Analyst, Regulatory Affairs Oscar HealthAnalyst, Regulatory AffairsDallas, TXRemote$28.30–$37.15 / hourYou will support the Regulatory Affairs Evidence of Coverage team by serving as a resource on Oscar processes and identify risks to escalate in partnership with their manager. Responsibilities: Support annual QHP filings by ensuring the quality and timeliness of annual filing inputs through initial submission and regulator facing negotiation periods.
Analyst, Regulatory Affairs Oscar Health IncAnalyst, Regulatory AffairsDallas, TXRemote$28.30–$37.15 / hourYou will support the Regulatory Affairs Evidence of Coverage team by serving as a resource on Oscar processes and identify risks to escalate in partnership with their manager. Responsibilities: Support annual QHP filings by ensuring the quality and timeliness of annual filing inputs through initial submission and regulator facing negotiation periods.
Regulatory Affairs Associate ARKRAY USA IncRegulatory Affairs AssociatePlano, TXSupport quality system activities as assigned, including audit support, validation/change control support, supplier activities, internal audit participation, and QMS compliance activities (FDA QMSR, ISO 13485, OSHA). Support product launch regulatory work such as Regulatory Master Plans, labeling program coordination, UDI/GUDID activities, facility registrations/device listings, import inspections/holds, and related documentation support.
Sr. Regulatory Affairs Manager Karwell TechnologiesSr. Regulatory Affairs ManagerDallas, TXAssists in preparing and organizing all necessary documentation required for regulatory inspections and inspection readiness initiatives ensuring completeness, accuracy, and accessibility of records related to QOL initiatives. Support coordination with global regulatory counterparts to ensure alignment of regional regulatory strategies and submissions with global development plans and corporate objectives.
Sr. Regulatory Affairs Manager Katalyst Healthcares & Life SciencesSr. Regulatory Affairs ManagerDallas, TXAssists in preparing and organizing all necessary documentation required for regulatory inspections and inspection readiness initiatives ensuring completeness, accuracy, and accessibility of records related to QOL initiatives. Support coordination with global regulatory counterparts to ensure alignment of regional regulatory strategies and submissions with global development plans and corporate objectives.
NewDirector, Regulatory Affairs Argon Medical Devices IncDirector, Regulatory AffairsPlano, TexasFull timeActively communicate and collaborate with internal and external partners and across functions including Marketing, Commercial Regional Leaders, Engineering, R&D, Site Quality, Operations to support new product development and global registration strategy. This key leadership role involves developing and implementing regulatory strategies, mentoring teams and managing critical interactions with regulatory agencies across the globe.
Regulatory Affairs Manager Karwell TechnologiesRegulatory Affairs ManagerDallas, TXMust be able to work effectively in a strongly matrixed team-oriented structure using excellent communication, interpersonal and relationship management skills to successfully interact with Clinical, Research and Development, Manufacturing, Quality, Marketing, Operations and corporate partner counterparts on complex projects. Demonstrated hands-on experience in preparing regulatory clearance/approvals for IVD products in the EU, USA, OUS; (Preferred experience: working experience with IVD submissions under IVDR Regulations is highly desirable).
Regulatory Affairs Manager Katalyst Healthcares & Life SciencesRegulatory Affairs ManagerDallas, TXMust be able to work effectively in a strongly matrixed team-oriented structure using excellent communication, interpersonal and relationship management skills to successfully interact with Clinical, Research and Development, Manufacturing, Quality, Marketing, Operations and corporate partner counterparts on complex projects. Demonstrated hands-on experience in preparing regulatory clearance/approvals for IVD products in the EU, USA, OUS; (Preferred experience: working experience with IVD submissions under IVDR Regulations is highly desirable).
Regulatory Affairs Coordinator, Three locations: ( Portage MI, San Jose, Flower Mound Texas) Matlen Silver, Inc.Regulatory Affairs Coordinator, Three locations: ( Portage MI, San Jose, Flower Mound Texas)Flower Mound, TXJob overview: The Product Environmental Compliance Coordinator (Contractor) supports the Endoscopy Divisions Product Environmental Compliance program by helping ensure products meet global environmental regulations such as RoHS, REACH, POPs, WEEE, and California Proposition 65. This individual contributor role focuses on maintaining accurate compliance data, coordinating supplier outreach, supporting time-sensitive projects, and preparing reports that track progress and support decision-making.
