7,676 regulatory operations jobs at 3,589 companies in United States
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Regulatory Operations Lead
United States
$160k-$200k/yrRemoteFull Time
AirbnbNASDAQ: ABNB: Online marketplace for vacation rentals and travel experiences.
10+ YOE10+ years in regulatory operations, legal/policy compliance, consulting, project management, or related fields; ability to navigate ambiguity and lead multiple projects; experience building scalable technical solutions and processes; strong communication and stakeholder management.
7+ YOEBachelor's in life sciences or pharmacy required; 7+ years in regulatory operations, program/project management, or business operations in biopharma; strong leadership, stakeholder management, and Microsoft Office skills.
Microsoft PowerPoint, Microsoft Excel, Microsoft Word, Microsoft Teams, SharePoint, Planisware, Veeva RIM, Veeva
Morgan StanleyNYSE: MS: Global financial services firm providing investment and wealth management.
4+ YOEExperience with regulatory transaction reporting (CAT/CFTC), strong control and risk focus, 4+ years relevant experience, knowledge of trade lifecycle, project/change management, excellent communication.
Pacira BioSciencesNASDAQ: PCRX: Develops non-opioid pain management and regenerative health products.
8+ YOEBachelor's in life sciences, 8+ years in regulatory operations (pharma/biotech), Veeva RIM SME, global submission planning/tracking, MS Word/Excel/PowerPoint, project management tools, training and process improvement experience.
Veeva RIM, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project, Smartsheet
Operations Regulatory Specialist II (Hybrid location)
Dayton or United States
$63k-$100k/yrHybridFull Time
CareSource: Provides public health insurance plans and care management services.
2+ YOEBachelor's or equivalent experience, 2+ years healthcare operations experience, regulatory/compliance knowledge preferred, advanced Microsoft Word/Excel/PowerPoint, data analysis, claims and coding knowledge (CPT, ICD-9/10, HCPCS), strong communication and writing skills.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, CPT, ICD-9, ICD-10, HCPCS
Merida Biosciences: Developing precision therapeutics for autoimmune and allergic diseases.
7+ YOEBachelors in life sciences required; 7+ years regulatory affairs/operations experience in pharma/biotech; experience with RIMS/EDMS/Veeva Vault, eCTD, project planning tools and Microsoft Office; knowledge of FDA/EMA/ICH standards.
RIMS, EDMS, Veeva Vault Regulatory, eCTD, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams, Smartsheet, Microsoft Project
Acadia PharmaceuticalsNASDAQ: ACAD: Develops and sells medicines for neurological and rare diseases.
12+ YOE8+ Mgmt12+ years in Regulatory Operations/Regulatory Affairs; 8+ years leadership; experience with regulatory systems and submissions; Veeva Vault RIM and eCTD tools; travel; Bachelor's in life sciences.
Veeva Vault RIM, eCTD tools, regulatory information management, publishing platforms
Platinum Dermatology Partners: Provides management support and clinical services to dermatology practices.
5+ YOEBachelor's degree and 5+ years regulatory operations or healthcare compliance experience; experience with clinic permits and CLIA inspections; strong organizational, communication, and project management skills; ability to travel.
The START Center for Cancer Research: Global network of early-phase oncology clinical trial sites.
5+ YOEHigh school diploma, 5 years regulatory research experience, proficiency with Microsoft Outlook 365 and regulatory document systems (Veeva, Advarra E-Reg), strong clinical research terminology and organizational skills.
Balt: Manufacturer of medical devices for treating neurovascular diseases
1.5+ YOEBA/BS in scientific/technical field,1.5+ years in regulated industry,experience with regulatory documentation,MS Office and Adobe Acrobat skills,ability to manage regulatory systems and coordinate cross-functional partners.
Microsoft Office, Adobe Acrobat, Product Lifecycle Management Systems
Nurix TherapeuticsNASDAQ: NRIX: Develops targeted protein degradation medicines for cancer and inflammation.
5+ YOEBachelor's in life sciences, 5+ years in regulatory affairs/operations, proficient with Veeva RIMS SCP and publishing tools (DocuBridge, GlobalSubmit, VeevaVault Submission), knowledge of 21 CFR/ICH/GCP/GMP/eCTD, MS Word/Excel/PowerPoint/Smartsheet.
Veeva RIMS SCP, Veeva RIMS, VeevaVault Submission, DocuBridge, GlobalSubmit, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Smartsheet
Publicis GroupeEuronext Paris: PUB: Global advertising and digital transformation agency holding.
2+ YOEBachelor's degree and 2+ years preparing complex regulatory/promotional submission deliverables; strong Adobe Acrobat and Microsoft Office skills; excellent communication, organization, and technical writing.
Adobe Acrobat, Microsoft Office Suite, Adobe InDesign, Adobe Photoshop
ExelixisNASDAQ: EXEL: Discovers and commercializes innovative medicines for cancer treatment.
5+ YOEDeep knowledge of global regulatory submission requirements, experience planning and managing electronic submissions, Veeva RIM experience, strong communication and cross-functional collaboration skills; travel ~20%.
IncyteNasdaq: INCY: Develops and manufactures innovative oncology and inflammation medicines.
Bachelor's degree or equivalent experience; experience in regulatory affairs with eCTD, electronic publishing, RIM/EDMS and submissions to global health authorities; strong document management, writing, and organizational skills.
eCTD, SPL, RIM, EDMS, Microsoft Word, Adobe, Adobe plug-ins
Supervisor, Credentialing and Regulatory Operations
Boston or Bethlehem or New York or Holmdel
$83k-$136k/yrHybridFull Time
Guardian Life: Provides life, disability, dental, and vision insurance products.
Proven credentialing and people leadership experience in regulated healthcare/insurance; subject-matter expertise in dental provider credentialing and regulatory requirements; experience with process improvement and automation.
Hilcorp Energy: Explores and produces oil and natural gas in mature fields.
1+ YOE1+ year oil and gas operations tech experience, strong data management, administrative and communication skills, proficiency with Microsoft Office; high school diploma or GED required.
Microsoft Excel, Microsoft Word, Microsoft Outlook, Microsoft Teams, SAP, Siteview/Wellview, PowerBI
Novotech: Global clinical research services for biotech drug development.
5+ YOEGraduate in clinical/pharmacy/life sciences, 5+ years CRO/biotech/pharma experience in trial start-up or regulatory operations, strong knowledge of regulations, matrix working, presentation and documentation skills, high English proficiency.
CencoraNYSE: COR: Distributes pharmaceuticals and provides global healthcare supply chain solutions.
2+ YOEHigh school diploma, 2+ years compliance/regulatory or distribution experience, knowledge of federal/state regulatory agencies and regulations, Microsoft Word/Excel/PowerPoint skills, strong written and verbal communication, audit and inspection experience.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
Director / Senior Director of Regulatory Operations
San Diego, California, United States
$205k-$268k/yrHybridFull Time
Artiva BiotherapeuticsNASDAQ: ARTV: Develops allogeneic natural killer cell-based therapies for various diseases.
15+ YOE5+ Mgmt15+ years regulatory affairs/operations experience with 5+ years leadership; deep eCTD and Veeva Vault RIM expertise; proven end-to-end global submission delivery; SOPs and RIM ownership.