Chaz Stephens
Program manager and PMP interested in product development: identifying market gaps and building the strategy to close them.
I've spent over a decade in and around cancer biology. It started with graduate research on TGF-β signaling in fibrosis and cancer, then became a run of program management roles: overseeing cancer clinical trials at the National Cancer Institute, cancer diagnostics at Quest Diagnostics, and now broader clinical data standards work at Merck. What's kept me in this space is the patient population at the other end of it: clinical trials and diagnostics only matter because someone is waiting on the result.
What I've found I enjoy most, though, is owning that whole arc myself: taking a product from an idea through to a real commercialization strategy, not just one piece of it. A hands-on product management course let me build a full example of that, end to end, and produced the SubQ-Confirm case study below: market sizing, product requirements, and a go-to-market plan for a real patient-facing need. I hold a patent and three peer-reviewed publications from my earlier research, and I write Indigo & Asphalt, an independent menswear publication, on the side.
Turning clinical complexity into concrete product decisions.
From bench science to shipped product.
Led the company-wide SDTM Implementation Guide v3.4 rollout and direct the cross-functional governance network for immunology and vaccine clinical data.
Oversaw cross-functional teams delivering cancer diagnostic products from concept through post-launch.
Managed biomarker studies and clinical trial operations for the Cancer Therapy Evaluation Program across 100+ trials, recognized with NCI's Distinguished Achievement Award in 2018 and 2020.
Supported assay transfer, validation, and quality control across all phases of contract lab work.
Served as point-of-contact project manager for pharmaceutical clients' xenograft studies, from proposal through execution.
- PMP-certified
- Agile & Waterfall
- Product requirements definition
- Market sizing & competitive analysis
- Go-to-market strategy
- Cross-functional governance leadership
- FDA 510(k) pathway
- ICH/GCP compliance
- Risk & human-factors analysis
- Clinical data standards (SDTM)
- Web + Android product development
- Stripe billing integration
- End-to-end product ownership
- Practical use of AI tools (Claude, Gemini, Copilot) in daily workflow
- Google Cloud Certified Generative AI Leader