Consulting Services


Our Services

Performance of pre-study, initiation, interim monitoring and close-out visits from phase I - IV for clinical sites located mainly in Canada. Assisting in Study start-up (site identification, elaboration of study tools/forms such as informed consent form, case report form template)
Liaison between the Investigational sites (site management) or vendors (e.g., management of contracted Clinical research organizations) and the Sponsor.
Track clinical study performance to ensure on-time delivery, within scope and budget. Proactively organizing and tracking all study activities, milestones, and metrics using Clinical Trial Management Systems (CTMS).
Patient recruitment (identifies and screens potential subjects); plan, implement, review and coordinate all aspects of data collection and source documentation. Coordinate patient visits and schedule as per study protocol.

ABOUT USSonia Delva R.N., B,Sc.

I am the Founder of Delva Consulting Inc. with more than 20 years experience in the Clinical Research field. I am bilingual in French and English and hold a B.Sc. In Nursing Sciences from Université de Montréal and am certified in ICH-GCP regulations. My expertise in clinical research was developed from many years of hands-on experience across several therapeutic areas (Clinician Nurse, Clinical Research Associate (CRA), Project Manager, Study Manager and Clinical research coordinator).