JouléNewDirector, Regulatory Affairs (Medical Devices) JouléDirector, Regulatory Affairs (Medical Devices)Denver, CO$195,500–$245,600 / yearA well-established and growth-oriented medical device organization is seeking a strategic regulatory leader to guide global regulatory affairs and labeling strategy across a diverse product portfolio. Required Experience:10+ years of progressive regulatory affairs experience within medical devices (combination product experience strongly preferred).
BP EnergyNewSenior GIS Specialist BP EnergySenior GIS SpecialistDenver, CO$128,000–$151,000Expert proficiency with Esri ArcGIS platform: ArcGIS Pro, ArcGIS Enterprise, Experience Builder, ArcGIS Field Maps, and ArcGIS Dashboards. Collaborate cross-functionally with operations, maintenance, construction, facility engineering, and project development teams to ensure GIS supports day-to-day decision-making.
Highridge IncRegulatory Affairs Specialist Highridge IncRegulatory Affairs SpecialistWestminster, COThis person will be joining a small, but mighty team and will have the opportunity to work on a variety of projects, focused on new product introduction, for the world's largest privately held spine company. Principal Duties and Responsibilities: Become a brand champion, owning regulatory activities for that brand, from new product introduction, to product changes and revisions, and international registration support.
MedtronicAssociate Regulatory Affairs Specialist MedtronicAssociate Regulatory Affairs SpecialistLafayette, ColoradoThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: 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, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find herea list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
MedtronicNewRegulatory Affairs Specialist - On-site MedtronicRegulatory Affairs Specialist - On-siteLafayette, ColoradoThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: 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, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find herea list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Medtronic PlcNewRegulatory Affairs Specialist - On-site Medtronic PlcRegulatory Affairs Specialist - On-siteLafayette, COThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: 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, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Stryker CorpSenior Regulatory Affairs Specialist Stryker CorpSenior Regulatory Affairs SpecialistGreenwood Village, COPreferred: • Bachelors degree in Regulatory Science, or technical discipline (Engineering or Life Sciences) • Experience engaging with regulatory authorities to support submissions, respond to inquiries, and facilitate successful interactions throughout the product lifecycle. In this role, you will develop and implement regulatory strategies, ensure compliance across the product lifecycle, manage regulatory submissions, advise stakeholders on regulatory requirements, and engage with regulatory authorities to resolve issues and support market access.
LivaNova PlcRegulatory & Clinical Specialist LivaNova PlcRegulatory & Clinical SpecialistDenver, CORemote$85,000–$95,000 / yearManage the overall development and approval process for assigned documents (CEP, CER, etc.) within timelines, including documentation generation, initiation of the review process, discussions on proposed revisions, and document completion in collaboration with other team members. The Regulatory and Clinical Specialist is a liaison with the organization working with various groups to effectively communicate and collaborate on the deliverables and meet the project deadlines in line with the regulatory requirements.
SM Energy CoEH&S Specialist - Regulatory SM Energy CoEH&S Specialist - RegulatoryDenver, COThis role ensures projects meet all applicable regulatory requirements by preparing and submitting permit applications, coordinating with internal teams, and maintaining accurate records throughout the permitting lifecycle. SM Energy offers competitive compensation and benefits programs which include, but are not limited to, variable pay, health care coverage, retirement plan, protection coverage, time off and leave programs, training and development opportunities and a range of allowances connected to specific work situations.
Suncor Energy IncSpecialist Environmental and Regulatory Advisor - Commerce City Suncor Energy IncSpecialist Environmental and Regulatory Advisor - Commerce CityCommerce City, CO$135,000–$157,000 / yearAs a Specialist Environmental and Regulatory Advisor you will support air permitting efforts, including Emission Inventories, support regulatory advocacy and implementation efforts including Environmental program development and management, and you will work with the Colorado Department of Public Health and the Environment (CDPHE). Responsibilities: Collect, assess, and manage environmental data to develop technical solutions that maximize compliance, performance, flexibility, and sustainability; maintain environmental databases, emissions calculations, inventories, and Annual Emissions Inventory Reports.
