Dedicated exclusively to clinical research, Diex Research is a thriving company with international experience.
Sherbrooke, Québec
Dedicated exclusively to clinical research, Diex Research is a thriving company with international experience that provides a unique business model and an opportunity for private partnership with pharmaceutical and biotechnology industries. Backed by a team of practiced professionals and espousing a winning blend of quality care and scientific rigour, Diex Research conducts phase I to IV clinical studies designed to satisfy client demands in full, while complying with all applicable standards and regulations along with adjusting to specific needs of the clients or of the industry. Dedicated to excellence and sustained improvement, Diex Research is committed to establishing a solid partnership with its clients. This is achieved through careful listening, an active approach and a constant desire to adapt, and ultimately ensures project completion and customer satisfaction.
On-site
The incumbent will support the clinical team during participant stays by performing medical monitoring, collecting study data, and administering medication according to research protocols. They will also assist the research coordinator and ensure all study procedures are followed accurately.
On-site · Sherbrooke
Explain clinical studies and obtain participant consent, provide medical follow-up in accordance with research protocols, and collect study data through assessments such as questionnaires, vital signs, blood tests, and ECGs. Explain and administer study medication, monitor adverse effects, support the research coordinator, and assist with participant recruitment and data entry as needed.
On-site · Québec
Explain clinical studies and obtain participant consent, provide medical follow-up in accordance with research protocols, and collect study data through questionnaires, vital signs, blood draws, and ECGs. Explain and administer study medication, monitor adverse effects, support the research coordinator, and assist with participant recruitment and data entry as needed.
On-site · Joliette
Coordinate and plan the implementation of approximately ten clinical research protocols while ensuring legal and regulatory compliance and protecting patients’ rights and welfare. Train and support team members, coordinate recruitment and marketing activities, attend study training and monitoring visits, and collect clinical data through assessments and procedures as applicable.
