Attendee Profiles
Nearly 1,300 clinical research professionals from 415 organizations across the clinical research enterprise convened in Orlando to explore ‘What’s Next’ at ACRP 2026. The participants represent a community of clinical research end users, influencers, and decision makers involved in clinical trial management, study conduct, and business operations and administration.
Attendee Demographics
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Academic Medical Center or University Clinical Study Site; Healthcare Organization or Association; Hospital; Private Medical Practice; Site Management Organization (SMO); Phase I Unit; Private Practice (Office- or Hospital-Based)
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Medical Device Company; Pharmaceutical/Biotech Company
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Government Agency (NIH, NHS, NCI, etc.); Regulatory Agency (FDA, EMA, etc.); Training Organization; Staff Recruitment Company; Patient Recruitment Company; Institutional Review Board/Ethics Committee
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Billing Compliance Officer; Business Development; CTMS Manager; Director or Manager of Clinical Trial Operations; Director or Manager of Regulatory Affairs; Director of Scientific Affairs; Drug Safety Manager; Drug Safety Physician; Executive; Executive Management; Financial Analyst; Investigator; Medical Director; Medical Safety Officer
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Clinical Data Coordinator; Clinical Data Scientist; Clinical Research Coordinator; Clinical Research Nurse; Clinical Research Scientist; Data Manager; Director of Pharmacovigilance; Medical Affairs; Medical Writer; Medical Research Scientist; Monitor or Clinical Research Associate; Patient Recruiter; Pharmacist; Project Manager; Quality Control Specialist; Regulatory Specialist; Research Manager; Research Technician or Assistant; Site Selection and Start Up; Trainer
“It is the conference to engage with clinical research professionals, learn practical approaches that can be implemented in our workflows tomorrow, and hear from industry leaders so we understand where research is headed.”