ONCOLOGY · FOR SITES
Oncology clinical trials require strong operational execution. From feasibility to closeout, sites must manage complex protocols, documentation, participant visits, treatment pathways, safety monitoring, eligibility review, and communication with sponsors and CROs.
BRCR Global provides operational support to help oncology sites perform with consistency, confidence, and compliance.
Our support model is designed to reduce administrative burden, improve site readiness, strengthen communication, and help investigators focus on patient care and protocol oversight.
Feasibility Support
We help evaluate patient population, investigator experience, competing studies, referral pathways, and operational capability before site selection.
Study Start-Up
We support essential document collection, regulatory coordination, activation planning, SIV readiness, and communication with study teams.
Recruitment & Pre-Screening
We develop protocol-specific recruitment plans, support EMR review, coordinate referral outreach, and help build structured pre-screening workflows.
Regulatory Coordination
We support documentation, submissions, site files, sponsor/CRO requests, and compliance-related workflows.
Quality Oversight
We help align processes with GCP, SOPs, protocol requirements, documentation standards, and continuous improvement expectations.
Site Operations
We support visit flow, operational planning, team communication, tracking, and escalation of site-level challenges.
Retention Support
We help sites maintain participant engagement through clear communication, visit reminders, barrier identification, and patient-centered follow-up.
Sponsor/CRO Communication
We facilitate timely updates, operational visibility, recruitment reporting, and issue escalation.
A support structure that helps oncology sites improve execution, reduce burden, and participate more effectively in complex clinical trials.