Coordinator, Regulatory Affairs - Onsite Roth Staffing CompaniesCoordinator, Regulatory Affairs - OnsiteFlower Mound, Texas$34.14 / hourKey responsibilities include extracting and reconciling data from multiple systems, managing submissions to third-party compliance evidence providers, researching and responding to customer or sales-related compliance inquiries, revising compliance documentation, and supporting non-conformance investigations and corrective actions. The Product Environmental Compliance Coordinator (Contractor) supports the Endoscopy Division's Product Environmental Compliance program by helping ensure products meet global environmental regulations such as RoHS, REACH, POPs, WEEE, and California Proposition 65.
Senior Regulatory Affairs Analyst Keurig Dr Pepper IncSenior Regulatory Affairs AnalystFrisco, TX$76,400–$115,000 / yearThe analyst also monitors and interprets relevant government and technical information impacting our brands, develops finished-product regulatory specifications, and provides regulatory guidance to business partners and cross-functional project teams. By enabling compliant, science-based claims, labeling, and advertising, the function protects consumers and the business while supporting KDPs competitive edge.
Coordinator, Regulatory Affairs - Skilled Apidel TechnologiesCoordinator, Regulatory Affairs - SkilledFlower Mound, TXContractorKey responsibilities include extracting and reconciling data from multiple systems, managing submissions to third-party compliance evidence providers, researching and responding to customer or sales-related compliance inquiries, revising compliance documentation, and supporting non-conformance investigations and corrective actions. The Product Environmental Compliance Coordinator (Contractor) supports the Endoscopy Divisions Product Environmental Compliance program by helping ensure products meet global environmental regulations such as RoHS, REACH, POPs, WEEE, and California Proposition 65.
NewCorporate Affairs Strategist Vistra CorpCorporate Affairs StrategistIrving, TXProvide well-written, researched, validated, clear, consistent business communications on a range of topics that span company announcements, leadership communication, meeting presentations, multimedia, scripts, key messages, and talking points. Corporate Affairs strategists will have depth of experience in all aspects of corporate affairs: communications, community affairs, corporate giving, and media relations.
SVP, Federal Affairs TalentRemedySVP, Federal AffairsArlington, TexasServe as a leading industry spokesperson, issue expert and thought leader on policy issues relating to nutrition, ingredient safety, consumer transparency, and chemicals management on behalf of the association/industry in media interviews, external events and other communications forums. Oversee key internal member communities, including the Food and Beverage Strategy Group, Household and Personal Care Strategy Group, Federal Affairs committee and related exchanges, including soliciting executive engagement.
Director, Government Affairs Heidelberg Materials AGDirector, Government AffairsIrving, TX$172,170–$229,563.32 / yearPartner cross-functionally with legal, operations, communications, sustainability, commercial, and other business teams to align public policy strategies with business goals and provide actionable policy insights. Minimum of 10 years of experience in government affairs, public policy, advocacy, or a related field, preferably within the building materials, construction, manufacturing, industrial, or related sectors.
Director, Government Affairs Heidelberg Materials US, Inc.Director, Government AffairsIrving, TXPartner cross-functionally with legal, operations, communications, sustainability, commercial, and other business teams to align public policy strategies with business goals and provide actionable policy insights. **What You'll Be Doing** + Develop and execute state and regional government affairs strategies that advance business priorities in partnership with regional leadership teams.
Corporate Affairs Strategist VistraCorporate Affairs StrategistIrving, Texas5+ years of relevant work experience in communications, public relations, journalism •Experience in government, regulatory, or public issues communications •Excellent written and verbal communication skills •Familiarity with photography and videography a plus •Ability to detect issues and correctly interpret and communicate information •Strong knowledge and awareness of corporate communications and news media •Knowledge of energy industry and/or competitive businesses •Experience gained through college degree programs and/or certifications is applicable to above skills •Self-managed overnight travel required •HS Diploma or equivalency Key Metrics . •Provide well-written, researched, validated, clear, consistent business communications on a range of topics that span company announcements, leadership communication, meeting presentations, multimedia, scripts, key messages, and talking points.
