Matthew Thompson Email and Phone Number
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Passionate and solution-driven professional with 15+ years of experience in management consulting, with a specialization in life sciences strategy. Expertise includes commercial strategy, regulatory compliance, and business development. Proven track record of leading diverse teams and exceeding performance targets while promoting a positive culture. Adept at cultivating relationships with team members and multilevel stakeholders to drive organizational growth. Core Competencies: Global Product Launches | Commercial Strategy | Regulatory Strategy | Budgeting & Forecasting | Revenue Growth | Strategic Leadership | Process Improvement | Training & Development | Conflict Resolution | Diversity, Equity & InclusionHighlights: • Developed and led numerous short- and longer-term C-suite mandated projects, including product and portfolio regulatory strategy, organizational redesign, and strategy implementation• Trusted advisor to leading, global life sciences companies, providing ongoing support for strategy, portfolios, and products• Assessed and implemented strategies to maximize value for research pipelines and commercial portfolios• Provided extensive merger and acquisition support, including leading global regulatory assessment, strategy development, and post M&A implementation for news-leading deals––leading cross-functional team in due diligence, transition, and post-transition • Led strategic update and organizational change projects for a leading life science companies’ business-critical function• Led strategic assessments and organizational development of multiple biotech and pharma clients’ global core functions (e.g., Commercial, Marketing, Healthcare Compliance, Regulatory Affairs)• Served as subject matter expert and “issue resolution specialist” for client leaders across the life sciences industry
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Regulatory Strategy ConsultantMt Pharma Consulting LlcWest Hollywood, Ca, Us
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Ceo, Life Sciences Strategy ConsultantMt Pharma Consulting Llc Jun 2014 - PresentLos Angeles, California, UsLaunched and managed full cycle operations of a consultancy which specializes in life sciences––built and serviced a portfolio of 15+ industry leading clients in the pharmaceuticals, biotechnology, and medical device sectors • Spearheaded 50+ client engagements since 2014, with budgets of up to $800K in client billings per project • Sourced, hired, and collaborated with independent consultants to ensure streamlined project delivery Project Highlights: • Served on cross-functional functional leadership team for high profile commercialization of global portfolio––led commercial organization buildout, brand and franchise organizational implementation, and commercial & regulatory strategy • Led multi-year commercial and marketing efforts for patient and HCP messaging and education––specifically for common device constituent platform utilized across a leading biotech company’s core franchise• Managed assessment, strategy, and planning for digital health integration (e.g., connected devices, telehealth, diagnostics) for first-in-class chronic disease management• Supported high-profile M&A due diligence, transition, and post-transition regulatory projects involving industry leading portfolios• Served as on leadership team for leading drug/device combo manufacturer––leading organizational strategic change efforts, aligning commercial and regulatory needs, and implementing streamlined commercial processes • Performed regulatory assessment of a high-profile global portfolio by identifying, categorizing, planning, and remediating key value-chain/process failures, functional and organizational issues, and globally derived barriers to business • Collaborated with executives to redesign a therapeutic area portfolio to maximize value and support regulatory/commercials success• Assessed product global regulatory landscape and designed regulatory strategy for global product expansion
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Executive Director, Regulatory AffairsVeru Inc. Jun 2022 - May 2023Miami, Fl, UsGlobal Regulatory Affairs and Brand Teams leader, overseeing evolving portfolio consisting of pharmaceutical and device assets. Global organizational leader – with oversight of global regulatory strategy, systems, and processes development and implementation – with ~ 15 global teams with direct reports (FTE, augment staff, and consulting groups), overseeing and ensuring quality and completeness of all OUS regulatory submissions. Integrated leader for global commercialization efforts (e.g. marketing, legal, and regulatory integrated projects), global medical education foundation, integrated leadership with supply chain (e.g., GDP, GMP) development and pharmacovigilance to support commercialization and certifications as needed; integrated leadership with global clinical trial programs, and broader organizational development, compliance, and readiness projects. -
