Clinical Research and Regulatory Affairs Specialist University of ColoradoClinical Research and Regulatory Affairs SpecialistDenver, CO$71,517–$95,833 / yearJob Summary: The Gates Institute at the University of Colorado Anschutz seeks a highly motivated, detail-oriented Clinical Research and Regulatory Affairs Specialist to support the product and clinical safety lifecycle starting at the preclinical development stage through first-in-human (FIH) Phase I clinical trials through safety monitoring & risk assessment, regulatory compliance & documentation, data integrity & quality control, and process optimization. Key Responsibilities: Regulatory Operations: Coordinate regulatory activities supporting investigator-initiated cell and gene therapy (CGT) programs from preclinical development through first-in-human (FIH) Phase I clinical trials, including preparation and submission of IND applications, protocol amendments, annual reports, and other regulatory documentation.
Sr 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).
Director, Regulatory Affairs 3D Systems CorpDirector, Regulatory AffairsLittleton, CO$177,000–$266,000 / yearUSA-CO-Littleton'','''','''','''',''80127'',''Manager with Direct Reports'',''Manager with Direct Reports'',''Yes, 25 % of the Time'',''Yes, 25 % of the Time'',''Employee'',''Employee'',''Jun 29, 2026, 9:30:20 AM'',''Jun 29, 2026, 9:30:20 AM'',''false'',''170351'',''170351'',''true'',''170351'',''false'',''Submission for the position: Director, Regulatory Affairs - (Job Number: 26000055)'',''false'',''170351'',''false'',''true''. In this position, you will lead the development and execution of global regulatory strategies for a diverse portfolio of patient-specific and additively manufactured medical devices, including implantable solutions, digitally enabled surgical planning technologies, and advanced manufacturing platforms.
Prin Regulatory Affairs Spec - Core Surgical innovations MedtronicPrin Regulatory Affairs Spec - Core Surgical innovationsLafayette, ColoradoResponsibilities include participating on product development teams, developing global regulatory strategies, preparing US and international regulatory submissions, supporting pre and post market regulatory compliance activities and evaluating proposed product changes for regulatory impact and preparing necessary documentation. 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.
Prin Regulatory Affairs Spec - Core Surgical innovations Medtronic PlcPrin Regulatory Affairs Spec - Core Surgical innovationsLafayette, COResponsibilities include participating on product development teams, developing global regulatory strategies, preparing US and international regulatory submissions, supporting pre and post market regulatory compliance activities and evaluating proposed product changes for regulatory impact and preparing necessary documentation. 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.
Associate or Senior Associate, Regulatory Affairs Invenergy LLCAssociate or Senior Associate, Regulatory AffairsDenver, CO$93,000–$113,000 / yearThey will support the regulatory team in representing Invenergy before state and federal economic regulators, transmission service providers, regional transmission organizations/independent system operators, and state and regional trade associations on behalf of Invenergy's operating assets as well as its pipeline of development projects. Collaborate with Regulatory Affairs team members in the Western region, ERCOT, and across regions, as well as other internal departments such as development, asset management, legal, transmission, interconnection and origination functions.
Associate, Regulatory Affairs InvenergyAssociate, Regulatory AffairsDenver, ColoradoThey will support the regulatory team in representing Invenergy before state and federal economic regulators, transmission service providers, regional transmission organizations/independent system operators, and state and regional trade associations on behalf of Invenergy's operating assets as well as its pipeline of development projects. Collaborate with Regulatory Affairs team members in the Western region, ERCOT, and across regions, as well as other internal departments such as development, asset management, legal, transmission, interconnection and origination functions.
Manager, Government and Regulatory Affairs - SPP and ERCOT Scout Clean Energy LLCManager, Government and Regulatory Affairs - SPP and ERCOTBoulder, COPrimary coverage includes active participation in ERCOT and SPP stakeholder processes and related proceedings, with additional engagement across states where Scout operates and develops projects (currently including Texas, South Dakota, Oklahoma, Missouri, and North Dakota; coverage may evolve). Scout Clean Energy is seeking a motivated and collaborative Manager, Government and Regulatory Affairs to help manage regulatory and market risk by protecting and enhancing the value of Scout's operating assets across the SPP and ERCOT footprints.
