?? Honoring the Women Who Power Clinical Research ?? #WomensHistoryMonth | #ClinicalResearch | #DEI It’s a challenging time for DEI in many industries, including ours. But this Women’s History Month, I want to take a moment to celebrate the incredible women—past and present—who have shaped the field of clinical research. When we talk about women in clinical trials, we often focus on representation in study populations—and that’s absolutely critical. But just as important are the women behind the trials. The ones designing protocols, coordinating sites, managing data, leading operations, mentoring teams, and advocating for ethical, inclusive science. The clinical research industry runs on the hard work, dedication, and brilliance of women at every level—and often, their contributions go unrecognized. As a woman working in this field, I see our role as more than just a job title. We are innovators, problem-solvers, patient advocates, and collaborators. We’re also mentors, supporters, and sometimes the steady hands holding things together when studies stall or timelines shift. So how do we keep moving forward—together? ?? We lead with integrity and courage. ?? We lift each other up—formally and informally. ?? We stay committed to equity, even when it’s hard. ?? And we make space for the next generation of women who will take this industry to even greater heights. To every woman working in clinical research: thank you. Your voice matters. Your work matters. And you’re helping shape a better, more inclusive future for science and for patients. Let’s keep going. ?? #WomenInSTEM #ClinicalTrials #WomenInResearch #Leadership #Mentorship #InclusionMatters #CelebrateWomen
Florence Healthcare
软件开发
Atlanta,Georgia 20,725 位关注者
Connecting Clinical Trial Workflows, powered by Site Enablement
关于我们
Florence Healthcare is the leading provider of the Site Enablement Platform, committed to accelerating cures by better connecting sponsors, CROs, and research sites. The company's integrated platform streamlines the clinical trial process, enabling seamless collaboration and more efficient management of clinical research workflows. Florence Healthcare is dedicated to fostering innovation and improving patient outcomes worldwide with over 12,000 connected research sites on its platform in 45 countries, facilitating more than 6.5 million research workflows every month.
- 网站
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https://www.florencehc.com
Florence Healthcare的外部链接
- 所属行业
- 软件开发
- 规模
- 201-500 人
- 总部
- Atlanta,Georgia
- 类型
- 私人持股
- 创立
- 2014
- 领域
- Clinical Trials、Electronic Trial Master File (eTMF)、Clinical Trial Sites、Clinical Trial Management、21 CFR Part II、eRegulatory、eSource、Remote Monitoring、Cancer Centers、Academic Medical Centers、CROs、Pharmaceuticals、Medical Device、Coordinating Centers、Electronic Regulatory、Electronic Signature、Document Management、Clinical Research、Software和Data Management
地点
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主要
600 Peachtree St NE
Suite 920
US,Georgia,Atlanta,30308
Florence Healthcare员工
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Ryan Jones
Cofounder and CEO, Florence Healthcare
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Christina Ortega
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Gia Ganesh, MIS, MBA, SHRM-CP
Scaling People and Culture at Startups | Building high performance , high growth and Inclusive cultures | Employee Experience Builder | People First…
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Andres Garcia
Co-founder and CTO at Florence Healthcare | Endeavor Entrepreneur
动态
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?? Last chance to register! ?? Join us tomorrow at 11 AM ET for an exclusive webinar exploring how top clinical research sites are modernizing their eISF systems to save time, reduce compliance risks, and operate more efficiently. Whether you're working with outdated technology, still relying on paper-based processes, or just curious about what a modern eISF could look like — this session is for you. We’ll cover: ? Current trends driving eISF innovation ? Must-have features top research sites now expect ? A live demonstration of tools like DOA Logs, Document Redaction, Secure Monitor Access, Study Binder Management, Granular Access Controls, and more ? Proven strategies for transitioning from paper or legacy eISF systems with minimal disruption Register: https://hubs.li/Q03d8slZ0