Director, Government Affairs Heidelberg MaterialsDirector, Government AffairsIrving, TexasPartner cross-functionally with legal, operations, communications, sustainability, commercial, and other business teams to align public policy strategies with business goals and provide actionable policy insights. Minimum of 10 years of experience in government affairs, public policy, advocacy, or a related field, preferably within the building materials, construction, manufacturing, industrial, or related sectors.
NewSenior Director Corporate Affairs Bimbo CanadaSenior Director Corporate AffairsIrving, TX$105,100–$147,100 / yearLead the development of high-impact content for internal and external audiences - including executive communications, town hall materials, corporate narratives, press materials, digital content, and leadership messaging - ensuring every output is clear, on-brand, and purpose-driven. The successful candidate brings deep experience communicating to and through large, distributed and frontline workforces and is equally at home advising executives, directing a crisis response, or developing communications that reach a manufacturing floor.
NewGovernment Affairs & Strategic Partnerships Jr. Manager Flix SEGovernment Affairs & Strategic Partnerships Jr. ManagerDallas, TXYou will develop strategic partnerships with public and private entities, navigate complex government processes, and ensure compliance while establishing access to high-value transportation hubs across the country. Manager, you will support market expansion by securing access to critical infrastructure, managing relationships with key stakeholders, and driving operational success in a highly regulated environment.
NewGovernment Affairs & Strategic Partnerships Jr. Manager FlixGovernment Affairs & Strategic Partnerships Jr. ManagerDallas, TXYou will develop strategic partnerships with public and private entities, navigate complex government processes, and ensure compliance while establishing access to high-value transportation hubs across the country. Manager , you will support market expansion by securing access to critical infrastructure, managing relationships with key stakeholders, and driving operational success in a highly regulated environment.
Regulatory Compliance Specialist The Hire SolutionRegulatory Compliance SpecialistDallas, TexasRemoteThe successful candidate will have experience working with regulatory documentation, supplier relationships, and supply chain processes, preferably within the chemical, personal care, cosmetic, pharmaceutical, or related industries. A growing specialty chemical distribution company is seeking a highly organized and detail-oriented Regulatory Affairs Specialist to join its team.
Research Regulatory Compliance Manager Methodist Health SystemResearch Regulatory Compliance ManagerDallas, TXOur reputation as an award-winning employer shows in the distinctions we've earned: • Great Place to Work Certified 2026-2027 • Glassdoor's Best Places to Work 2025 & 2026 • Glassdoor's Best Places to Work in Healthcare, Biotech & Pharma 2026 • TIME's Best Companies for Future Leaders 2025 & 2026 • Newsweek's America's Most Admired Workplaces 2026 • Glassdoor's Best-Led Companies 2025 • Fortune Best Workplaces in Health Care 2025 • Military Friendly Gold Employer 2025 • Becker's Hospital Review 150 Top Places to Work in Healthcare 2025 • Newsweek's Americas Greatest Workplaces 2025. Named one of the fastest-growing health systems in America by Modern Healthcare, Methodist has a network of 12 hospitals (through ownership and affiliation) with nationally recognized medical services, such as a Level I Trauma Center, multi-organ transplantation, Level III Neonatal Intensive Care, neurosurgery, robotic surgical programs, oncology, gastroenterology, and orthopedics, among others.
Regulatory Compliance Officer - (108090) SanminaRegulatory Compliance Officer - (108090)Carrollton, TXRecognized as a technology leader, SanminaCorporationprovides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors. Job DescriptionSanmina Corporation (Nasdaq: SANM) is a leading integrated manufacturing solutions provider serving the fastest-growing segments of the global Electronics Manufacturing Services (EMS) market.
Regulatory Manager Marmon Holdings IncRegulatory ManagerAddison, TXThe RM provides regulatory leadership and ensures compliance with all regulatory applications including submissions, managing departmental projects, creating, and reviewing labeling, interacting with governmental agencies, and directing and managing department employees. Oversee subordinates in the preparation, organization, coordination of content/data and ensure regulatory compliance for submission to the FDA or regulatory agencies (e.g., 510(k), PMA, MDD/MDR Technical Files/Design Dossiers, global registration applications, etc.).
Regulatory Compliance Officer Sanmina CorpRegulatory Compliance OfficerCarrollton, TXRecognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors. Sanmina Corporation (Nasdaq: SANM) is a leading integrated manufacturing solutions provider serving the fastest-growing segments of the global Electronics Manufacturing Services (EMS) market.
