3 Keys to Building a Top-Notch Clinical Trial Staff

Staffing issues are top of mind among leadership at clinical research organizations around the world. Look no further than the ongoing bidding war for monitors/CRAs at sponsors and CROs for proof that top-quality clinical trials staff are a hot commodity. Building a high-quality staff at any clinical research organization – be it a sponsor, CRO, […]

Rookie Investigators Underestimate Seriousness of Signing FDA 1572s

Too many green principal investigators (PIs) blithely sign the U.S. Food and Drug Administration (FDA)-demanded Statement of Investigator (Form 1572) and run the risk of falling into serious trial deviations or even potential legal issues, warns Randall Stoltz, medical director with the Covance Clinical Research Unit in Evansville, Ind. “You have to ask what you […]

CISCRP, ACRP Collaborate on 5k Run & Walk Event to Recognize All Clinical Trial Volunteers

FOR IMMEDIATE RELEASE: February 2, 2016 CONTACT: Jeremy Glunt + 1.703.258.3506 media@acrpnet.org

Research Professionals and the Public to Honor Study Volunteers Who Give the Gift of Participation in Clinical Research

Washington, DC and Boston, MA – The Association of Clinical Research Professionals (ACRP) and the Center for Information and Study on Clinical Research Participation (CISCRP), two […]