Vero NetworksRegulatory and Compliance Finance Specialist Vero NetworksRegulatory and Compliance Finance SpecialistDenver, ColoradoThis role serves as the central finance owner for VB-specific regulatory, payroll, and contract compliance, including USAC/FCC reporting, telecom sales and use tax compliance, tax engine and billing platform support, grant reporting and compliance, regulatory audits, and payroll-related regulatory filings. The Regulatory and Compliance Finance Specialist plays a critical role in mitigating regulatory, tax, payroll, and compliance risk for Vero Broadband, LLC (VB) and in supporting regulatory oversight across the broader Vero Fiber organization.
University of ColoradoRegulatory Affairs Supervisor University of ColoradoRegulatory Affairs SupervisorDenver, CO$71,517–$90,970 / yearInterpersonal Skills - Ability to establish and maintain effective working relationships with employees at all level; interacts with people in a friendly, open, honest manner; models a commitment to teamwork; demonstrates respect for the opinions of others; and maintains high level of confidentiality. The Regulatory Research Supervisor ensures regulatory compliance for clinical research studies, provides leadership and mentorship to regulatory personnel, and collaborates with investigators, sponsors, and research teams to support the timely and compliant conduct of clinical trials.
Medtronic PlcSr Regulatory Affairs Spec Medtronic PlcSr Regulatory Affairs SpecLafayette, COThis role will partner closely with Geography Regulatory Affairs to support international submissions, government queries, registration documentation, product approval and clearance activities, product demand and release planning, and post-market regulatory compliance to help ensure continued product availability worldwide. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: 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, and Simple Steps (global well-being program).
University of ColoradoRegulatory Affairs Coordinator (Open Rank: Senior-Principal) University of ColoradoRegulatory Affairs Coordinator (Open Rank: Senior-Principal)Denver, CO$59,995–$76,314 / yearPrimary duties will include, but not be limited to: submissions to the Institutional Review Board (IRB) of record including amendments, unanticipated problems, continuing reviews, and study closures; maintenance of the investigator site file/regulatory binder and all essential documents including documentation of appropriate training and delegation for all personnel; submissions to internal University and Hospital research portals; acting as primary regulatory contact person for sponsors/Contract Research Organizations (CROs)/coordinating centers; maintaining research credentials, training documentation and licenses; The Regulatory Affairs Coordinator will work closely with the Director of Clinical Research, program managers, and clinical research coordinators. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively.
Medtronic PlcSr Regulatory Affairs Manager Medtronic PlcSr Regulatory Affairs ManagerLafayette, CO$154,400–$231,600 / yearIf you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. As the Regulatory Affairs Manager, you will be responsible for establishing strategy for worldwide product approval submission activities, directly responsible for execution of submission activities focused on US/EU and for ensuring regulatory compliance for Acute Care and Monitoring products.
MedtronicNewPrin Regulatory Affairs Spec MedtronicPrin Regulatory Affairs SpecLafayette, ColoradoThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: 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, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find herea list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Medtronic PlcPrin Regulatory Affairs Spec Medtronic PlcPrin Regulatory Affairs SpecLafayette, COThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: 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, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Scout Clean Energy LLCManager, Government and Regulatory Affairs - PJM and MISO Scout Clean Energy LLCManager, Government and Regulatory Affairs - PJM and MISOBoulder, COThis individual will join a small team reporting to the Director, Government and Regulatory Affairs, and will coordinate closely with internal and external subject matter experts to advance Scout's policy strategy and support execution across the development and operating portfolio. Scout Clean Energy is seeking a motivated and collaborative Manager, Government and Regulatory Affairs to advance our legislative and regulatory priorities across assigned states within the MISO and PJM footprints.
