In today's life sciences market, scientific innovation alone doesn't guarantee success. Your asset may be best-in-class, but if Medical Affairs, Commercial, and Market Access teams aren't telling a unified story, you risk confusion in the field, credibility gaps with stakeholders, and lost ground to faster-moving competitors.
When messaging breaks down, it's not just sales that suffer—trust erodes, HCPs disengage, payers look to the competitor, and patients who need your treatment may never hear about it in time.
At BGB, we've propelled over 50+ launches across 20+ therapeutic categories. We've seen what works—and what doesn't. This quick guide unpacks 5 of the most common scientific messaging pitfalls and how to avoid them. Each one underscores a larger truth: today's launches demand speed, precision, and alignment across science and strategy.
When Medical and Commercial don't speak the same language, the message breaks down
You've got the topline data. The clinical endpoints are strong. But when Medical Affairs builds one version of the story and Commercial builds another, what reaches the field is a blended message that's often incoherent, and sometimes contradictory.
What's really happening?
Internal functions are interpreting data through different lenses:
If everything is important, nothing is memorable
You've got 60 pages of clinical trial results, biomarker data, subgroup analyses, and exploratory endpoints—and every stakeholder wants their piece included.
What's really happening?
In an effort to "cover all the bases," teams overwhelm target customers with undifferentiated facts.
The Result:
HCPs glaze over key information. Payers miss the value signal. Your reps spend more time explaining charts than selling.
Your audience isn't monolithic—your messaging shouldn't be either
You've built a single beautiful, consistent, and clear brand story—and now it's being used across every audience: KOLs, payers, HCPs, nurses, patients.
Clinical trial data gets you noticed.
Real-world evidence earns you belief
You've just secured FDA approval. You've got pristine trial data. But when it comes time to engage skeptical HCPs, their first real question is, "Will this work across the patient populations I see in my practice?" Back in 2018, the FDA began to align on how to evaluate the potential use of real-world evidence to help support approvals.
What's really happening?
You've optimized everything for regulatory success—but not yet for the clinical day-to-day. That gap between the controlled world of the trial and the variability of real-world practice becomes a messaging void.
The Result:
Providers hesitate to prescribe. Access stalls. And the field is stuck relying on anecdotes instead of structured evidence.
If your brand sounds like everyone else, it becomes invisible
You're entering a therapeutic category with 6 other players—2 with similar mechanisms. Your MOA is innovative. Your endpoints are solid. But your messaging sounds… like you've heard it before.
What do all 5 pitfalls have in common? They're not caused by weak science—they're caused by disconnected systems.
Solving these problems requires more than stronger content; it requires a connected messaging ecosystem and a strategic partner who understands how to build one.
Contact Amanda Eckel at aeckel@outreach.bgbgroup.com
© 2025 BGB Group. All rights reserved.