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How Social Media for Life Sciences Is Reshaping Clinical Trials

Life Sciences & Healthcare

Last Updated: November 26, 2025

In 1943, the first modern clinical trial for common cold treatment was conducted in Great Britain. Over 1,000 patients from across the nation participated in this double-blinded trial, traveling an average of two to three hours by train or car to reach a single, centralized clinical trial location. The clinical investigators wrote the observations by hand, and it took 18 months to synthesize the results and generate a report. Looking back at this trial from a 21st-century perspective, it appears archaic: patients had to go to great lengths to participate, had little visibility into the trial results, and received minimal access to their own clinical trial data. Meanwhile, clinical investigators relied on a limited set of diagnostic tools and paper-based recording devices.

Fast forward to today, the landscape of clinical trials has undergone a dramatic transformation. Social media for life sciences has emerged as a powerful tool for pharmaceutical companies and Contract Research Organizations (CROs), reshaping clinical trials into faster, more inclusive, and patient-centered experiences.

This blog explores how integrating social platforms with decentralized clinical trial (DCT) strategies is revolutionizing the clinical research landscape, empowering organizations to stay ahead in the race for innovation.

Why Social Media Is a Game-Changer for Clinical Trials 

The pandemic fast-tracked digital transformation within the life sciences sector, with clinical trials showcasing the most prominent advancements. One such advancement was the rise of decentralized clinical trials (DCTs), which highlighted the need for flexible and accessible trial designs, ultimately enhancing patient engagement and data collection efficiency.

What are decentralized clinical trials?

Decentralized clinical trials are a modern approach to clinical research that allows for the execution of trial protocols outside of traditional centralized locations, such as hospitals or research centers.

According to the FDA, DCTs utilize telemedicine and local healthcare providers, enabling patients to participate from their homes through telehealth visits and familiar technologies like smartphones and wearables. This model eliminates the need for patients to travel repeatedly to a central site for enrollment, consent, data collection, or symptom monitoring. DCTs can be fully decentralized, where all aspects of the trial are conducted remotely, or hybrid, incorporating both virtual and in-person elements.

DCTs + Social Media = The Future of Clinical Research

Social media platforms are driving real impact across the clinical trial lifecycle as follows:

  • Faster Recruitment: Social campaigns reduce enrollment timelines by up to 70% compared to traditional outreach.
  • Broader Reach: Platforms like Facebook and Instagram connect researchers with underrepresented and rural populations.
  • Better Patient Experience: Real-time, two-way communication builds trust and improves trial retention.
  • Lower Costs: Paid social is more efficient than print or television for reaching targeted demographics.

While decentralized clinical trials allow patients to participate from home or nearby locations. When the reach of social media is combined with DCTs, it breaks down participation barriers and ensures diversity at scale. This integrated model has created new avenues for patient engagement, allowing participants to join trials from their homes and reducing the logistical barriers typically associated with traditional trial model

Leading pharma companies like Pfizer and Novartis are leveraging this blended approach to educate patients, recruit them, gather feedback, and build trust. Meanwhile, CROs are embracing these strategies by launching targeted campaigns aimed at specific patient populations. This approach enhances enrollment timelines and helps reduce recruitment costs significantly.

Benefits of this blended approach include:

  • Pre-screening through interactive campaigns
  • Digital outreach for rare and hard-to-reach conditions
  • Real-time updates to improve compliance and retention
  • Education and engagement via patient advocacy partnerships

The result? A more connected, inclusive, and transparent trial experience.

Real-Life Examples of Social Media Transforming Clinical Trials

Here are three real-life examples of CROs and life sciences organizations effectively using social media to enhance clinical trials:

  1. Biogen Idec and MyHealthTeams Partnership
    Biogen Idec partnered with MyHealthTeams, a social network platform for patients with chronic conditions, to recruit participants for clinical trials. This collaboration significantly accelerated recruitment for multiple sclerosis trials, increasing the screening rate from 6 patients per week to 400 patients per week. This demonstrates how leveraging patient advocacy groups and social networks can drastically improve recruitment efficiency.
  2. #WhyWeDoResearch Campaign
    This Twitter campaign, initially aimed at raising awareness about research among healthcare professionals, patients, and the public, quickly gained traction. Within five months, it reached 14 countries and engaged over 2,300 participants. The campaign now includes opportunities for patients to participate in clinical studies, showcasing how social media can foster global engagement in research.
  3. Brown-Lifespan Center for Digital Health
    The Brown-Lifespan Center for Digital Health has been actively using social media to recruit participants for various studies. For example, they used Twitter and Facebook physician groups to recruit doctors for qualitative interviews on telehealth in older adults. This demonstrates how social media can also be used to engage healthcare professionals in clinical research.

