Clinical Research Project Assistant (SRI) - Centre for Clinical Trial Support - Regular Full-ti[...]

Sunnybrook; Toronto; On-site; CAD 50,000 - 70,000; Full time

Job summary

Sunnybrook Research Institute cherche un Project Assistant pour assister aux opérations quotidiennes d'un essai clinique réglementé par Santé Canada. Les responsabilités incluent la gestion des bases de données, la préparation des rapports, et le soutien à l'équipe de projet. Nous recherchons une personne organisée, avec un diplôme en sciences de la santé et des compétences en communication, qui peut travailler efficacement en équipe.

Benefits

Pratiques d'emploi accessibles

Engagement envers l'inclusion et la diversité

Qualifications

• Diplôme en Sciences de la santé avec expérience de travail.
• Capacité à communiquer efficacement verbalement et par écrit.
• Connaissance des politiques, directives et réglementations actuelles.

Responsibilities

• Maintenir les bases de données administratives.
• Préparer des rapports pour les réunions.
• Soutenir le gestionnaire de projet avec diverses tâches.

Skills

Interpersonal skills

Communication

Attention to detail

Time management

Knowledge of ICH-GCP guidelines

Teamwork

Education

Bachelor’s degree in Health Sciences or related field

Tools

Electronic Data Capture (EDC) programs

MS Office

Job description

Sunnybrook Research Institute (SRI) is a $100M multidisciplinary research community, fully affiliated with the University of Toronto, and servicing a broad spectrum of research programs and platforms. The Centre for Clinical Trial Support (CCTS) is SRI’s coordinating centre in support of investigator-driven clinical research projects and clinical trials. We are seeking a Project Assistant to support the central daily operations of a multi-centered Health Canada regulated clinical trial.

Summary Of Duties (not All-encompassing)

• Maintain administrative databases
• Prepare reports for meetings
• Create agendas and take minutes for meetings
• Filing of emails and documents electronically
• Complete user acceptance testing of study database
• Query sites on data forms
• Run data reports
• Support data cleaning and analysis
• Support monitoring visits
• Draft and update study templates/documents
• Write newsletters and recruitment update emails
• Track and order investigational product
• Support Project Manager with any other tasks as required
  
  

Qualifications/Skills/Requirements

• Bachelor’s degree in Health Sciences, or related field and work experience
• Excellent interpersonal skills
• Be able to communicate easily and successfully, both verbally and in writing
• Be able to work effectively and independently as part of a team
• Knowledge of current policies, guidelines (ICH-GCP), standards, and applicable regulations in order to ensure own work is in compliance
• Able to meet competing deadlines while paying meticulous attention to detail
• Knowledge of Electronic Data Capture (EDC) programs, preferably REDCap
• Skill using various computer systems and software programs including: database management, word processing, spreadsheet and presentation applications, (MS Office)
  
  

Sunnybrook Research Institute is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). If you require accommodation for disability during any stage of the recruitment process, please indicate this in your cover letter.

Sunnybrook Research Institute is strongly committed to inclusion and diversity within its community and welcomes all applicants including but not limited to: visible minorities, all religions and ethnicities, persons with disabilities, LGBTQ persons, and all others who may contribute to the further diversification of ideas.