NewRegulatory Compliance Lead Verily Life Sciences LLCRegulatory Compliance LeadDallas, TXDemonstrated technical experience developing regulatory compliance frameworks for SaMD and/or AI/ML-enabled products, with working knowledge of applicable FDA guidance including FDA QMSR, and familiarity with ISO 13485:2016 requirements, risk management processes per ISO 14971 and medical device software lifecycle processes per IEC 62304. Experience with AI/ML-enabled medical device products, including familiarity with FDA AI/ML SaMD guidance, predetermined change control plans (PCCP), and post-market performance monitoring for generative AI applications; experience using generative AI tools (e.g., Claude, ChatGPT) to enhance regulatory and compliance workflows is a plus.
Senior Manager ? Bank Regulatory Compliance Officer Madison-DavisSenior Manager ? Bank Regulatory Compliance OfficerDallas, TXThe successful candidate will work closely with business leaders, Legal, Risk, Audit, and Compliance partners to strengthen regulatory frameworks, support remediation efforts, and ensure compliance programs remain aligned with evolving supervisory expectations. A global financial institution is seeking an experienced regulatory compliance professional to join a strategic Compliance Initiatives and Advisory team supporting wholesale banking and capital markets businesses.
Compliance Manager - Regulatory Obligations Madison-DavisCompliance Manager - Regulatory ObligationsDallas / Fort Worth, TXThis role will focus on maintaining regulatory inventories, tracking regulatory developments, supporting compliance change initiatives, and ensuring regulatory requirements are appropriately reflected within policies, controls, and business processes. The successful candidate will work closely with Compliance, Legal, Risk, Audit, and business stakeholders to strengthen regulatory governance, improve traceability of obligations, and support enterprise compliance initiatives.
Legal Engineering Manager, In-House (Litigation/Regulatory) Counsel AI CorpLegal Engineering Manager, In-House (Litigation/Regulatory)Dallas, TX$315,000–$385,000 / yearIn addition to managing and developing the team, you will work directly with strategic customers, help shape Harvey's go-to-market approach, and partner cross-functionally with Product, Marketing, Enablement, and Engineering to improve how Harvey serves the legal industry. Qualified lawyer with 7+ PQE, including significant experience practicing litigation, regulatory, investigations, compliance, white-collar defense, enforcement, employment litigation, financial regulatory matters, government investigations, or other contentious legal work, including experience working in-house.
Legal Engineering Manager, In-House (Litigation/Regulatory) HarveyLegal Engineering Manager, In-House (Litigation/Regulatory)Dallas, TexasIn addition to managing and developing the team, you will work directly with strategic customers, help shape Harvey’s go-to-market approach, and partner cross-functionally with Product, Marketing, Enablement, and Engineering to improve how Harvey serves the legal industry. Qualified lawyer with 7+ PQE, including significant experience practicing litigation, regulatory, investigations, compliance, white-collar defense, enforcement, employment litigation, financial regulatory matters, government investigations, or other contentious legal work, including experience working in-house.
Senior Compliance Analyst - Regulatory Exams Cetera Financial Group IncSenior Compliance Analyst - Regulatory ExamsDallas, TX$82,000–$117,000 / yearCetera Financial Group" refers to the network of independent retail firms encompassing, among others, Cetera Advisors LLC, Cetera Wealth Services LLC (f/k/a Cetera Advisor Networks), Cetera Investment Services LLC (marketed as Cetera Financial Institutions, or Cetera Investors. About Cetera Financial Group: Cetera Financial Group ("Cetera") is a leading network of independent retail broker-dealers empowering the delivery of objective financial advice to individuals, families and company retirement plans across the country through trusted financial advisors and financial institutions.
Regulatory & Clinical Specialist LivaNova PlcRegulatory & Clinical SpecialistDallas, TXRemote$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. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for "See Open Jobs" on https://www.livanova.com/en-us/careers , and check that all recruitment emails come from an @livanova.com email address.
Team Lead- Regulatory- Homeowner Advocacy NewRez LLCTeam Lead- Regulatory- Homeowner AdvocacyCoppell, TXWhether currently serving as a written, verbal, credit reporting, or special loans specialist, the Team Lead for Homeowner Advocacy remains dedicated to efficiently managing their primary workload of resolving routine tasks. The Team Lead - Homeowner Advocacy is a highly experienced specialist with a proven track record in managing homeowner-related issues.
