Santé Québec - Centre hospitalier universitaire Sainte-Justine. Le plus grand centre mère-enfant au Canada
Montréal, Québec
Le Centre hospitalier universitaire Sainte-Justine est le plus grand centre mère-enfant au Canada et l'un des quatre plus importants centres pédiatriques en Amérique. Ses 5 000 employés et ses 500 médecins, dentistes et pharmaciens oeuvrent dans un milieu à la fois hautement innovant, où des connaissances sont générées et partagées au quotidien, et respectueux des personnes, plaçant le patient et sa famille au coeur de la pratique. Associé à l'Université de Montréal, le CHU Sainte-Justine est de loin le plus grand centre de formation en pédiatrie au Québec et un chef de file au Canada; il accueille chaque année plus de 4 000 étudiants et stagiaires.
On-site · Montréal
Coordinate the planning, execution, and oversight of Phase I clinical research projects, including multicenter study operations, protocol and document development, ethics submissions, recruitment, budgets, and site agreements. Maintain complete regulatory files in accordance with Good Clinical Practice and coordinate research data collection, quality monitoring, and safety oversight.
On-site · Montréal
Plan, carry out, and monitor pediatric clinical research protocols, including recruiting and consenting participants, providing clinical follow-up and education, administering investigational medications, and performing protocol-required tests. Collect and enter study data, resolve queries, support monitoring visits, and handle and ship clinical samples while following applicable regulations and study requirements.
On-site · Montréal
Recruit and consent research participants, provide protocol-based clinical follow-up and education, administer investigational medications, and coordinate protocol-required tests. Collect and enter study data, resolve data queries, support monitoring visits, and handle clinical samples while ensuring research protocols and applicable regulations are followed.
On-site · Montréal
Coordinate and carry out clinical research protocols, including recruiting participants, obtaining consent, providing clinical follow-up and education, administering investigational medications, and performing protocol-required tests. Collect and enter study data, resolve queries, support monitoring visits, handle and ship clinical samples, and complete required project and safety training.
On-site · Montréal
Recruit and consent research participants, provide protocol-based clinical follow-up and education, administer investigational medications, and coordinate protocol-required tests. Collect and enter study data, resolve data queries, support monitoring visits, and handle clinical samples in accordance with applicable research requirements.