Latt Mansor, DPhil

Research Lead at HVMN

San Francisco, California, United States Contact Info
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About

Internationally educated DPhil (PhD) graduate with 8 years of experience in healthcare and pharmaceutical industries. Key skills include good communication and language skills with high impact on critical business decisions, and a proven track record of strong analytical and research skills in producing a complete overview of critical care market in different countries to optimise engagement strategies. Also demonstrated versatility in adapting to multicultural, fast-paced environment while ensuring top quality deliverables under time constraints.

Activity

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Experience

  • Ketone-IQ Graphic

    Research Lead

    Ketone-IQ

    - Present 5 years

    San Francisco Bay Area

  • Co-Founder

    ConfabHealth

    - Present 6 years 8 months

    Kuala Lumpur, Malaysia

    Co-founded a healthtech company, ConfabHealth, and led day-to-day business operations and development. ConfabHealth is a digital health company that specialises in the application of Conversational User Interfaces and Artificial Intelligence to make personal health information more accessible, understandable and actionable for everyone.
    • Led all business discussions and negotiations with multiple stakeholders across the board including laboratories, insurers, government bodies and…

    Co-founded a healthtech company, ConfabHealth, and led day-to-day business operations and development. ConfabHealth is a digital health company that specialises in the application of Conversational User Interfaces and Artificial Intelligence to make personal health information more accessible, understandable and actionable for everyone.
    • Led all business discussions and negotiations with multiple stakeholders across the board including laboratories, insurers, government bodies and healthcare providers
    • Led and initiated grants and funding opportunities for the company
    • Proactively seek out new collaboration and business opportunities in both the private and public sectors
    • Scouted and made decisions in the recruitment of the business development team

  • Holmusk

    Holmusk

    1 year 8 months

    • Holmusk Graphic

      Director, Business Development

      Holmusk

      - 11 months

      Singapore/ Malaysia

      Lead the entire business pipeline pertaining chronic disease management

    • Holmusk Graphic

      Business Developer

      Holmusk

      - 10 months

      Singapore

      Lead business developer to the CEO and responsible for leading multiple projects:

      • Responsible as the project manager in a collaboration project with SingHealth and National Heart Centre Singapore to analyse and provide descriptive and predictive deliverables on clinical and financial data
      • Lead for developing B2B model of the diabetic management program, Glyco Leap, hence driving discussions, collaborations and strategy of the project with clients
      • Set up the Malaysian office…

      Lead business developer to the CEO and responsible for leading multiple projects:

      • Responsible as the project manager in a collaboration project with SingHealth and National Heart Centre Singapore to analyse and provide descriptive and predictive deliverables on clinical and financial data
      • Lead for developing B2B model of the diabetic management program, Glyco Leap, hence driving discussions, collaborations and strategy of the project with clients
      • Set up the Malaysian office within 2 months of starting the job and responsible for the operations, hiring and legal issues of the office.
      • Leading a team of tech developers for a consulting project to create an operational dashboard for the management team of a private hospital to enable extraction of data from their EHR and provide reports

  • University of Oxford Graphic

    DPhil student

    University of Oxford

    - 4 years

    Oxford, United Kingdom

    Full-time DPhil student working on the thesis entitled 'The effect of hypoxia on cardiac metabolism and function in the type 2 diabetic heart'.

  • The Medicines Company

    The Medicines Company

    5 years 3 months

    • The Medicines Company Graphic

      Analyst for ViTA Solutions consulting

      The Medicines Company

      - 4 years 9 months

      Oxford, United Kingdom

      Lead Analyst to the Chief Knowledge and Information Officer and functioned as a core member in global consulting initiatives, producing and presenting data-driven and rigorous analyses for customer engagements internationally.

      • Effectively set up, monitored and managed workflow and payment methods for collaborators and was the main liaison between the team and collaborators such as pharmaceutical companies, IT providers and physicians.

      • USA – Led background analysis of hospitals…

      Lead Analyst to the Chief Knowledge and Information Officer and functioned as a core member in global consulting initiatives, producing and presenting data-driven and rigorous analyses for customer engagements internationally.

      • Effectively set up, monitored and managed workflow and payment methods for collaborators and was the main liaison between the team and collaborators such as pharmaceutical companies, IT providers and physicians.

      • USA – Led background analysis of hospitals engaged and analysed quality measures set by the Centers for Medicare and Medicaid Services (CMS) for Value Based Purchasing, producing a comprehensive view of the IDNs relative competitive landscape.

      • India – Responsible for research and analyses in a 4 person core team leading international work effort with purpose of architecting a protocol for performance improvement in the chest pain pathway. Final outcome of analysis and proposed solution and protocols were presented to Fortis executives and head cardiologist.

      • Australia – Researched and analysed available resources on AR-DRGs, mortality data, expenditures and principal diagnoses to provide an overall view of Australian healthcare including macro schematics.

      • Germany – Investigated, identified and correlated different variables associated with low patient volumes in Vivantes, Berlin Rehabilitation Centres and architected a solution for improved outcomes.

    • The Medicines Company Graphic

      Program Coordinator

      The Medicines Company

      - 7 months

      Parsippany, New Jersey

      • Organised concise, efficient and up-to-date project documentation for project teams.

      • Responsible for ensuring best team meeting practices, including forward-planning agendas, action items tracking, and timely minutes.

      • Maintained and updated Standard Operating Procedure training records of the clinical operations team.

      • Led the development and creation of the company’s Trial Master Files structure and served as key player from the Clinical Operation team to establish…

      • Organised concise, efficient and up-to-date project documentation for project teams.

