• Independently manage and monitor assigned investigator sites from initiation to database lock. • Ensure compliance with Study Monitoring Plans, SOPs, GCP guidelines, and prevailing laws. • Partner with Site Care Partners prior to site activation on crucial feasibility and site selection processes, Pre-Trial Assessments (PTAs), site activation checklists, Informed Consent Document (ICD) finalization, and Site Initiation Visits (SIVs). • Actively mentor and train Clinical Research Associates (CRAs) as assigned, supporting their development and operational capability. • Serve as a Subject Matter Expert (SME) for CRA-related processes and participate in regional or local working groups and process improvement initiatives. • Identify, resolve, and manage complex investigator site issues. • Establish and implement robust CAPAs, manage Quality Event remediations, support sponsor regulatory interactions/inspections, and drive Audit Observation CAPA developments. • Partner with SCPs, Country SOMs, Clinicians, Recruitment Specialists, and Clinical Data Scientists. • Monitor site-level AEs/SAEs, collaborate with the Drug Safety Unit, handle investigational product oversight (accounting, storage, destruction), support database release, and conduct co-monitoring activities as requested.

• Coordinate and support clinical trial activities, assisting managers in their execution. • Contribute to project tasks and milestones, organizing work to meet deadlines. • Work in a structured environment using established procedures, seeking guidance from colleagues. • Maintain the Pfizer Trial Master File (PTMF) in compliance with ICH-GCP and SOPs, and ensure team members update tracking and files as needed. • Timely update trial and site information in the Corporate Clinical Trial Registry and support Clinical Trial Applications to ethics committees and regulatory authorities. • Provide administrative support for protocols and Informed Consent Documents (ICD) to global Project Managers and Study Managers, assisting with activities within set timelines. • Develop and maintain local tracking spreadsheets for study-related documents, data, and activities, prepare supportive materials for sites, attend training programs, and identify process improvements for inspection readiness and PTMF compliance.

• Conduct original research to determine thresholds of support or opposition for future and existing woodland caribou recovery efforts in complex, cross-cultural settings in Alberta and British Columbia. • Determine whether predator control is ever an acceptable management option in different scenarios involving woodland caribou in both provinces. • Assess public awareness of and support for woodland caribou associated predator removal programs. • Identify and characterize Indigenous and non-Indigenous perspectives and preferences for predator removal programs. We will elicit value orientations, attitudes, beliefs, and preferences to understand what influences these perspectives. • Explore the practical and theoretical basis for wildlife ethics- and equity-informed policies on woodland caribou conservation (e.g., having to stop a predator removal program based on evidence of public opposition even if that program is having successful impacts on the endangered species). • Co-ordinate the design of online surveys, including literature reviews, supporting University of Alberta Research Ethics Board submissions, testing and pilot phases, survey launch and quality assessment monitoring. • Carry out multivariate statistical analysis (e.g., factor analyses, econometric analyses) as appropriate to explore variables (social-psychological, preferences) associated with woodland caribou recovery and habitat conservation, and the ethics of predator control as a management approach. • Author and co-author peer-reviewed publications in high-impact journals to advance knowledge about conservation and wildlife management; and facilitate knowledge transfer through workshops, webinars, technical reports, and conferences to communicate research findings to diverse audiences. • Integrate the University of Alberta's Access, Community, and Belonging (ACB) framework into research activities, ensuring diverse perspectives are considered in stakeholder engagement and tool development.

• Monitors clinical trials and observational studies ensuring protocol adherence, managing site activities, and overseeing data collection and integrity. • Ensures sites are conducting the study(ies) and reporting study data as required by applicable regulations and guidelines, and sponsor requirements. • Performs remote and on-site monitoring in accordance with project specific timelines. • Completes travel scheduling in accordance with project specific and UBC travel policy. • Submits expense reports within UBC requirements. • Attends project team meetings, department meetings and one-to-one meetings with the manager. • Completes site monitoring reports and letters per UBC and/or sponsor SOPs requiring minimal corrections. • Ensures follow-up of site issues and action items per UBC/sponsor timelines. • Enters site visits, site monitoring reports, follow up letter sent date and site contacts into Clinical Trial Management System (CTMS). • Monitors within Electronic Data Capture (EDC) data entry, if applicable, and assists sites with electronic Case Report Form (eCRF) resolution. • Reviews Investigator Site File and performs Investigational Product reconciliation. • Maintains regular contact with assigned sites per study requirements. • Completes all SOP review, training assessments and documentation within requested timelines. • Travel up to 50% required in the European region. • Completes Site Management and Monitoring activities in accordance with project specific plans and timelines. • Assists with other duties as assigned, which may align with other departments at UBC.