Job Title

Global Clinical Trial Manager (Remote Canada)Fully remote, no travel, must be located in Canada. Position filling fast, apply today.Global Clinical Trial Managers are responsible for the planning and execution of trials from the clinical perspective, ensuring they adhere to protocols, regulations, and company standards. Manage the trial from start to finish, overseeing site initiation, monitoring, and close-out, while maintaining site compliance and documentation. Role also involves communication and collaboration with various stakeholders, including sites, vendors, and internal teams.Must currently be working for a CRO, Pharmaceutical or Biotechnology Company, have a bachelors degree with at least 5 years clinical and 3 years of global trial management with a title such as Global Clinical Trial Manager, Global Study Manager, Global Trial LeadKey Responsibilities:Serving as the global primary point of contact for assigned trial sites, developing relationships, and ensuring site readiness for study conduct.Trial Oversight:Contributes and develops to program/study-specific materials e.g., monitoring plan, study specific training documents.Accountable for site-level goal setting and study-specific deliverables for clinical sites within their country/-ies.Contributes to, deliver and/or lead CRA, Investigator and Study Coordinator training.Managing all aspects of trial execution, including site initiation, monitoring, and close-out, while ensuring adherence to protocols, SOPs, and regulations.Documentation and Compliance:Ensuring accurate and complete documentation, including site records and training, and maintaining compliance with GCP, regulations, and company policies.Communication and Collaboration:Maintaining open communication with sites, vendors, and internal teams, including Clinical Trial Leads (CTLs), Clinical Trial Managers (CTMs), and other relevant stakeholders.Quality and Risk Management:Identifying and escalating issues related to quality, timelines, and budget, and ensuring appropriate risk mitigation strategies are in place.Regulatory Compliance:Ensuring clinical trial regulatory strategies align with scientific, therapeutic, and regulatory expertise, and that all applicable regulatory requirements are met.Required Skills and Qualifications:Must currently be working for a CRO, Pharmaceutical or Biotechnology Company, have a bachelors degree with at least 5 years clinical and 3 years of global trial management with a title such as Global Clinical Trial Manager, Global Study Manager, Global Trial LeadEducation: Bachelor's degreeExperience: Strong understanding of GCP, relevant regulations, and clinical trial processes.Skills: Excellent communication, organizational, problem-solving, and leadership skills