Manager, Regulatory Affairs - West Invenergy LLCManager, Regulatory Affairs - WestDenver, CO$129,000–$155,000 / yearThe Manager, Regulatory Affairs will represent Invenergy before and manage relationships with state economic and environmental regulators, transmission system operators, and regional trade associations in the West on behalf of Invenergy's existing assets as well as its pipeline of development projects. Build personal relationships with external stakeholders managing regulatory issues, including those with leadership positions at entities like public utility commissions, regional transmission entities (CAISO), regional trade organizations, and other relevant stakeholders.
Manager, Regulatory Affairs - West InvenergyManager, Regulatory Affairs - WestDenver, ColoradoThe Manager, Regulatory Affairs will represent Invenergy before and manage relationships with state economic and environmental regulators, transmission system operators, and regional trade associations in the West on behalf of Invenergy's existing assets as well as its pipeline of development projects. Build personal relationships with external stakeholders managing regulatory issues, including those with leadership positions at entities like public utility commissions, regional transmission entities (CAISO), regional trade organizations, and other relevant stakeholders.
Director 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.
Regulatory Affairs Specialist Medtronic PlcRegulatory Affairs SpecialistLafayette, 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).
Sr Regulatory Affairs Manager Medtronic PlcSr Regulatory Affairs ManagerLafayette, 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). As a member of the RA leadership team, this role collaborates closely with the network of RA leaders along with cross-functional team members across the operating unit to ensure RA is equipped with the tools, processes, and systems needed to execute effectively throughout the full product lifecycle.
Manager, Government and Regulatory Affairs - SPP and ERCOT Scout Clean EnergyManager, Government and Regulatory Affairs - SPP and ERCOTBoulder, CO$110,000–$150,000 / yearPrimary coverage includes active participation in ERCOT and SPP stakeholder processes and related proceedings, with additional engagement across states where Scout operates and develops projects (currently including Texas, South Dakota, Oklahoma, Missouri, and North Dakota; coverage may evolve). Because Scout’s portfolio in this region is weighted toward operating projects, the role will focus on issues that affect day-to-day operations and commercial outcomes and will help craft and advocate for rules that are stable, effective, and aligned with renewable resources’ technical capabilities.
Sr Manager, Regulatory Affairs Zimmer Biomet Holdings IncSr Manager, Regulatory AffairsEnglewood, CO$120,000–$150,000 / yearBacked by the global scale of Zimmer Biomet, you will champion both high-stakes new product introductions and critical market maintenance, ensuring our life-changing medical devices reach patients without delay. Paragon 28, a premier Zimmer Biomet company, is seeking an ambitious Senior Manager of Regulatory Affairs, Domestic, to spearhead our United States regulatory footprint.
Manager, Government And Regulatory Affairs - SPP And Ercot Scout Clean EnergyManager, Government And Regulatory Affairs - SPP And ErcotBoulder, COPrimary coverage includes active participation in ERCOT and SPP stakeholder processes and related proceedings, with additional engagement across states where Scout operates and develops projects (currently including Texas, South Dakota, Oklahoma, Missouri, and North Dakota; coverage may evolve). Because Scout's portfolio in this region is weighted toward operating projects, the role will focus on issues that affect day-to-day operations and commercial outcomes and will help craft and advocate for rules that are stable, effective, and aligned with renewable resources' technical capabilities.
NewRegulatory Affairs Coordinator Rocky Mountain Cancer CentersRegulatory Affairs CoordinatorDenver, Colorado$65,000–$95,000 / yearRocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Regulatory Affairs Coordinator in Denver. -Facilitates collection of site training documents from study initiation visits as well as coordinates and collects ongoing amendment training documents.
Open 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.
Director, 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).
Senior Manager, Regulatory Affairs CONMED CorporationSenior Manager, Regulatory AffairsDenver, Colorado$138,700–$215,100 / yearMinimum 8 years of directly relevant Regulatory Affairs experience in the medical device industry, including hands-on authorship, review, or leadership of regulatory submissions such as 510(k)s, Technical Documentation/Technical Files, pre-submissions, international registrations, or related applications. Partners with senior business, R&D, Clinical, Quality, Marketing, and Operations leaders to anticipate regulatory risks, influence product and portfolio decisions, and build a high-performing regulatory affairs team aligned to business objectives and applicable global requirements.