Clinical Project Management

At MedQualis your clinical trial gets the drive, attention, and devotion it deserves. We work for you and with you in the achievement of a successful study.
Your project manager is a single point of contact, allowing fast, efficient action and ensuring quick dissemination of information. Your Project Manager is responsible for anticipating and removing roadblocks, for maintaining project requirements, for controlling costs, for efficient patient recruitment, and for performance.

Clinical Research Associate / Monitoring

At MedQualis, our trial monitors oversee all aspects of a study, ensuring rigorous compliance with protocol, quality standards, data collection, and regulatory requirements. Our monitors (CRAs) are dedicated to building productive working relationships with our clients, investigators, and study coordinators. We adhere strictly to FDA/TPD regulation and to the International Conference on Harmonization/World Health Organization Good Clinical Practice standards (ICH/GCP).

Our monitors have experience in conducting site evaluation visits, site initiation visits, periodic monitoring visits, and study termination visits as well as all in-house monitoring functions, including adverse events reporting.

At MedQualis we offer an experienced team with strong and diversified scientific backgrounds.