Vensure Employer ServicesInternational Regulatory Affairs / Quality Assurance Associate - Louisville, CO. Vensure Employer ServicesInternational Regulatory Affairs / Quality Assurance Associate - Louisville, CO.Louisville, CODocumentation & Certificate Management Prepare documentation packages including Manufacturer's Declarations, Free Sale Certificates, GMP/ISO certifications, ingredient documents, specifications, and testing reports. This role is responsible for preparing, managing, and maintaining regulatory documentation, international product registrations, certificates, technical files, and global label compliance.
University of ColoradoRegulatory Affairs Coordinator (Open Rank: Intermediate - Senior) University of ColoradoRegulatory Affairs Coordinator (Open Rank: Intermediate - Senior)Denver, CO$52,860–$67,239 / yearPrimary duties will include, but not be limited to: submissions to the Institutional Review Board (IRB) of record including amendments, unanticipated problems, continuing reviews, and study closures; maintenance of the investigator site file/regulatory binder and all essential documents including documentation of appropriate training and delegation for all personnel; submissions to internal University and Hospital research portals; acting as primary regulatory contact person for sponsors/Contract Research Organizations (CROs)/coordinating centers; and training UCD Neurology Clinic Research personnel to promote good clinical practice (GCP) and compliance with all applicable regulations. Create/organize regulatory binder and/or electronic files for new studies and maintain regulatory binder and/or electronic files throughout the course of the study, file/update all required documents and ongoing training/certifications appropriately.
University of Colorado Anschutz Medical CampusNewRegulatory Affairs Coordinator (Open Rank: Intermediate - Senior) University of Colorado Anschutz Medical CampusRegulatory Affairs Coordinator (Open Rank: Intermediate - Senior)Aurora, CO$52,860–$67,239 / yearPrimary duties will include, but not be limited to: submissions to the Institutional Review Board (IRB) of record including amendments, unanticipated problems, continuing reviews, and study closures; maintenance of the investigator site file/regulatory binder and all essential documents including documentation of appropriate training and delegation for all personnel; submissions to internal University and Hospital research portals; acting as primary regulatory contact person for sponsors/Contract Research Organizations (CROs)/coordinating centers; and training UCD Neurology Clinic Research personnel to promote good clinical practice (GCP) and compliance with all applicable regulations. Application Materials Required: Cover Letter, Resume/CV, List of References Job Category: Research Services Primary Location: Hybrid Department: U0001 -- Anschutz Med Campus or Denver - 20244 - SOM-NEUR GENERAL OPERATIONS Schedule: Full-time Posting Date: Jun 5, 2026 Unposting Date: Ongoing Posting Contact Name: Neurology-hr Posting Contact Email: Neurology-hr@cuanschutz.edu Position Number: 00841737
Scout Clean EnergyManager, Government and Regulatory Affairs - PJM and MISO Scout Clean EnergyManager, Government and Regulatory Affairs - PJM and MISOBoulder, CO$110,000–$150,000Understanding of state legislative processes and utility commission regulations unique to renewable energy technologies and across multiple disciplines including demand drivers, transmission, interconnection, finance, tax, origination, siting, permitting and land use. This individual will join a small team reporting to the Director, Government and Regulatory Affairs, and will coordinate closely with internal and external subject matter experts to advance Scout’s policy strategy and support execution across the development and operating portfolio.
Artech LLCNewDirector, Regulatory Affairs - Compliance Systems and Labeling Artech LLCDirector, Regulatory Affairs - Compliance Systems and LabelingLakewood, CO$196,500–$245,600 / yearTarget Pay Range: $196,500.00 to $245,600.00 - Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data. Collaborate with senior teams to define strategy and compliance programs, playing an integral role in launching new products and supporting established lines.