How Hexaware Supports Digitally Enabled Trials

At Hexaware, we’ve built an AI-powered patient engagement platform that integrates clinical trial operations with social media insights, omnichannel communication, and real-time analytics.

Key capabilities include:

  • 360° patient profiles for personalized care
  • Seamless integration with Health Cloud and eTMF systems
  • Cohort-based risk stratification
  • Transparent, real-time reporting for sponsors and CROs

Customer Success Story:

We partnered with the world’s largest CRO to develop an innovative, agile virtual trial platform, designed for scalability, speed, and patient-centricity. Our collaboration has led to remarkable outcomes:

  • 2x Faster Subject Recruitment Reporting: Accelerating the recruitment process to bring trials to fruition more quickly.
  • 25% Increase in Patient Onboarding Rates: Enhancing patient acquisition through targeted outreach.
  • 80% Improvement in Efficiency and Documentation Accuracy: Streamlining operations for greater reliability and compliance.

Read the full case study here.

The Bottom Line

Social media and decentralized trials aren’t just tools—they’re strategic imperatives for modern clinical research. The organizations that embrace digital-first patient engagement are gaining real advantages in trial speed, diversity, and cost efficiency.

Ready to rethink your clinical trial strategy?
 Let’s co-create the next generation of connected, inclusive, and outcomes-driven research. Contact us at marketing@hexaware.com to get started.

About the Author

Venkata Suresh Babu Bondu

Venkata Suresh Babu Bondu

Venkata is a proven expert in the life sciences domain with 25 years of experience driving digital innovation across drug research, development, manufacturing, and clinical study operations. Specializing in AI-powered transformation and advanced analytics, he delivers impactful solutions across the value chain. As a visionary leader, Venkata builds and leads diverse, high-performing teams that consistently achieve operational excellence. His ability to align digital strategies with business goals makes him a trusted innovator and leader in the life sciences industry. He has held key roles at IQVIA and Saama Technologies, contributing to the development of cutting-edge digital and data science solutions in clinical research and pharma manufacturing.

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FAQs

Social media for life sciences improves patient recruitment as follows:

  • It targets specific demographics by leveraging platforms like Facebook and Instagram, allowing researchers to reach individuals based on location, age, health interests, and more.
  • Increases awareness and accessibility through engaging content such as short-form videos and autonomy-supportive messaging, which improves attitudes toward participation.
  • Reduces recruitment delays by streamlining outreach and enabling predictive enrollment timelines

DCTs differ from traditional trials in several ways as follows:

  • Technology use: DCTs leverage telemedicine, wearable devices, and electronic data capture systems for remote monitoring and data collection.
  • Location: Traditional trials require in-person visits to clinical sites, while DCTs allow participants to engage from home or local healthcare facilities.
  • Accessibility: DCTs reduce geographical and logistical barriers, improving diversity and inclusion in participant pools.

Integrating social media with decentralized clinical trials offers several advantages:

  • Expanded reach: Social media helps DCTs connect with diverse and geographically dispersed populations.
  • Improved recruitment and retention: Targeted campaigns and community engagement foster trust and encourage participation.
  • Enhanced patient experience: Combining digital outreach with remote trial models creates a more convenient and patient-centric approach.

Social media campaigns support retention by:

  • Maintaining ongoing communication with participants through updates, reminders, and educational content.
  • Fostering community and support via online groups and forums that help participants feel connected and valued.
  • Reducing dropout rates by addressing concerns and providing real-time assistance through interactive platforms.

Researchers maintain participant engagement as follows:

  • Personalized communication tailored to participant preferences and needs.
  • Continuous support through helplines, digital tools, and patient navigators.
  • Flexible protocols that accommodate participants’ schedules and reduce burden.
  • Incentives and recognition to acknowledge participant contributions and encourage continued involvement.

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