Role Description 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. - Thorough knowledge and application of project specific protocol - 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 The following duties are required for monitoring in the European region: - Performs review and updates Patient Information Sheet and Informed Consent as per local legislation and requirements. - Translation from/into local language into/from English for complete study specific communication as needed. - Preparation, submission and tracking of CTIS, Competent Authority, Central and Local Ethics Committee and other regulatory applications as required. - Conducts Contract negotiations with Sites, Foundations, and local Research & Development Departments in collaboration with the Contract Management team. - Reviews and confirms details of payments for sites to be paid as per contract in collaboration with the team - Maintenance of eTMF and tracks collection of essential documents - Conducts Study feasibility assessments with sites Qualifications - Bachelor’s degree – Life Science preferred or equivalent years of industry and clinical research experience - Minimum of 24 months’ clinical research experience, specifically in site management and remote monitoring - Preferably at least 6 months’ on-site monitoring experience - Knowledge of medical terminology and regulatory guidelines, including local legislation - Strong attention to detail, excellent organizational skills, and the ability to communicate effectively are essential - Excellent critical thinking and resolution skills - Proven ability to deliver accurate work and adhere to deadlines in a fast-paced environment - Good written and verbal communication skills in English and local language (as applicable) - Experience and familiarity with CTMS, eTMF, EDC, Microsoft Office applications Company Description UBC is proud to be an equal opportunity employer and does not discriminate because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state, or local protected class. We are committed to a diverse, equitable and inclusive culture that fosters respect for each other, our clients, and our patients.

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description As a senior research analyst at Harris, you will have the opportunity to create high-impact, externally facing thought leadership that solves client challenges and shapes industry conversations. Primary day-to-day responsibilities will revolve around: - Helping concept and create story-driven research programs - Managing the dynamic project fulfillment process - Owning the analysis and narrative development of findings Key components of this position include: - Creative concepting and ongoing trend monitoring - Cultural exploration and ensuring job quality - Overseeing the execution of the research process across our operations team Many projects are designed for external audiences, including media, PR, and executive thought leadership platforms—requiring strong storytelling instincts, strategic framing, and a focus on producing compelling, headline-ready insights. Given the entrepreneurial nature of the company, you will have the opportunity to gain experience in areas beyond "day-to-day" consulting projects such as: - Business development and strategy - Thought leadership - Media- and PR-oriented research - Product/service innovation Working with the thought leadership team, you will also have the unique opportunity to propose creative solutions to client problems and take ownership of new research ideas from concept through execution and storytelling. Specific Responsibilities: - Manage end-to-end project schedules, timelines, and key milestones - Contribute to research concepting, strategic framing, and story angles - Write surveys and research instruments from outlines with moderate oversight, ensuring clarity, flow, and strong insight potential - Manage the project and project quality through fielding - Prepare field progress updates and performance summaries for internal teams and clients - Prepare and populate report templates, ensuring accuracy, consistency, and high-quality outputs - Write detailed findings and translate data into clear insights, implications, and strategic narratives - Participate in client discussions, readouts, and presentations - Proactively support client research needs and goals, bringing fresh ideas, emerging trends, and innovative approaches to each engagement - Work across multiple client accounts simultaneously and manage time accordingly Qualifications - A bachelor’s degree: concentrations or interest in journalism, sociology, business or marketing are also a plus - 2+ years of experience in market research, marketing, management consulting, media planning, media buying, strategic planning, investment banking, data journalism or other related functions - Excellent quantitative and analytical skills - Outstanding written and verbal communication skills, including the ability to independently author reports, storylines, and presentations - A natural curiosity about consumer behavior, cultural shifts, and emerging trends - Interest in monitoring news, social trends, and industry developments to inform research and spark new thought leadership ideas - An appetite to work across a variety of categories, topics and project types - Ability to interface effectively with multiple levels of management, ranging from senior corporate executives to business unit managers and third parties - Ability to work as part of a team and support and guide junior analysts when needed - Strong attention to detail paired with big-picture strategic thinking - Comfort working in a fast-paced, entrepreneurial environment where ownership and initiative are valued - Experience translating data into media-friendly insights, headlines, or story angles is a plus - Familiarity with thought leadership research or PR-driven studies also a plus Requirements - In order to comply with equal pay and salary transparency laws in various locations, we believe the target range of base compensation for this role is $70,000 - $75,000. - Actual compensation is influenced by a wide array of factors including but not limited to skill set, level of experience, and location.

• Independently manage assigned clinical trial sites from start-up through close-out • Perform site qualification, initiation, routine monitoring, and close-out visits • Ensure subject safety, data integrity, and protocol compliance at all assigned sites • Review source documentation, CRFs, and EDC entries for accuracy, completeness, and timeliness • Serve as the primary point of contact for investigators and site staff • Build strong, collaborative relationships with site teams • Identify site performance issues early and implement corrective actions • Ensure compliance with ICH GCP, FDA regulations, ISO 14155 (as applicable), and internal procedures • Support audits and inspections as a subject matter expert • Mentor and provide functional guidance to junior CRAs and CTAs • Partner closely with Clinical Operations, Quality, Regulatory, Data Management, and Medical Affairs

• Supporting the Test Resource Management Center’s (TRMC) Big Data (BD) and Knowledge Management (KM) Team • Analyzing DoD Test & Evaluation data • Developing data-driven decision analysis products • Collaborating with technical and non-technical stakeholders • Communicating data-based insights in written or presented form • Providing technical support for CHEETAS and other tools • Running hands-on training sessions with end users • Operating remotely with potential travel requirements