      • Responsible for ensuring best team meeting practices, including forward-planning agendas, action items tracking, and timely minutes.

      • Maintained and updated Standard Operating Procedure training records of the clinical operations team.

      • Led the development and creation of the company’s Trial Master Files structure and served as key player from the Clinical Operation team to establish a new database system, linking information from all departments.

      • Core member in the clinical operations team and responsible for study start-up activities including gathering regulatory documentations, performing site document reconciliation and managing the trial master file.

Education

Publications

  • Inhibition of sarcolemmal FAT/CD36 by sulfo-N-succinimidyl oleate rapidly corrects metabolism and restores function in the diabetic heart following hypoxia/reoxygenation

    Cardiovascular Research

    AIMS:
    The type 2 diabetic heart oxidizes more fat and less glucose, which can impair metabolic flexibility and function. Increased sarcolemmal fatty acid translocase (FAT/CD36) imports more fatty acid into the diabetic myocardium, feeding increased fatty acid oxidation and elevated lipid deposition. Unlike other metabolic modulators that target mitochondrial fatty acid oxidation, we proposed that pharmacologically inhibiting fatty acid uptake, as the primary step in the pathway, would…

    AIMS:
    The type 2 diabetic heart oxidizes more fat and less glucose, which can impair metabolic flexibility and function. Increased sarcolemmal fatty acid translocase (FAT/CD36) imports more fatty acid into the diabetic myocardium, feeding increased fatty acid oxidation and elevated lipid deposition. Unlike other metabolic modulators that target mitochondrial fatty acid oxidation, we proposed that pharmacologically inhibiting fatty acid uptake, as the primary step in the pathway, would provide an alternative mechanism to rebalance metabolism and prevent lipid accumulation following hypoxic stress.

    CONCLUSIONS:
    Diabetic hearts have limited metabolic flexibility and cardiac dysfunction when stressed, which can be rapidly rectified by reducing fatty acid uptake with the FAT/CD36 inhibitor, SSO. This novel therapeutic approach not only reduces fat oxidation but also lipotoxicity, by targeting the primary step in the fatty acid metabolism pathway.

    See publication
  • Increased oxidative metabolism following hypoxia in the type 2 diabetic heart, despite normal hypoxia signalling and metabolic adaptation

    The Journal of Physiology

    Adaptation to hypoxia makes the heart more oxygen efficient, by metabolising more glucose. In contrast, type 2 diabetes makes the heart metabolise more fatty acids.

    Diabetes increases the chances of the heart being exposed to hypoxia, but whether the diabetic heart can adapt and respond is unknown.

    In this study we show that diabetic hearts retain the ability to adapt their metabolism in response to hypoxia, with functional hypoxia signalling pathways.

    However, the…

    Adaptation to hypoxia makes the heart more oxygen efficient, by metabolising more glucose. In contrast, type 2 diabetes makes the heart metabolise more fatty acids.

    Diabetes increases the chances of the heart being exposed to hypoxia, but whether the diabetic heart can adapt and respond is unknown.

    In this study we show that diabetic hearts retain the ability to adapt their metabolism in response to hypoxia, with functional hypoxia signalling pathways.

    However, the hypoxia-induced changes in metabolism are additive to abnormal baseline metabolism, resulting in hypoxic diabetic hearts metabolising more fat and less glucose than controls. This stops the diabetic heart being able to recover its function when stressed.

    These results demonstrate that the diabetic heart retains metabolic flexibility to adapt to hypoxia, but is hindered by the baseline effects of the disease. This increases our understanding of how the diabetic heart is affected by hypoxia-associated complications of the disease.

    Other authors
    • Keshavi Mehta, Dunja Aksentijevic, Carolyn A. Carr, Trine Lund, Mark A. Cole, Lydia Le Page, Maria da Luz Sou
    See publication
  • Cardiac metabolism in a new rat model of type 2 diabetes using high-fat diet with low dose streptozotocin

    Cardiovascular Diabetology

    To study the pathogenesis of diabetic cardiomyopathy, reliable animal models of type 2 diabetes are required. Physiologically relevant rodent models are needed, which not only replicate the human pathology but also mimic the disease process. Here we characterised cardiac metabolic abnormalities, and investigated the optimal experimental approach for inducing disease, in a new model of type 2 diabetes.

    High-fat feeding in combination with a low dose of STZ induced cardiac metabolic…

    To study the pathogenesis of diabetic cardiomyopathy, reliable animal models of type 2 diabetes are required. Physiologically relevant rodent models are needed, which not only replicate the human pathology but also mimic the disease process. Here we characterised cardiac metabolic abnormalities, and investigated the optimal experimental approach for inducing disease, in a new model of type 2 diabetes.

    High-fat feeding in combination with a low dose of STZ induced cardiac metabolic changes that mirror the decrease in glucose metabolism and increase in fat metabolism in diabetic patients. While low doses of 15–25 mg/kg STZ induced a type 2 diabetic phenotype, higher doses more closely recapitulated type 1 diabetes, demonstrating that the severity of diabetes can be modified according to the requirements of the study.

    Other authors
    • Eileen R Gonzalez, Mark A Cole, Damian J Tyler, Jessica H Beeson, Kieran Clarke, Carolyn A Carr and Lisa Heath
    See publication

Languages

  • English

    Native or bilingual proficiency

  • Malay

    Native or bilingual proficiency

  • Spanish

    Professional working proficiency

  • Cantonese

    Limited working proficiency

  • Thai

    Limited working proficiency

  • German

    Elementary proficiency

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