Hire the Best Regulatory Compliance Freelancers in New York

I build the systems, then document them for compliance. Most AI governance help is one or the other: policy consultants who can't read your codebase, or engineers who've never mapped a control. I do both, and I hold the IAPP AIGP. What I work on: EU AI Act readiness. Article 50 transparency obligations took effect 2 August 2026 and apply now to anyone shipping generative, conversational, or synthetic-media systems into the EU. Article 50(2) marking requirements reach existing systems on 2 December 2026. High-risk obligations were deferred to December 2027, which is a readiness window rather than a reprieve, and the inventory and classification work has to start well before then. Conformity documentation. I built a .NET application that generates structured conformity documentation from model artifacts, with a calibration harness that scores output against reference documents so reliability is measured rather than assumed. I can do this work manually for your systems or help you stand up something similar internally. Framework mapping. Hands-on NIST AI RMF assessments and ISO/IEC 42001 control mapping, including where the two overlap so you're not maintaining parallel evidence for both. The engineering underneath. Production C#/.NET services, Azure, Kubernetes, and Terraform, delivered under regulated change control with enforced separation of duties and tamper-evident change history. Governance advice that ignores how software actually ships tends to produce documents nobody can implement. Good fits: AI Act gap assessments, model documentation and technical files, RAI program setup for teams without a dedicated function, or a second opinion on governance work already underway. Send me what you're building and what regulation you're worried about, and I'll tell you honestly whether it's a fit.

I’m a New York–licensed attorney with 5+ years of in-house legal experience supporting fast-paced fintech, real estate, and tech companies. I specialize in drafting, reviewing, redlining, and simplifying commercial contracts, privacy policies, and terms of use, so founders, operators, and lean teams can move quickly with confidence and clarity. I’ve reviewed hundreds of agreements across a range of business functions and frequently draft user-friendly terms & conditions for marketing and promotional campaigns, privacy policies, and terms of use, balancing compliance with clarity to avoid confusing customers or triggering legal risk. Contracts and Documents I Assist With: • NDAs • MSAs • SaaS Agreements • Licensing & Partnership Agreements • SOWs • Lead Generation Agreements • Employment & Contractor Agreements • Promotional Terms & Conditions • Privacy Policies and Terms of Use • Corporate Resolutions Services I Offer: • Contract redlines with plain-language explanations • Deal risk spotting, negotiation levers, and structure feedback • Compliance checklists and process optimization • Privacy Policy and Terms of Use drafting and reviewing • Fast turnaround available (24hr rush supported) Note: I provide contract consulting and legal drafting, not formal legal representation. I am licensed in New York. Let’s make your contracts, polices, and terms work for your business, clearly, efficiently, and with minimal friction.

CEO of Health Futures Consulting LLC with an MPH in Health Policy from Yale University and 10 years of experience in healthcare consulting, compliance and policy development, public health research, data analysis, and program evaluation. ​​Supporting startup healthcare agencies and established organizations is my specialty and I've guided now multi-million dollar practices get to where they are today! Trained as a health policy compliance professional and a health care consultant, I have earned my expertise through working for powerful federal agencies (CDC, CMS), advising large state departments of health and governing officials (New York, Kentucky, Connecticut), top healthcare management consulting firms, working on research at academic institutions like Yale and Columbia University, and guiding local community-based healthcare organizations. -----------------------------------------------Services Offered---------------------------------------------------- POLICY & COMPLIANCE ✅Custom Policy and Procedure Manual Development, Revisions, and SOPs** ✅ Guiding healthcare agencies with Compliance, Growth, and Business Optimization ✅ HIPAA Compliance** ✅Health and Safety Plans and Trainings (OSHA compliant)** ✅State and Federal Compliance for healthcare organizations ✅ Advisory and Compliance Document Review ✅ Audit readiness ✅ Accreditation Readiness (Joint Commission, ACHC, CARF) ✅Medicaid/Medicare Expertise HEALTHCARE CONSULTING ✅Healthcare Business Optimization + Improvement ✅ Project Management ✅Training, Technical Assistance, and Program Support ✅Quality Improvement- analyzing workflows and providing process improvement support, ways to make your organization more efficient ✅Program Development & Evaluation ✅Engaging Partners and Stakeholders- creating coalitions and facilitating partnerships RESEARCH, WRITING, AND DATA ✅Survey Design- quantitative and qualitative data, and can use Qualtrics, Survey Monkey, LimeSurvey, RedCap, and more ✅Technical Writing- literature reviews, academic writing, writing articles on health-related topics, reports, surveys and questionnaires ✅Grant Writing and Proposals ✅Data Analytics- using your organization’s data to evaluate areas of improvement and strategize solutions. Excellent with advanced data analytic software and skills (R, SPSS, Excel, Dedoose, nVivo, Atlas.ti) ✅Data Visualization- creating compelling graphs, charts, infographics, presentations, dashboards (Excel, Tableau) ✅Data Collection and Cleaning If you require high-quality professional work that is backed by in-depth healthcare knowledge and delivered in a timely manner, look no further! With my Ivy League educational background coupled with skills I honed directly from nationally renowned and esteemed leaders in the field, you can benefit from my expertise today! Let me take your organization to the next level📈 ------------------------------------------ Working With Me Looks Like------------------------------------------ ✅Initial Consultation: We begin with a thorough discussion to understand your project needs and goals. ✅Customized Solutions: I develop a tailored strategy specifically designed for you. ✅Regular Updates: You'll receive consistent updates to ensure all project milestones are being met and to keep you informed of progress.