The University of Colorado SystemNewRegulatory Affairs Coordinator (Open Rank: Intermediate - Senior) The University of Colorado SystemRegulatory Affairs Coordinator (Open Rank: Intermediate - Senior)Denver, CO$52,860–$67,239 / yearKey responsibilities include facilitating completion of initial essential regulatory documents (FDA 1572, Financial Disclosure forms, PI signature pages, etc), creating/organizing regulatory binder and/or electronic files for new studies and maintaining regulatory binder and/or electronic files throughout the course of the study, filing/updating all required documents and ongoing training/certifications appropriately, overseeing training logs and delegation of duties logs, working with study coordinator to ensure completion prior to enrollment and ongoing accurate maintenance throughout the study, maintaining documentation of all relevant training, preparing for and managing regulatory portion of industry study monitor visits, addressing all regulatory action items, creating informed consent documents for new studies and updating informed consent documents as needed throughout the study, facilitating process for investigator receipt and evaluation of external IND safety reports, and other duties as assigned. Qualifications: minimum qualifications: entry level: a bachelor's degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, or a directly related field from an accredited institution, intermediate level: a bachelor's degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, or a directly related field from an accredited institution 1 year professional experience in a clinical research setting with regulatory responsibilities, senior level: a bachelor's degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, or a directly related field from an accredited institution 2 years professional experience in a clinical research setting with regulatory responsibilities.
University of ColoradoOpen Rank Regulatory Affairs Coordinator (RAC) (Entry - Senior) University of ColoradoOpen Rank Regulatory Affairs Coordinator (RAC) (Entry - Senior)Denver, CO$52,860–$70,833 / yearThe Regulatory Affairs Coordinator (RAC) will work closely with the HCTU Leadership Team, Principal Investigators, Industry Sponsor/CRO Representatives, IRBs, and other departments on campus to provide support for the Division's clinical trial portfolio. Why Join Us: Investigators in the Division of Hematology's Blood Cancer Program are actively engaged in multiple research activities aimed at improving outcomes for patients with blood cancers and related disorders.
MRINetwork JobsDirector of Quality and Regulatory Affairs MRINetwork JobsDirector of Quality and Regulatory AffairsDenver, ColoradoDirect experience in and knowledge of business and management principles involved in tactical execution, strategic planning, resource allocation, human resources modeling, leadership techniques, production methods, and coordination of people and resources. As Director of Regulatory Affairs – Compliance Systems and Labeling, you’ll direct regulatory and labeling activities and collaborate with senior teams to define strategy and compliance programs.
System OneDirector, Regulatory Affairs (Medical Devices) System OneDirector, Regulatory Affairs (Medical Devices)Denver, Colorado$195,000–$245,000 / yearA well-established and growth-oriented medical device organization is seeking a strategic regulatory leader to guide global regulatory affairs and labeling strategy across a diverse product portfolio. Required Experience:10+ years of progressive regulatory affairs experience within medical devices (combination product experience strongly preferred).
Medtronic PlcPrin Regulatory Strategy Spec Medtronic PlcPrin Regulatory Strategy SpecLafayette, COIf you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: 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, and Simple Steps (global well-being program).
Rowan Digital InfrastructureRegulatory Affairs & Public Policy, Senior Associate Rowan Digital InfrastructureRegulatory Affairs & Public Policy, Senior AssociateDenver, ColoradoThis role serves as a core analytical and operational resource, enabling the team to monitor, assess, and respond to legislative and regulatory developments that impact project siting, energy procurement, and overall business strategy. This role will help support bill tracking, regulatory dockets, and internal policy workflows, while producing clear, decision ready analysis for cross functional stakeholders.
University of ColoradoRegulatory Affairs Coordinator (RAC) (Open Rank, Entry to Senior) University of ColoradoRegulatory Affairs Coordinator (RAC) (Open Rank, Entry to Senior)Aurora, CO$50,996–$64,867 / yearApplication Materials Required: Cover Letter, Resume/CV, List of References : Research Services : Hybrid Department: U0001 -- Anschutz Med Campus or Denver - 20164 - SOM-MED-BoneMarrow Transplant : Full-time : Jan 9, 2026 : Ongoing Posting Contact Name: Dan Page Posting Contact Email: daniel.page@cuanschutz.edu (https://apptrkr.com/get_redirect.php?id=6848194&targetURL=daniel.page@cuanschutz.edu) In addition, if you work in certain research areas or perform certain safety sensitive job duties, you must enroll in the occupational health medical surveillance program (https://apptrkr.com/get_redirect.php?id=6848194&targetURL=https://research.cuanschutz.edu/ehs/home/divisions/occupational-health/oh-enrollment) .