ManagerPwc Jan 2011 - May 2014GbManaged a multi-mulligan dollar annual portfolio of client engagements––directly serving point of contact with executive management for top-tier life sciences companies• Oversaw multiple domestic and international projects to assess, update, and support regulatory and compliance standards and client project requirements • Conducted assessments for 20+ top-tier pharmaceutical and medical device clients to analyze enterprise risk• Partnered with Executive Leaders to define, develop, and deliver short- and longer-term executive, functional, programmatic, resourcing, and partnership roadmaps • Served as interim compliance lead––defining strategic program development of high-profile client’s global compliance programs• Developed portfolio of successfully implemented global policies and procedures for numerous Life Science Companies• Led executive, clinical, commercial, and compliance leaders in aligning business operations and standards to mitigate global risks • Supported multiple Life Science companies as OIG required Compliance Expert––assessing the current compliance internal processes against regulatory and CIA requirements, and provided strategic recommendations to improve processes -
ManagerDeloitte & Touche Llp Aug 2010 - Dec 2010Worldwide, OoConducted internal assessments for various pharmaceutical network and medical device clients to identify, assess, and prioritize organizational and function-specific risk and developed mitigation strategies • Developed regulatory and compliance guidance documents and trainings for pharmaceutical and medical device organizations• Managed a global portfolio of projects and client engagements––overseeing individual workstream staff of 50+• Conducted extensive assessments of regulatory documentation for submission accuracy, submission completeness, substantial evidence, appropriate referencing, and applicable internal tracking mechanisms documentation -
Senior ConsultantDeloitte & Touche Llp Aug 2008 - Aug 2010Worldwide, Oo• Managed multinational assessment of a pharmaceutical manufacture’s regulatory processes and provided key recommendations• Updated all regulatory files for medical device portfolio related to applicable country-specific regulations and supported submissions to applicable regulatory bodies • Developed and drafted regulatory affairs and operations SOP manual for a pharmaceutical company’s global footprint• Led re-engineering of a mid-size pharmaceutical organization’s Regulatory Affairs department––including assessment and updates of internal guidance documents • Partnered with leading organizations to support OIG investigations with inside/outside counsel on issues related to operational aspects impacting billing and regulatory issues
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ConsultantDeloitte & Touche Llp Jan 2007 - Aug 2008Worldwide, Oo• Developed and drafted core documentation SOP Manual for healthcare provider and device organization• Developed compliance function structure for a nationally ranked hospital organization • Trained and managed 8 team members from counsel on medical record review processes • Conducted due diligence assessments of potential acquisitions and partnering organizations
Matthew Thompson Skills
Matthew Thompson Education Details
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University Of Missouri-ColumbiaHealthcare -
University Of Missouri-ColumbiaPsychology
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University Of Missouri-Kansas CityMedicine (Md Studies)
Frequently Asked Questions about Matthew Thompson
What company does Matthew Thompson work for?
Matthew Thompson works for Mt Pharma Consulting Llc
What is Matthew Thompson's role at the current company?
Matthew Thompson's current role is Regulatory Strategy Consultant.
What is Matthew Thompson's email address?
Matthew Thompson's email address is ma****@****mac.com
What is Matthew Thompson's direct phone number?
Matthew Thompson's direct phone number is +161784*****
What schools did Matthew Thompson attend?
Matthew Thompson attended University Of Missouri-Columbia, University Of Missouri-Columbia, University Of Missouri-Kansas City.
What are some of Matthew Thompson's interests?
Matthew Thompson has interest in Economic Empowerment, Civil Rights And Social Action, Politics, Science And Technology, Human Rights, Arts And Culture, Health.
What skills is Matthew Thompson known for?
Matthew Thompson has skills like Strategy, Management Consulting, Management, Program Management, Leadership, Due Diligence, Business Process Improvement, Regulatory Affairs, Risk Management, Policy, Healthcare, Medical Devices.
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