With an extensive background in FDA regulations and compliance, I am a seasoned professional dedicated to ensuring top-notch standards in FDA regulatory affairs. I have a proven track record of collaborating effectively with the FDA, ensuring compliance, and swiftly implementing corrective actions during inspections. My commitment to transparency and excellence has fortified my reputation as a reliable specialist in regulatory compliance and project management. In addition to my regulatory expertise, I bring a wealth of experience in translating complex legal and technical documents, drafting precise legal materials, and designing FDA-compliant labels. My analytical and problem-solving skills, coupled with a passion for continuous improvement, make me a valuable asset to any organization striving for excellence in compliance and safety.

I am a skilled and experienced biomedical engineer specializing in the design and development of medical devices/medical technologies. I have worked in the medical technology industry for over a decade and have a Bachelors of Engineering and Masters of Science in biomedical engineering. With extensive expertise in design quality, quality assurance, and regulatory affairs within the industry, I am well-equipped to handle any challenges that may arise. Throughout my career, I have successfully worked with both large medical device corporations and startups, gaining invaluable insights into the FDA submission process and the specific requirements based on technology risk. I possess a thorough understanding of how to navigate the complex regulatory landscape and bring medical devices through the approval process. My previous accomplishments include the development and maintenance of robust quality systems, leading design quality projects for Class II/III medical devices by employing risk analysis and design control strategies. Additionally, I have extensive experience in interacting with the FDA throughout the pre-submission and 510(k)/PMA/De Novo submission processes, ensuring compliance and smooth communication. Furthermore, I am well-versed in auditing quality systems based on 21 CFR 820 and ISO 13485. This ensures that my clients can confidently rely on my expertise to meet and exceed regulatory requirements and industry best practices. If you are in need of a highly skilled MedTech consultant with a proven track record and in-depth knowledge of the medical technology industry, I am confident that my qualifications make me the ideal candidate for your project. Let's collaborate to bring your ideas to life and transform healthcare for the better.

I’m a former Chief Compliance Officer for a global cross-border payments provider with over 10 years of exposure in the compliance space. During my tenure as CCO I gained extensive experience in building and maturing compliance programs, planning and executing key vendor technical integrations, and forming strong working relationships with US regulators. I’m a collaborative team player accustomed to working with global teams across multiple regions, with a focus on compliance program automation and frictionless operational processes. Compliance Program & Operations • Authored key policies including AML, KYC/CDD, OFAC, and UIGEA policies • Drafted various SOPs including transaction monitoring, customer onboarding, sanctions screening and departmental procedure documents • Developed a robust risk assessment methodology and risk matrix to accurately identify compliance risks posed by the business • Designed and implemented an automated, frictionless, and fully compliant user onboarding experience • Established and deployed AML detection scenarios and business rules to efficiently capture suspicious typologies and behavior • Experienced in setting and tuning screening tools (i.e., OFAC/watchlist) • Developed a regulator approved AML training program including all lesson materials as well as training assessment • Successfully navigated multiple external audits and regulatory exams Licensing & Regulators • Led the acquisition of all US Money Transmitter licenses on behalf of a foreign-owned payments company • Comprehensive knowledge of US regulatory and licensing requirements for payments and crypto companies • Experienced in forming strong relationships with state regulators and understanding how their areas of focus change from one state to the next • Excellent at interpreting regulations and leveraging licensing exceptions where possible • Understands reporting requirements across different state regulators • Effictively maintain US regulatory licensing while staying informed of anticipated regulatory requirement changes Product Development & Vendor Integrations • Headed selection and implementation of key Compliance vendors (i.e., Onboarding/KYC, Transaction Monitoring and Screening, and Anti-Fraud related service providers) • Great at taking business requirements and translating to actionable deliverables for software developers and engineers • Have helped launch two cross-border payment platforms in the US • Experienced in UI/UX testing, bug identification, and overall platform continuity • Managed several third-party vendor API integrations, including the development of key business requirements and UX design • Developed a regulator approved vendor due diligence and management process with accompanying policies, SOPs and vendor questionnaires Business Strategy • Significant exposure to cross-border payment business processes, including revenue creation, target market identification, and business model development • Experienced in drafting business plans used for regulatory licensing and external due diligence purposes • Understands pricing structures and commercials of data providers, with experience in vendor negotiations and MSA execution • Developed a corporate spin-out plan to save the company millions (USD) in additional permissible investment and cash reserve requirements • Knowledged in identifying and onboarding to key banking partners, as well as corporate and custodial bank account setup • Exposure to FinTech accounting processes and GAAP guidelines