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Research Project Manager I

Hamilton, ON
  • Nombre de poste(s) à combler : 1

  • 41.64 à 53.38 $ selon l'expérience
  • Temps plein
  • Date d'entrée en fonction : 1 poste à combler dès que possible

The Research Project Manager I purpose is to lead a team in the central coordination of one or more multi-center research studies. They would ensure relevant clinical and research methodology is applied throughout the conduct of the research study. Accountabilities include: Development and monitoring of study timelines and key deliverables in collaboration with internal and external stakeholders and project team members; Provide coordination and direction in the development of data management methodologies for multiple studies; including key data management methods such as; data collection, entry, verification, data validation, quality control, adjudication tracking and event reporting for large clinical datasets; Data management: Evaluate and review high level study reports for compliance, safety and central monitoring for the duration of the trial and manage communication of inconsistencies with program manager, principal investigator, steering committee(s), and data/trial monitoring committee; Site Management: Develop investigator training procedures and provide investigator site training to participating centres and external stakeholders (contract research organizations, research and core laboratories); Staff supervision and training; Grant and financial planning with development and support of research budgets; Regulatory, documentation, and research practices


Qualifications

1. Undergraduate degree in sciences or health science 
2. A clinical research certification (CCRP, ACRP or post-graduate certification in clinical research) is preferred
3. Minimum of 3 years’ experience in multi-centre research studies and the management of large clinical research datasets
4. 3  years' of working knowledge of PHRI systems, processes, organizational structure and SOPs
5. 3  years supervisory experience and team coordination experience
6. Excellent communication, problem solving skills and ability to work flexible hours
7. Knowledge of ICH-GCP Guidelines and international research requirements
8. Broad knowledge of research methodology, clinical trials and drug development processes


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