Jason Carlson

VP Data Integrity and Gxp Systems @Aqtual, Inc

San Jose, CA, US
EMAILS
j••••••••@aqtual.com
MOBILE NUMBERS
+16•••••••98

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WORK HISTORY

Apr 2024 — Present

VP Data Integrity and Gxp Systems @Aqtual, Inc

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Hayward, CA, US

Accountable for leading and working alongside multidisciplinary team members within and external to the organization (clinical study sites, research partners, technology vendors) to achieve and sustain data quality and systems compliance, supporting the total lifecycle of products developed and marketed by Aqtual. Responsibilities and contributions include Clinical Data Science, Data Analysis, Data Visualization/Analytics, Quality, Data Integrity, Compliance, Regulatory, Cybersecurity, Data Protection, Publications, and Product Development.

EDUCATION

2020 — 2022

Imperial College London

Master of Public Health - MPH, Global MPH Program

N/A

University of California, Davis

Genetics, Molecular and Cellular Biology

SKILLS

CdiscSop21 Cfr Part 11Clinical TrialsStatistical ProgrammingU.s. Title 21 Cfr Part 11 RegulationDrug DevelopmentCdisc StandardsGcpSop DevelopmentComputer System ValidationClinical DevelopmentMedidataCRO ManagementIch-GcpOffshore OutsourcingQuality ManagementClinical Data ManagementPlanning Budgeting & ForecastingOracle ClinicalClinical DataEmotional IntelligenceGood Clinical Practice (Gcp)Department Budget ManagementData VisualizationCross Functional Relationship BuildingData QualityCrf DesignData ManagementGlobal Resource ManagementClinical ResearchCROClinical Trial Management System (Ctms)BiomarkersTeam LeadershipStandard Operating Procedure (Sop)MeddraData StandardsEdcCtms

ABOUT JASON CARLSON

Demonstrated success working in a variety of settings, including start-up, biotech, pharma, medical device, consulting, and contract research organizations.Strengths include data science and management with quality and integrity, product development, technical project management, regulatory compliance, cybersecurity and data protection, continuous process improvement, software development, data analytics, exhibiting a sense of shared urgency, leadership, team development, partnership (health systems, academia, providers of solutions and services), standards development, influencing, procedural document development, training, and striving for efficiency.Therapeutic area experience includes oncology, antiviral (HIV, HCV), cardiovascular disease, rheumatoid arthritis, diabetes, respiratory, liver disease, and post-organ transplant immunosuppression. Significant involvement in commercial product development and launches, including: Galleri, Zydelig, Harvoni, Sovaldi, Complera, Stribild, Ranexa, Cellcept.Broad range of experience with the development, evaluation, selection, implementation and/or utilization of software in support of clinical development operations.Partnership with hospital network collaborators to acquire clinical study data from electronic health records, resulting in a significant reduction in the need for manual data entry.Recent conference attendance and participation includes-Society for Clinical Data Management Annual Conference, Oct 2023-Application of Artificial Intelligence and Machine Learning for Precision Medicine, FDA and M-CERSI, Feb 2023-Establishing a High Quality Real World Data Ecosystem, Duke Margolis Center for Health Policy with FDA and Industry Speakers, Jul 2020-Developing Real-World Data and Evidence to Support Regulatory Decision-Making, Duke Margolis Center for Health Policy with FDA Speakers, Oct 2019-FDA Regulatory Education for Industry, Medical Device Track, May 2019-Healthcare Information and Management Systems Society, Feb 2019-FDA & MHRA Good Clinical Practice Workshop: Data Integrity in Global Clinical Trials, Oct 2018-American Society of Clinical Oncology, May 2017-Exponential Medicine Conference, Nov 2015

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