ACRP 2020 participants represent a diverse community of professionals involved in clinical trial management, study conduct, and business operations and administration.
Connecting upper management and support staff from sites, sponsors, CROs and more, ACRP 2020 is where professionals focused on improving clinical trial leadership and execution make a difference.
Attendees by Role
Upper Management Roles Include: Business Development; Director or Manager of Clinical Trial Operations; Director or Manager of Regulatory Affairs; Drug Safety Physician; Executive; Executive Management; Financial Analyst; Investigator; Medical Director
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; Monitor or Clinical Research Associate; Pharmacist; Project Manager; Quality Control Specialist; Regulatory Specialist; Research Manager; Research Technician or Assistant; Site Selection and Start Up; Trainer
Attendees by Practice Setting
Site Includes: Academic Medical Center/University; Hospital; Clinical Study Site; Private Medical Practice; Site Management Organization (SMO); Clinical Study Site; Phase I Unit; Private Practice (Office- or Hospital-Based)
Sponsor & CRO Includes: Contract Research Organization (CRO); Medical Device Company; Pharmaceutical/Biotech Company
Other Includes: Healthcare Organization/Association; Government Agency (NIH, NHS, NCI, etc.); Training Organization; Staff Recruitment Company; Patient Recruitment Company; Institutional Review Board/Ethics Committee
Attendees by Experience
Attendees by Focus Area
Attendee profiles based on ACRP 2019 participation demographic data.