Coordinate day-to-day operation of research and data collection activities; acts as the primary administrative point of contact for internal research staff and…

Provide administrative, clerical, implementation and/or processing support to the project teams and stakeholders.

_Manages day-to-day project activities, including, but not limited to, study development, REB applications, liaising with community partners, writing reports,…

The position supports the Clinical Study Manager and Clinical Operations by tracking and reporting study metrics as well as by performing in-house office…

Valid driver’s license and passport are required. Assist the clinical study team with the development of clinical protocols, case report forms and clinical…

Depuis ses débuts en 2000, notre entreprise à taille humaine bénéficie d’une solide réputation autant pour la qualité de la recherche effectuée que pour la…

The successful candidate will be primarily responsible for the study coordination activities of the lab’s new and ongoing research studies that will involve…

Assist in design, implementation and coordination of all aspects of data collection, source documentation and CRF transcription as per protocol, SOPs and ICH…

Supervises the conduct of clinical studies: acts as liaison between site personnel and the sponsor; performs monitoring in the field; ensures compliance with…

CRAs are to complete all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.

Working under the direction of the Principal Investigator (PI), the clinical research coordinator is responsible for supporting the successful conduct of…

Reporting to the Principal Investigator (PIs) and under the direction of the Research Manager, Urology Research, The Research Coordinator (non-clinical)…

This role requires previous experience in the coordination and administration of clinical studies (patient contact and informed consent; implements and…

Undergraduate degree in a relevant discipline. Undergraduate degree in a relevant discipline (preferably in Health Sciences). $5,209.17 - $7,485.33 CAD Monthly.

Utilizing existing templates, processes and programs as a guide, he or she will adapt/develop, implement, monitor and be accountable for project protocols,…

In this role, you will work closely with our experienced physiotherapists to conduct research studies, gather data, and contribute to the development of…

Valid driver’s license and passport are required. Assist the clinical study team with the development of clinical protocols, case report forms and clinical…

Perform efficacy and safety test on human volunteers. Help to organize volunteer recruitment for clinical trials and manage testing agenda.

Assist with the design and maintenance of Clinical Outsourcing SOPs/Procedures, activity trackers and tools (budget templates, budget review tools, etc.).

Candidates should have experience in the conduct of Phase II - III clinical trials and former training of ICH-GCP. Job Types: Temporary, Part-time.

In-depth knowledge of the drug development process, clinical development planning, clinical research methodologies and execution, and core regulatory…

Work Experience: Previous experience working in a clinical / healthcare environment, including interaction with patients and clinical personnel (nurses,…

A Bachelor's degree in a health care or other scientific discipline or educational equivalent. Supporting the development of a subject recruitment plan.

CAN/US: Depending on role requirements, specific degree and licensure from designated provincial/state body the location of the clinical site (ex. RN, MLT, etc.…