Associate Dean Academic Affairs/Workforce Programs Collin CollegeAssociate Dean Academic Affairs/Workforce ProgramsFrisco, TXServe as liaison between the academic division and various departments, programs, and services to coordinate dual credit offerings, service learning, the honors institute, and honor societies. Required & Preferred Qualifications (if applicable): The intent of this job description is to provide a representative summary of the types of duties and responsibilities that will be required of the positions given this title and shall not be construed as a declaration of the specific duties and responsibilities of any particular position.
Regulatory Correspondence Specialist III NewRez LLCRegulatory Correspondence Specialist IIICoppell, TXRequires continuous learning and keeping up to date with the Regulations related to the Real Estate Settlement Procedures Act ("RESPA"), Truth in Lending Act ("TILA") the Fair Credit Reporting Act ("FCRA"), the Consumer Financial Protection Bureau ("CFPB"), and policies and procedures regarding Fraud/ID Theft. The Regulatory Correspondence Specialist III is adequately experienced to decipher the homeowner's complaint to the point of identifying the exact issues, identifying root cause, and determining corrective action and next steps.
REGULATORY SPECIALIST - CRI Methodist Health SystemREGULATORY SPECIALIST - CRIDallas, TXYour Job Requirements: • Bachelor''s degree required; Master's degree preferred • CCRC or CCRP (preferred) • GCP certification (preferred) • 1 year of experience in a medical or clinical setting (required) • 1 year of experience in clinical research (required) • 1 year of experience in research regulatory affairs (required) • Strong proficiency using Microsoft Office products • Superior oral and written communication skills • Strong process orientation • Detail oriented, logical, and methodological approach to problem solving • Ability to provide vision and leadership. Your Job Responsibilities: • Communicate clearly and openly • Build relationships to promote a collaborative environment • Be accountable for your performance • Always look for ways to improve the patient experience • Take initiative for your professional growth • Be engaged and eager to build a winning team • Review clinical research protocols to determine logistical components of regulatory requirements • Obtain and facilitate tracking of relevant regulatory documents for clinical trials submission and management.
Regulatory Specialist - Cri Methodist Health SystemRegulatory Specialist - CriDallas, TexasYour Job Requirements: • Bachelor's degree required; Master’s degree preferred • CCRC or CCRP (preferred) • GCP certification (preferred) • 1 year of experience in a medical or clinical setting (required) • 1 year of experience in clinical research (required) • 1 year of experience in research regulatory affairs (required) • Strong proficiency using Microsoft Office products • Superior oral and written communication skills • Strong process orientation • Detail oriented, logical, and methodological approach to problem solving • Ability to provide vision and leadership. Your Job Responsibilities: • Communicate clearly and openly • Build relationships to promote a collaborative environment • Be accountable for your performance • Always look for ways to improve the patient experience • Take initiative for your professional growth • Be engaged and eager to build a winning team • Review clinical research protocols to determine logistical components of regulatory requirements • Obtain and facilitate tracking of relevant regulatory documents for clinical trials submission and management.
Regulatory Compliance Specialist CornerStone Professional PlacementRegulatory Compliance SpecialistFort Worth, TX$30–$34 / hourAdditionally, the specialist will collaborate with cross-functional teams to enhance operational systems, improve data quality, and drive process efficiencies across compliance-related programs. The Regulatory Compliance Specialist will partner closely with the Operations Senior Manager to support the execution, monitoring, and continuous improvement of compliance programs and operational processes.
Financial Institution Regulatory Compliance Senior Consultant Baker Tilly Advisory Group, LPFinancial Institution Regulatory Compliance Senior ConsultantFrisco, TexasBaker Tilly Advisory Group, LP and Baker Tilly US, LLP, trading as Baker Tilly, are independent members of Baker Tilly International, a worldwide network of independent accounting and business advisory firms in 141 territories, with 43,000 professionals and a combined worldwide revenue of $5.2 billion. Baker Tilly is a leading advisory, tax and assurance firm, providing clients with a genuine coast-to-coast and global advantage in major regions of the U.S. and in many of the world's leading financial centers - New York, London, San Francisco, Los Angeles, Chicago and Boston.