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Our second Women’s History Month spotlight: Henrietta Lacks. She never consented to being part of medical history—but her HeLa cells transformed it. Her story is a powerful reminder of the need for ethical research practices and equitable representation in clinical trials. We honor her legacy by advocating for greater transparency, respect, and inclusivity in research—because medical progress should never come at the cost of consent or fairness. #WomensHistoryMonth #WomeninClinicalResearch #WomeninScience
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The future of clinical trial success starts with the site experience. Join us on Thursday, April 3 at 11 AM EST for a live webinar: How Sponsors & CROs are Investing in Site-Facing Capabilities for Clinical Trials Today Why should you attend? ? Stay ahead of industry trends: Learn how sponsors are reshaping their operations by prioritizing site-facing technology in 2025. ? Get real-world insights: We’ll walk through an actual templated RFP and case studies from sponsors who have successfully optimized site operations. ? Enhance operational efficiency: Discover key platform capabilities that accelerate study startups, improve site qualification, and streamline patient enrollment. ? Gain a competitive edge: Learn practical strategies to mitigate risk, scale workforce capacity, and boost trial performance. Save your spot now: https://hubs.li/Q03cK63m0
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The Navigating Canadian eRegulations and Clinical Trials Landscape webinar was packed with insights, challenges, and solutions for compliance and operational efficiency in Canada. If you missed it, here’s a quick recap of what you need to know ?? Top Takeaways from Our Experts: ? Canada ranks 11th globally in clinical trial activity, with over 3,500 ongoing studies. But patient recruitment bottlenecks and regulatory hurdles are slowing Canada down. ? The Can-Review initiative is a game-changer moving towards a single national ethics review process with clear timelines to make Canada one of the fastest countries for clinical trial approvals. ? Technology adoption is no longer optional—eConsent, remote monitoring, and automated workflows are key to compliance and efficiency in clinical trials. ? Privacy laws like Quebec’s Law 25 and Alberta’s PIPA updates are reshaping how we handle participant data. Compliance isn’t just about avoiding fines—it’s about trust.” – Sara Saunders we truly want to accelerate research, we need to digitize, streamline site approvals, and embrace harmonization. Let’s not hold ourselves back.” – Catherine Gregor Why This Matters: ? Canada is making major regulatory shifts to align with global standards ? A 30-day trial approval goal is on the horizon with Can-Review ? eRegulatory adoption is critical to faster, more efficient clinical trials Watch the full webinar to dive deeper into these critical updates → https://hubs.li/Q03ckcR90
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Did you know that one of the earliest pioneers of modern clinical research was a woman? This Women’s History Month, we’re celebrating the trailblazing women who shaped clinical research, starting with Dr. Janet Lane-Claypon. In the early 1900s, she conducted the first-ever case-control study on breast cancer, laying the foundation for evidence-based medicine. Her groundbreaking work continues to influence how we approach clinical research today. Despite these contributions, women remain underrepresented in studies that directly impact their health. Her legacy is a powerful reminder: diverse participation in clinical trials isn’t just important—it’s essential. #WomensHistoryMonth #ClinicalResearch #ClinicalTrials
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Is your eISF keeping up with your research needs? As workflows evolve, research sites, hospitals, and health systems are upgrading their eISF solutions—without downtime or disruption. Join us on Tuesday, March 25 at 11 AM ET to learn: ? The latest innovations in eISF/eReg technology ? A step-by-step migration process used by leading research sites ? How to avoid hidden costs and compliance risks ? A live demo of Florence’s eISF, trusted by 30,000+ research sites Register now: https://hubs.li/Q03bL9fB0
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Did you catch the December Journal of Clinical Oncology? Florence remains the top eRegulatory platform for North American Cancer Centers! Even more exciting? 78% of Cancer Centers now use an eReg solution—a testament to the growing need for automation in clinical research. Our mission is to empower research sites with the best technology to streamline workflows and foster seamless collaboration across the research community. Here’s to advancing cancer research together! Read the journal: https://hubs.li/Q039pCnN0
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