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Clinical Trials Project Coordinator
3 months ago
This role is integral to the Non-Academic Staff Association (NASA) and operates in a hybrid model, combining remote work with in-person responsibilities.
About the University of Alberta:
The University of Alberta is situated on Treaty 6 territory and honors the diverse histories, languages, and cultures of First Nations, Metis, Inuit, and all First Peoples of Canada, whose contributions continue to enrich our community.
As a vibrant hub of knowledge, the University is home to over 14,000 faculty and staff, more than 40,000 students, and a global alumni network of 300,000.
Key Responsibilities:
- Collaborate with the Director of Operations of the Clinical Trials Office (CTO) to design, implement, manage, and assess research and administrative strategies crucial for the effective execution of clinical trial projects.
- Provide leadership to the project team, overseeing the overall operation, coordination, and management of clinical projects while serving as the primary liaison with external partners.
- Co-develop and facilitate CANTRAIN educational, experiential, and mentorship programs, alongside capacity-building initiatives for the CANTRAIN clinical research training platform across various sites.
- Plan and deliver CANTRAIN clinical trial training programs and capacity-building initiatives targeted at frontline learners and practitioners (50%).
- Create educational content and capacity-building programs that incorporate CANTRAIN's educational, experiential, and mentorship activities.
- Engage in the Knowledge Management Strategy at CANTRAIN, focusing on mobilization and translation.
- In collaboration with the CTO Director of Operations, identify, evaluate, and recruit research sites, ensuring alignment with protocol requirements and conducting feasibility analyses for successful project completion.
- Organize and execute investigator meetings, developing and presenting project-specific materials to enhance communication among study team members and site personnel.
- Continuously monitor, assess, and manage project statuses to ensure timely and cost-effective achievement of project objectives.
- Proactively identify project resource needs, anticipate potential issues, and devise strategies for resolution to ensure successful project outcomes.
Qualifications:
- A focus on health-related fields is advantageous.
- A PhD degree is preferred.
- Completion of additional clinical research education (e.g., ACRP, SoCRA) is beneficial.
- Experience in medical translation is required.
- Comprehensive understanding of clinical trial and drug development processes, including ICH-GCP, FDA, and TPD regulatory requirements.
- Proven ability to manage multiple projects and cross-functional teams effectively.
We encourage applications from women and persons with disabilities.