Regional Clinical Research Site Manager

This position function will oversee operations and quality at GTA sites (Hamilton, Mississauga,Toronto, Scarborough), as well as provide backup CRC support (with focus on Toronto and Scarborough). Additionally, this position will operationally support growth projects, ie. opening of new locations, implementation of tech systems, initiationof new therapeuticarea. CRP supervision and training: Support with interviewing and hiring of CRPs across GTA locations Personnel management of CRCs(3-4)and RAs(1)across GTA locations, including regular 1:1 and group meetings Coordinate and conduct training sessions to support growth and development of CRPs Quality management & process refinement: Review IMV follow up letters and coordinate action based on trends detected Oversee the CAPA process for all identified MPDs Conduct internal audits as needed Prepare for and lead the conduct and response to external audits and inspections Own company-wide adherence to SOPs and GCP guidelines; continually refine and develop the set of SOPs,formsand source templates Support with source document creation and quality check, where needed Operations oversight: Oversee CTMS visit tracking and scheduling across all sites Regularly run CTMS reports to oversee operations trends and support in evaluation of CRP performance Have a pulse oneISFand coordinateclean-upefforts where necessary Identifyareas of operational or quality risk and coordinate with leadership on plan of action Support in study builds within CTMS, where needed Backup CRC and lab support: Support where operationally necessary as a backup CRC/lab tech, with focus on Toronto and Scarborough locations Investigator relationship management: Regularlytouch basewith PI’s and SI’s across all sites, incorporating their feedback into our workflows and ensuring frictionless research referrals Support in the engagement of potential new research investigators, including onboarding them to research through basic training elements

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