CleerlyVice President, Regulatory Strategy and Innovation CleerlyVice President, Regulatory Strategy and InnovationDenver, CO$280,000–$300,000 / yearCandidates located in higher-cost labor markets, including California, Washington, New York, New Jersey, Connecticut, Massachusetts, and Washington, DC represent the middle to high end of the range, while candidates located in all other U.S. locations represent the low to middle end of the range. Portfolio Architecture: Architect regulatory strategies enabling independent iteration of AI algorithms distinct from core platforms, defining regulatory logic for modular systems (AI engines, reporting engines, workflow tools).
Highridge IncRegulatory Associate Highridge IncRegulatory AssociateWestminster, COYou will have the opportunity to attend surgical labs, engage with project teams, learn about regulatory affairs, hone your writing skills, and immerse yourself in a medical device organization committed to its customers. As an RA team member, you will work closely with the rest of the RA team to ensure distribution of product within regulatory guidelines, and work with international team members to facilitate international submissions.
Financial Industry Regulatory Authority IncProgram Manager, Regulatory Operations Financial Industry Regulatory Authority IncProgram Manager, Regulatory OperationsDenver, COFINRA employees are required to disclose to FINRA all brokerage accounts that they maintain, and those in which they control trading or have a financial interest (including any trust account of which they are a trustee or beneficiary and all accounts of a spouse, domestic partner or minor child who lives with the employee) and to authorize their broker-dealers to provide FINRA with duplicate statements for all of those accounts. Additional insurance includes basic life, accidental death and dismemberment, supplemental life, spouse/domestic partner and dependent life, and spouse/domestic partner and dependent accidental death and dismemberment, short- and long-term disability, long-term care, business travel accident, disability and legal.
Black & Veatch Holding CoConsultant, Rates & Regulatory Black & Veatch Holding CoConsultant, Rates & RegulatoryDenver, CO$103,147–$172,271 / yearRecognized by Glassdoor as a 2023 Top 100 place to work and winner of the Newsweek's 2023 America's Greatest Workplaces for Diversity, Black & Veatch allows you to lend your talent and perspective to humanity's biggest challenges in a flexible environment where you are empowered to grow and explore new possibilities. Black & Veatch's Infrastructure Advisory Business provides a portfolio of solutions focused on the asset lifecycle, including Asset Management & Operations & Maintenance, Infrastructure Technology, Cybersecurity Solutions, Planning, and Transactions.
Black & VeatchNewConsultant, Rates & Regulatory Job Details | Black & Veatch Family of Companies Black & VeatchConsultant, Rates & Regulatory Job Details | Black & Veatch Family of CompaniesDenver, CO$103,147–$172,271 / yearRecognized by Glassdoor as a 2023 Top 100 place to work and winner of the Newsweek's 2023 America's Greatest Workplaces for Diversity , Black & Veatch allows you to lend your talent and perspective to humanity's biggest challenges in a flexible environment where you are empowered to grow and explore new possibilities. Black & Veatch's Infrastructure Advisory Business provides a portfolio of solutions focused on the asset lifecycle, including Asset Management & Operations & Maintenance, Infrastructure Technology, Cybersecurity Solutions, Planning, and Transactions.
GHD Group Pty LtdRegulatory SME (MI) GHD Group Pty LtdRegulatory SME (MI)GOLDEN, COGHD will reimburse 50% of the cost of the following to maximum of $250.00 reimbursement annually for such items as: Health club membership fees, Home exercise equipment purchases, Bicycles, Race, run & marathon entrance fees, Smoking cessation programs, Weight loss programs (i.e. Weight Watchers, Jenny Craig), Fitbits and Fitness Tracking devices. The role supports project delivery, business development, and regulatory risk management across exploration, drilling, production, and remediation activities.
