Welcome to Conduct Research, a renowned and trusted Site Management Organization (SMO) located in the dynamic and thriving city of Edmonton, Canada. Our organization is dedicated to delivering excellence in clinical trial site management, offering comprehensive services to a diverse range of clients including pharmaceutical companies, contract research organizations (CROs), and academic institutions.

As a leading SMO, we offer a comprehensive range of services designed to streamline the site management process and optimize study outcomes. From site identification and selection to site initiation and activation, our team handles every aspect of site management with meticulous attention to detail. We believe that well-trained site personnel are essential for the smooth and efficient execution of clinical trials. Therefore, we provide customized training programs to enhance their knowledge and skills, ensuring adherence to study protocols and regulatory guidelines.

We understand that successful clinical trials rely on effective patient recruitment and retention. To address this crucial aspect, we employ targeted strategies and patient-centric approaches to identify and engage potential participants, ultimately maximizing enrollment and minimizing dropouts. Our dedication to maintaining the highest standards of data integrity is reflected in our robust data management and quality assurance practices. We employ robust systems and processes to ensure secure and accurate data collection, storage, and analysis. This allows us to provide our clients with comprehensive reports and real-time access to study data, enabling informed decision-making throughout the trial.

At Conduct Research, we firmly believe in the power of collaboration and open communication. We forge strong partnerships with our clients, working closely with them to understand their unique needs and goals. Our flexible approach allows us to tailor our services to meet the specific requirements of each project, ensuring that we deliver customized solutions that align with study timelines and budgetary constraints.

At Conduct Research, we place patients at the center of everything we do. We are committed to a patient-centric approach that emphasizes their well-being, safety, and involvement throughout the trial process. We recognize the importance of clear and transparent communication, respect for patient rights, and ethical treatment. By fostering trust, engagement, and collaboration with study participants, we aim to create a positive experience that supports successful patient recruitment, retention, and overall trial success.