At C&R Research, our Project Managers oversee the entire lifecycle of clinical trials, from the initial stages through study close-out and data submission, maintaining consistent management throughout. At each phase, they clearly identify objectives and requirements, translating them into actionable timelines and strategies. By proactively understanding sponsor expectations, regulatory requirements, and institutional conditions, they minimize risks and coordinate seamless communication among all stakeholders. They proactively identify potential bottlenecks or delays throughout the project and operate clinical trials stably based on preemptive response plans and backup scenarios.

Considering the complexity and diversity of clinical trials, we maintain a cross-functional team structure that fosters seamless collaboration among experts in medicine, monitoring, data management, statistics, and quality management. Regular project meetings and workflow reviews among field-specific personnel ensure integrated project execution. Communication with sponsors is centralized through the Project Manager, who oversees all issues and decision-making processes, enabling transparent project operations built on trust with our clients.

C&R Research Clinical Research Associates (CRAs) perform their duties based on extensive hands‑on clinical site experience across diverse therapeutic areas, combined with strong regulatory knowledge. Through close communication with trial institutions, they ensure the smooth execution of key activities such as subject enrollment, data collection, and SAE (Serious Adverse Event) reporting. At study initiation, they assess site readiness, verify the proper implementation of enrollment procedures and protocol requirements, and throughout the trial, play a critical role in maintaining the accuracy and consistency of data.

Each CRA understands the specific characteristics of their assigned sites and the preferences of the investigators, enabling a site-tailored approach that fosters effective collaboration and maintains high overall trial quality. Beyond routine monitoring, they provide multifaceted support, including training, document review, and response to ethical issues, serving as a true operational partner to the trial sites.