Arick Wong
Clinical Trial Manager @ Vivace Therapeutics, Inc.
About
I lead clinical operations with a focus on scalability, quality, and speed-to-market. With 11 years of progressive experience spanning sponsor, CRO, and site-level roles across oncology, rare disease, infectious disease, CNS, and other indications, I bridge the gap between complex clinical development goals and high-performance operational reality. My career is defined by a "strategy-first" approach to Phase I-III trials, ensuring that global programs are not only compliant but optimized for cost and timeline efficiencies.- Strategic Versatility: I have steered trials across a massive range of indications—from high-science Oncology and Rare Disease to Cardiology and NASH.- High-Stakes Leadership: Expert at managing large-scale CROs and niche vendors, moving beyond "management" into true partnership and KPI optimization.- Regulatory & Quality Rigor: Expertise in ICH-GCP, global regulatory submissions, and ensuring "inspection-ready" quality for both drugs and IVD medical devices.Clinical Portfolio Highlights:- Oncology & Immunology: Extensive work in Solid & Liquid tumors (mesothelioma, NSCLC, Glioblastoma, Sarcoma, Leukemia/Lymphoma).- Advanced Modalities: Leading-edge research in Stem Cell Therapy (CAR-T, CAR-NK) and Psychedelic Therapeutics (PTSD/Eating Disorders).- Infectious Disease & Vaccines: Rapid-response trial management for HIV, RSV, and Influenza.- Specialized Research: Primary Mitochondrial Disease (Rare Disease), IVD Medical Devices, and Pain Management.I thrive in fast-paced environments where I can develop clinical teams, mitigate operational risks, and drive life-changing therapies toward approval.
United States
San Francisco Bay Area
Biotechnology
Communication, WordPress, Blogging, Video Editing, Graphic Design, SPSS, Research, Editing, Microsoft Office, Statistics, PowerPoint, Social Media, Community Outreach, Public Speaking, Teaching, Microsoft Excel, Event Planning, French, Creative Writing, Photoshop
Experience

Clinical Research Associate
Lucira Health
Emeryville, California
- Developed and implemented in-vitro diagnostic study protocols, leading to successful completed of two medical device trials and assisted in one regulatory submission through the 510k/CLIA pathway. - Managed multiple trial budgets (~$400,000-$2,500,000), reviewed and approved invoices, and drafted clinical study budgets. - Performed site selection, investigator qualification, and site initiation trainings and created source documentation, study protocols, and informed consent forms, and other patient-facing materials. - Analyzed clinical trial data and prepared presentations for board meetings, investors, and various external parties. - Created and managed department electronic data capture system. - Assisted in the creation of a clinical quality management system; drafted new standard operating procedures for IP management, data management, and the clinical trial implementation process.
Arick Wong's Contact Information
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