Steps for a Successful Study Startup
Study startup is a critical stage in a clinical trial to get the study up and running. Efficient study startup lays an important foundation for the trial’s overall success.
Simple Ways to Uncover Research Compliance Blind Spots
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Clinical Research Staffing Contact Request
Engage seasoned research professionals to fill short- and long-term core team roles both on-site and remotely.
Payments Demo Request
Streamline participant payments with automated workflows that simplify stipends, reimbursements, and tracking for coordinators, participants, and finance teams.
OnCore Demo Request
Discover a research management system that unifies protocols, participant data, and financial processes while ensuring billing compliance.
Insights Demo Request
Unlock actionable research analytics with Insights—turnkey dashboards offering clarity on accrual, timelines, and portfolio performance.
EVAL Demo Request
Demonstrate research ROI with EVAL, a tool designed for streamlined reporting and impactful insights for cancer centers and academic institutions.
eReg Demo Request
Streamline regulatory workflows with eReg, a system for managing protocol documents, e-signatures, and seamless sponsor collaboration.
eSource + EDC Demo Request
Simplify data management with eSource + EDC, featuring secure audit trails, calendar building, and seamless CTMS and EMR integration.
eConsent Demo Request
Enhance consenting with eConsent—streamlined workflows, remote signing, and compliance features to improve study oversight and participant engagement.
Clinical Conductor CTMS Demo Request
Streamline clinical trials with Clinical Conductor CTMS—boost enrollment, enhance communication, and optimize financial and operational efficiency.
CCText Demo Request
Enhance recruitment and retention with CCText—CTMS-integrated two-way texting for streamlined outreach, appointment reminders, and consent scheduling.