Danaher CorpPrincipal, RA Specialist Danaher CorpPrincipal, RA SpecialistBoulder, CORemote$110,000–$135,000 / yearIn this role, you will have the opportunity to: Author and lead the creation of regulatory documents (regulatory submissions/filings, registration and listing, technical files, etc.) to obtain global approvals to commercially distribute products; collaborates with international colleagues in global regions to submit application/registration documents. Provide guidance and approve regulatory/quality documentation related to new product development deliverables acting as core team member conducting regulatory assessments related to design changes, advising and approving protocols, reports, marketing material, etc.
HistoSonics IncSenior Procedure Development Specialist HistoSonics IncSenior Procedure Development SpecialistCORemoteWork closely with the HistoSonics Education, Marketing, Sales and R&D teams to deliver world-class customer and employee training and education programs that enhance the value of the organization. HistoSonics is a medical device company, founded in 2009, that has developed a non-invasive, sonic beam therapy platform that uses histotripsy, which is capable of destroying targeted liver tumors.
University of ColoradoPre-Award Specialist (Open-Rank) University of ColoradoPre-Award Specialist (Open-Rank)Boulder, CO$50,160–$63,804 / yearThere is a lot of training up front as this position must learn a Medicare Coverage Analysis (MCA), oncology clinical trial protocols, processes and procedures of the oncology clinical trial Post Award specialist, the oncology clinical trial finance/billing specialist, clinic staff. Job Summary: The Oncology Clinical Research Pre Award Specialist is responsible for developing, negotiating, finalizing and reviewing budgets for clinical trials conducted by faculty members of the University of Colorado Cancer Center at University of Colorado Hospital (UCH).
U.S. Department of Veterans AffairsProgram Specialist U.S. Department of Veterans AffairsProgram SpecialistGolden, CO$68,819–$108,251 / year2) knowledge applying Federal, State laws, rules, and regulations relative to compliance and the conduct of investigative studies, (3) interpreting and analyzing data using discretion to implement a wide range of research policies and procedures, (4) preparing and conducting study presentations, trainings, and briefings (5) reviewing and preparing trial budget, and (6) assisting in developing action plans to resolve problems or improve efficiency, and implementation of new methods. (2) interpreting Federal, State laws, rules, and regulations relative to compliance and the conduct of investigative studies, (3) applying analytical and evaluative principles to resolve issues and accomplish program goals for a clinical, medical, and/or research department/organization, (4) creating, maintaining, and disseminating electronic information and documents/files; effectively communicates, orally and in writing, between agencies and across organizational levels to coordinate research needs and deliver requested information.
Google LLCWorkforce Data Security Specialist Google LLCWorkforce Data Security SpecialistBoulder, CONote: By applying to this position you will have an opportunity to share your preferred working location from the following: Chicago, IL, USA; Ann Arbor, MI, USA; Atlanta, GA, USA; Austin, TX, USA; Boulder, CO, USA; Los Angeles, CA, USA; Seattle, WA, USA; Washington D.C., DC, USA. Whether recruiting the next Googler, refining our core programs, developing talent, or simply looking for ways to inject some more fun into the lives of our Googlers, we bring a data-driven approach that is reinventing the human resources field.
U.S. Department of Veterans AffairsNewIT Specialist U.S. Department of Veterans AffairsIT SpecialistDenver, CO$89,508–$116,362 / yearCustomer Service - Works with clients and customers (that is, any individuals who use or receive the services or products that your work unit produces, including the general public, individuals who work in the agency, other agencies, or organizations outside the Government) to assess their needs, provide information or assistance, resolve their problems, or satisfy their expectations; knows about available products and services; is committed to providing quality products and services. The Department of Veterans Affairs performs pre-employment reference checks as an assessment method used in the hiring process to verify information provided by a candidate (e.g., on resume or during interview or hiring process); gain additional knowledge regarding a candidates abilities; and assist a hiring manager with making a final selection for a position.
