Attendee Profiles
ACRP 2025 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.
By Role
By Practice Setting
Site Includes: Academic Medical Center/University; Clinical Study Site; Healthcare Organization/Association; Hospital; Private Medical Practice; Site Management Organization (SMO); Phase I Unit; Private Practice (Office- or Hospital-Based)
Sponsor Includes: Medical Device Company; Pharmaceutical/Biotech Company
Other Includes: Government Agency (NIH, NHS, NCI, etc.); Regulatory Agency (FDA, EMA, etc.); Training Organization; Staff Recruitment Company; Patient Recruitment Company; Institutional Review Board/Ethics Committee
Upper Management Roles Include: Billing Compliance Officer; Business Development; Director or Manager of Clinical Trial Operations; Director or Manager of Regulatory Affairs; Director of Scientific Affairs; Drug Safety Physician; Executive; Executive Management; Financial Analyst; Investigator; Medical Director; Medical Safety Officer
Support Staff Roles Include: 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
By Experience
By Focus Area
Attendee profiles based on ACRP 2025 participation demographic data.