Launches are won or lost on market access. I have led the market access strategy behind product launches in five therapeutic areas, three of which became blockbusters, and I now do that work part-time for companies that cannot yet justify a full-time hire.
Pharmaceutical, biotech and medtech, 12–36 months from launch.
Market access work should start well before launch. But the only way to get senior market access judgment has usually been to hire for it, and a full-time market access executive is hard to justify two or three years out. So most companies wait. The waiting is what costs them.
None of it is recoverable later. And because a fractional arrangement costs about a third of a fully loaded executive, waiting to avoid that expense usually costs more than the hire would have.
These are the areas market access is responsible for in a launch. I can take on all of them, or only the ones you are not already covering.
Payer value proposition, coverage precedent and utilization management benchmarks, indication sequencing, evidence planning, and the milestone plan from pre-approval engagement through first fill.
Price corridor development, gross-to-net architecture and stress testing, rebate and contracting strategy, government pricing exposure, and pricing governance.
Coding, coverage and payment treated as three separate decisions. Category I and III pathways, Medicare contractor coverage, site-of-care economics, and products with no established benefit category.
Specialty pharmacy and distribution network design, buy-and-bill, patient support hub build and vendor selection, affordability programs, and provider reimbursement support.
Standing up the market access function: role definition and hiring profiles, vendor selection and oversight, board and executive reporting, and handover to the permanent hire.
Primary research with current medical and pharmacy directors, competitive market access monitoring, and reimbursement training for field and commercial teams.
A fixed-scope review of your pricing assumptions, likely coverage, and evidence gaps — ending in a ranked list of what could go wrong and a ninety-day plan. Most engagements begin here.
I hold the market access seat: strategy, payer and pricing decisions, vendor oversight, and reporting into whoever owns commercialization or market access.
Near-full-time coverage of an open market access role through a launch, until the permanent hire is in place.
Pharmacy benefit, medical benefit, and the channel underneath both. Most market access careers cover one of the three.
Four ultra-orphan therapies, two of them priced among the highest in the U.S. market — no comparator and no precedent to lean on.
New-to-market launches across five therapeutic areas, three of which reached blockbuster status. Oral and infused, both benefits.
Ophthalmic and combination products, plus pre-approval market access strategy for a Class I Software as a Medical Device.
First-ever patient support hubs built at two manufacturers, alongside specialty pharmacy and direct distribution networks.
More than twenty-five years across large pharmaceutical, biotech and medical device manufacturers — entirely on the manufacturer side. I have owned this strategy from inside companies rather than advising on it from outside, so what I recommend is something a company can actually approve, fund and execute.
Launch figures reflect products supported in senior market access roles at pharmaceutical, biotech and medical device manufacturers.
If a product is approaching launch and market access needs an owner, I am glad to talk it through.
Bill Engro, Founder & Principal