The pharmaceutical and life sciences industry is evolving rapidly, but one challenge persists: how to communicate complex science clearly and creatively. In an era of omnichannel communication where patient-centricity is the cornerstone of trust and engagement, pharma companies must go beyond traditional formats to deliver content that resonates with healthcare professionals (HCPs), patients, caregivers, and patient support and advocacy groups.
Moreover, the results of a recent LinkedIn poll that we, Cactus Life Sciences, conducted reveal that 47% of respondents prioritize patient-reported outcomes (PROs) as primary endpoints, and 32% emphasize diversity in clinical trial enrolment. These findings underscore the growing demand for real-world evidence (RWE) and patient-centric approaches in pharma communication.
As a full-service, agile MedComms agency, we believe that innovative communication strategies can transform engagement and position pharma as a trusted partner. Here are four actionable ideas to help pharmaceutical and life sciences organizations lead the way.
1. Storyboards and micro-animations: Real-world evidence (RWE) made simple
Real-world evidence (RWE) is critical for informed decision-making, but dense and lengthy reports often fail to engage busy clinicians. A better approach? For every RWE study, create a single-screen storyboard summarizing:
- Population
- Research question
- Key findings
- Limitations
Pair this with a 20-second animation to visualize the data dynamically. This format makes RWE accessible, shareable, and actionable, perfect for congress booths, HCP portals, and social media. By simplifying evidence without sacrificing rigor, pharma can accelerate adoption and improve clinical impact.
2. HCP-to-patient “pass-along” handouts: Empowering conversations
Patients often leave consultations with unanswered questions about their medical conditions. Pharma can bridge this gap by creating short, quick summaries as communication tools for HCPs to share during appointments, with the aim of improving patient engagement and patient education. For example, plain language summaries (PLSs), patient information leaflets (PILs), clinical study recruitment materials, and risk minimization materials. Each handout or information piece/material should include:
- Condition basics, i.e., disease-state information
- Three to five questions patients can/should ask
- A QR code linking to a patient-friendly information leaflet (PIL/PLS)
This handy tool empowers patients, enhances health literacy, and positions pharma as a partner in patient engagement. Furthermore, in our poll on LinkedIn, 16% of respondents highlighted plain-language material uptake as an important patient-centric metric, reinforcing the need for tools like pass-along handouts to improve patient understanding and health literacy. Scalable across therapeutic areas, these handouts/materials can become a cornerstone of patient-centric communication.
3. Community co-creation workshops: Designing with patients, not just for them
Patient support and advocacy groups offer invaluable insights, yet their input often comes too late. Host quarterly virtual co-creation workshops with support and advocacy representatives to storyboard upcoming patient explainer assets. After each session, publish a summary of what changed based on feedback.
This transparency builds trust and ensures content reflects real-world needs, whether it is simplifying medical jargon or adding culturally relevant examples. Also, another of our recent LinkedIn polls shows that 55% of medicine and life sciences professionals see the biggest shift for Medical Affairs as moving from reactive to strategic engagement, with 36% favoring continuous interaction, thus validating why co-creation workshops are essential for sustained trust and relevance. For pharma, co-creation workshops are not just compliance; they’re a strategic advantage.
4. Layered consent: Making clinical trial participation easier
Informed consent is essential but often overwhelming. Replace lengthy documents with layered consent, which is an interactive process combining:
- Text, visuals, videos, and audio
- Teach-back prompts before proceeding
- Exportable comprehension logs
This approach improves understanding, enhances trust, and supports ethical standards. Studies show that patient-friendly language and layered consent models can boost clinical trial participation and retention, making trials more inclusive and efficient. In addition, when one of our LinkedIn polls asked which trial model people prefer, 56% of respondents favored hybrid models. This is why layered consent becomes even more critical to simplify participation across both digital and site-based touchpoints, ensuring inclusivity and clarity.
Why these innovations matter
These findings and insights underscore a fundamental truth: patient-centricity is the baseline, not the bonus. No one now asks if patient-centricity matters; everyone demands to know how well you deliver it. From prioritizing PROs to embracing hybrid trials and communication strategies that include RWE storyboards, pass-along handouts/information materials, co-creation workshops, and layered consent, the industry is signaling a clear need for communication strategies that combine clarity, collaboration, and compassion. In a world where attention is scarce and data is abundant, pharma must communicate not just what it knows, but what matters.
At Cactus Life Sciences, we champion agile, patient-inclusive communication that combines scientific rigor with human-centered design. By embracing these creative approaches, pharma can strengthen relationships, empower patients, and accelerate the adoption of evidence-based practices.
Final thought
When participation feels easy and information is clear, everyone wins: patients, providers, and pharma alike. Adding patient-friendly language and layered consent can significantly increase trial enrollment while reducing dropout rates. It’s time to make these innovations the norm.
Disclaimer: Generated with Microsoft Copilot under human supervision.

Kwisha Shah
Marketing Content Manager
