insights and builds forward-thinking solutions that drive strategic outcomes for clients globally. Work with other seasoned Principal Security Consultants in a collaborative setting to support and assist on the execution and delivery of key services such as Cloud Governance, Advisory Services, security program development, documentation review, and security consulting services.
(Agile1)Compliance Consultant, Senior Abacus Service Corporation(Agile1)Compliance Consultant, SeniorOakland, CAYour responsibilities will include conducting research and analysis of regulatory developments, maintaining compliance documentation, and collaborating with cross-functional teams to ensure clear business processes. This hybrid role offers the perfect blend of in-office collaboration and remote work flexibility, with three days in the office and two days working from home each week.
Community Health Consultant V Kaiser PermanenteCommunity Health Consultant VSanta Cruz, CACreates communication strategies by: leading communications between KP and management in community agencies regarding health programs; guiding communication of KPs position and commitment to community health to internal and external audiences; guiding identification of corporate marketing, community relations outreach, and promoting media opportunities to increase visibility of community health portfolio and programs; creating and executing regular communication with internal and external stakeholders through regular reports and presentations as needed to communicate and integrate the impact of community and social health initiatives; guiding the development of communications to update programs, related stories, factsheets, press releases, and news articles; representing KP by initiating collaboratives, working groups, advisory boards, committees, panels, conferences, and planning groups; and educating and influencing community leaders by promoting KPs value and commitment to communities served. Leads community health program management by: leading community health programs in KPs Community Health Program, including assessing outcomes planning, design, and operations of initiatives that address community wellbeing and developing outcomes; guiding efforts to ensure that all community health programs and activities meet the needs of KPs diverse communities; assisting with development and managing implementation of community health strategies and programs across the market, including philanthropy, in-kind, and/or community health improvement programs at the local and/or market level; guiding, planning, and organizing the market-wide delivery of short and long range community initiatives and focus areas, ensuring alignment with community health priorities and organizational goals; and designing, developing, and implementing programs that measurably improve community health and support the organizations tax-exempt status.
Consultant IV Kaiser PermanenteConsultant IVOakland, CAServes as a consultant to ensure the alignment, buy-in, and coordination of diverse stakeholders to drive the implementation of successful business initiatives and projects across one or more functional tracks or workstreams by identifying and ensuring representation and inclusion of appropriate stakeholders; building rapport and partnerships with stakeholder teams, third party vendors, and senior management; working with stakeholders to develop goals and set the prioritization of deliverables; discussing involvement of business processes (e.g. Performs data analyses to support business initiatives by identifying appropriate data analysis tools and approach to assess business performance; determining suitable data gathering and analysis methods (e.g., process observation, hard data, etc.); defining data requirements and obtaining customer agreements, including customer requirements as appropriate; conducting analyses and performing experimental tests to evaluate the effectiveness of business solutions; and identifying and alleviating risks through data-driven analysis.
Compliance Consultant - Contract to Hire Western Alliance BancorpCompliance Consultant - Contract to HireIrvine, CA$114,910–$141,946 / yearAbility to assess compliance with applicable federal and state statutes (TILA, TRID, RESPA, ECOA, FCRA, HPA, FDPA, etc.), program specific requirements (ARM, DSCR, Interest Only, HELOC/HEL), and regulatory requirements circulated by agencies including FNMA, FHLMC, FHA, VA, USDA, and CFPB. What you'll do: As a Compliance Assistant Manager you''ll be a subject matter expert and provide advice, oversight and guidance related to regulatory compliance risks, control effectiveness, root cause analysis, and issue review and validation.