Manager, Regulatory Compliance Abbott LaboratoriesManager, Regulatory CompliancePlano, TX$99,300–$198,700 / yearOur portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
NewManager, Regulatory Compliance AbbottManager, Regulatory CompliancePlano, TexasContinuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day) . Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Senior Regulatory Compliance Specialist, Trust & Safety (Temporary - 6 month) Match Group IncSenior Regulatory Compliance Specialist, Trust & Safety (Temporary - 6 month)Dallas, TX$145,000–$180,000 / yearYou should be comfortable working independently with open-ended projects, and engaging with highly sensitive subject matter (with potential exposure to sensitive visual content) as part of the Trust & Safety team. Beyond documentation, we're looking for a hands-on changemaker who can identify the next steps needed to meet both the letter and spirit of evolving global regulatory requirements, and convey those next steps to product teams.
Sr Regulatory Product Compliance Specialist Motorola Solutions IncSr Regulatory Product Compliance SpecialistAllen, TX$98,100–$156,200 / yearRF: FCC Part 15 Subparts C, D, E, F, FCC Parts 22, 25, 90, 96, FCC RF Exposure Compliance, RSS-102, RSS-247, RSS-210, RSS-195, RSS-119, RSS-132, RSS-131, RSS-139, RSS-220, RSS-140, RSS-GEN, EN 300 328, EN 300 220, EN 300 440, EN 301 893, EN 301 908, EN 62479. Whether its helping firefighters see through smoke, enabling police officers to see around street corners, or reliably keeping the lights on in homes and businesses around the world, our work supports those who put their lives on the line to keep us safe.
Senior Project Manager, Clinical Risk Evaluation Abbott LaboratoriesSenior Project Manager, Clinical Risk EvaluationPlano, TX$78,000–$156,000 / yearFacilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P and Marketing, Library Services, Quality Engineering, Post-market Surveillance Group, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers). The CRE Program Manager writes and manages risk evaluation files, performs risk analysis, manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables.
Senior Project Manager, Clinical Risk Evaluation AbbottSenior Project Manager, Clinical Risk EvaluationPlano, TexasFacilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P and Marketing, Library Services, Quality Engineering, Post-market Surveillance Group, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers). The CRE Program Manager writes and manages risk evaluation files, performs risk analysis, manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables.
Clinical Study Manager Argon Medical Devices IncClinical Study ManagerPlano, TexasFull timeThe CSM collaborates closely with cross‑functional partners including Regulatory Affairs, Quality, Medical Affairs, and Product Development to generate high‑quality clinical evidence that supports product safety, performance, and regulatory objectives. Position Overview: The Clinical Study Manager (CSM) is responsible for the planning, execution, and oversight of clinical investigations for medical devices across the product lifecycle, including pre‑market and post‑market studies.
NewClinical Strategy Lead Argon Medical Devices IncClinical Strategy LeadPlano, TexasFull timeThis role partners Clinical Affairs, Regulatory Affairs, R&D, Marketing, and Medical Affairs to identify evidence gaps, evaluate clinical opportunities, and design studies that support product development, regulatory submissions, market access, and commercial objectives. The Clinical Strategy Lead serves as the clinical architect for prospective studies, retrospective studies, investigator-initiated studies, post market studies, and new product development initiatives.
NewRare Disease Medical Science Liaison- South Central Kyowa Kirin Pharmaceutical Research IncRare Disease Medical Science Liaison- South CentralDallas, TX$170,000–$195,000 / yearServe as a trusted scientific expert by engaging in compliant, peer-to-peer scientific exchange and providing accurate, balanced, and evidence-based medical and clinical information regarding Kyowa Kirin products, disease states, and emerging clinical data, including responses to unsolicited medical information requests. Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.
NewAssociate Director, Corporate Compliance Oscar Health IncAssociate Director, Corporate ComplianceDallas, TXRemote$134,136–$176,053 / yearAbout the role: The Associate Director, Corporate Compliance is responsible for training, investigating, monitoring, and enforcing, when necessary, programs, policies, and practices to ensure all applicable operational functions are in compliance with federal, state and local regulatory requirements. Partner with Risk and Controls to manage regulatory risk sustainably while deploying scalable compliance functions that support Oscar''s technology, strategic partners, and business growth.