Job Title

Company Description We are the company that cares for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800+ driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description Hybrid role in Mississauga, ON, Canada. Site Management. Responsibilities Ensures exchange of information and documentation with sites and vendors Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies Ensures regulatory and ethics committee submissions and notifications Ensures proper administration of sites and vendors payments Coordinates preparation for and follow-up on site, TMF and systems audits and inspections Reviews and coordinates site-specific query resolution Reviews and coordinates site-specific EDC completion and provides the site Monitor with regular updates on the completion status Other Communications Exchanges information and documentation with other departments Supports the organization of internal team meetings including preparation of agendas and minutes Supports the organization of Investigator Meetings Maintains study-specific and corporate tracking systems Serves as the sites primary contact point Serves as the primary sites contact point for vendors, study supplies, and access management Ensures communication between the sites and off-site facilities Training Arranges and tracks initial and on-going project training for site teams in all vendor-related systems Provides training in courier management and study supplies ordering to the site team Document Management Checks the TMF on a site and a country level regularly and files pending documents Prepares, distributes, and updates Investigator Site Files (ISF) and ISF checklists Provides Monitors with ISF documents to be filed in the ISF prior to each monitoring visit Revises and checks translations status Safety Management Ensures proper safety information flow with the investigative sites. CTMS Management Updates CTMS with lacking project information Assists the Monitors in their prompt completion of all subject event and site event information in CTMS Assists the Monitors in their meeting deadlines for site visits, visit reports and visit letter dates information recording in CTMS Tracks the resolution status of site issues and action items in CTMS Vendor Management Ensures that pre-study testing (dummy scans, MRI/CT qualification questionnaires, test ECGs, etc.) of local site facilities is completed Tracks vendor-related supplies (lab kits, ECG electrodes, CDs for scans, etc.) on a site level Additional Information All your information will be kept confidential according to EEO guidelines. Seniority level: Associate Employment type: Full-time Job function: Administrative Industries: Pharmaceutical Manufacturing #J-18808-Ljbffr