U.S. Department of Veterans AffairsIT Specialist (SYSANALYSIS) U.S. Department of Veterans AffairsIT Specialist (SYSANALYSIS)Denver, CO$106,437–$138,370 / yearCustomer Service - Works with clients and customers (that is, any individuals who use or receive the services or products that your work unit produces, including the general public, individuals who work in the agency, other agencies, or organizations outside the Government) to assess their needs, provide information or assistance, resolve their problems, or satisfy their expectations; knows about available products and services; is committed to providing quality products and services. Specialized experience is defined as: Experience in the planning, testing and implementation of Directory Services infrastructure technologies in a large multi-domain Active Directory (AD) Environment, including AD object management, user and group management, Group Policy management, support of Domain Name System (DNS) services and user access and authentication.
State of ColoradoCPRG Methane Grant Support Specialist - EPS I State of ColoradoCPRG Methane Grant Support Specialist - EPS IDenver, CO$65,736–$97,104 / yearAs part of this commitment, our agency will assist individuals who have a disability with any reasonable accommodation requests related to employment, including completing the application process, interviewing, completing any pre-employment testing, participating in the employee selection process, and/or to perform essential job functions where the requested accommodation does not impose an undue hardship. The Work Unit: The Policy Innovations Unit within the Office of Innovations in Planning and Air Quality Data develops innovative strategies to achieve long-term air pollution goals, including ozone attainment and the state's greenhouse gas reduction targets.
EverDrivenInsurance, Legal, and Policy Specialist EverDrivenInsurance, Legal, and Policy SpecialistGreenwood Village, COThis role will report to EverDriven's Chief Policy and Legal Officer in supporting Legal and Policy initiatives, and will partner closely with Contract Management, Operations, Legal, and Finance to ensure insurance coverage aligns with contractual and business requirements, and to drive a culture of risk awareness across the organization. EverDriven is the nation's leading provider of alternative student transportation, partnering with school districts to serve students who need it most—including those experiencing homelessness, living with disabilities, or outside traditional bus routes.
U.S. Department of Veterans AffairsNewRecords and Information Management Specialist U.S. Department of Veterans AffairsRecords and Information Management SpecialistLakewood, CO$99,800–$129,742 / yearSpecialized experience is defined as work that involves, but is not limited to, development and maintenance of records management and privacy programs and/or initiatives, conducting studies to determine program needs, ensuring the protection of Veteran, employee and other agency sensitive information from unauthorized use, disposal and destruction. MINIMUM QUALIFICATION REQUIREMENT: You may qualify based on your experience and/or education as described below: GS-12 Grade Level: Specialized Experience: To qualify for the Records and Information Management Specialist, GS-0308-12 position, you must have at least one (1) year of specialized experience equivalent to at least the next lower grade level (GS-11) in the Federal service obtained in either the public or private sectors.
Primoris Services CorporationHSE Specialist - Communications Primoris Services CorporationHSE Specialist - CommunicationsDenver, Colorado$80,000Position OverviewWe are seeking a highly motivated Entry-Level HSE Specialist to provide front-line HSE support across an assigned operating region. The ideal candidate will be passionate about workplace safety and environmental responsibility, with strong communication skills to effectively convey HSE policies and procedures to diverse teams.
Links Technology Solutions, Inc.Logistics Specialist III Links Technology Solutions, Inc.Logistics Specialist IIIParker, COOur Aerospace client is seeking a detail-oriented Logistics Specialist II to support the coordination, documentation, and execution of logistics operations for critical materials, equipment, and systems. This role plays a key part in ensuring the accurate tracking, storage, and shipment of spares, tools, test equipment, and associated documentation within a regulated environment.
Medtronic PlcPrincipal Customer Marketing Specialist - Capnography, Acute Care and Monitoring Medtronic PlcPrincipal Customer Marketing Specialist - Capnography, Acute Care and MonitoringLafayette, CORemoteThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: 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, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. (Medtronic) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.