Top Research Jobs in Vancouver

Manages, monitors, and closes assigned clinical trial sites, ensuring patient safety, protocol compliance, data quality, regulatory adherence, and timely study delivery. Responsibilities include site relationship management, recruitment support, onsite and remote monitoring, adverse event follow-up, investigational product oversight, issue resolution, audit and CAPA support, reporting, and database release. The role also mentors clinical research associates, supports site activation and feasibility activities, and participates in process improvement initiatives.

Manages, monitors, and closes assigned clinical trial sites from initiation through database lock. Ensures patient safety, protocol compliance, data quality, regulatory adherence, recruitment progress, investigational product accountability, and timely issue resolution. Serves as the primary site contact, conducts onsite and remote monitoring, supports audits and CAPA activities, trains site personnel, resolves data queries, and collaborates with investigators, vendors, drug safety teams, and study stakeholders. The role also mentors Clinical Research Associates and contributes to process improvement initiatives.

Graduate research interns will own end-to-end projects to build customer world models and proactive intelligence: developing representation learning, foundation model, RL/agentic methods, evaluation frameworks, and shipping research into production to improve customer decision-making.

The Director of Innovation Management leads a team to drive innovative solutions for mountain athletes, managing a long-term innovation portfolio and overseeing product commercialization from concept to market.

Lead Benevity’s product research practice, setting strategy, standards, and operating processes while shaping the research team. Conduct qualitative and quantitative studies, including employee and nonprofit tracking, and integrate AI into research synthesis and repository workflows. Partner with analytics, product, design, and leadership teams to influence roadmaps and executive decisions. Establish ethical research and AI guardrails, coach non-researchers, facilitate discovery sessions, and communicate actionable behavioral and feedback insights.

Lead and evolve Benevity’s product research practice, connecting qualitative and quantitative insights to product roadmap decisions. Oversee research strategy, intake, methodologies, tracking studies, repositories, and executive reporting. Integrate AI into research workflows with appropriate guardrails, build AI-enabled research skills, and partner with analytics teams. Coach product managers and designers, facilitate Discovery Lab sessions, represent diverse user perspectives, and grow the research function over time.

Provides high-level administrative support for Arts research centres, including student appointments, payroll and HR inquiries, onboarding, events, meetings, communications, website updates, proposal tracking, records administration, and special projects. The role requires policy knowledge, discretion, accuracy, coordination, document preparation, inquiry response, and support for faculty, staff, and students. It may also provide training and task supervision to Work Learn students.

Lead strategic and operational management of a multi‑project neuroimmunology research portfolio for the UBC Chair in Multiple Sclerosis. Responsibilities include program planning, ethics and grant submissions, budget and resource management, stakeholder and partner engagement, regulatory compliance, staff oversight, communications, and knowledge mobilization to advance basic, translational, and clinical research.

Support an observational epidemiological stroke study by reviewing charts, entering and maintaining confidential study data, preparing ethics submissions, coordinating imaging requests and deidentification, and liaising with clinicians, patients, and the research team to ensure study operations and regulatory compliance.

Develops and optimizes upstream and downstream bioprocesses for plasmids, mRNA-LNP, cell therapies, biologics, and related therapeutics. Designs experiments, analyzes process data, performs scale-up calculations, develops protocols and GMP-aligned documentation, evaluates equipment and technologies, and supports technology transfer to GMP production. The role also coordinates with scientists, quality teams, vendors, and manufacturing staff, while mentoring junior personnel and contributing to reports, publications, and presentations.

Supports qualitative health professions education research by revising study materials, recruiting participants, conducting interviews and body mapping, coordinating data collection, transcribing and analyzing data, performing literature reviews, and helping prepare reports, presentations, and manuscripts. Maintains confidential research data in accordance with ethics protocols and institutional policies while providing administrative and logistical support to investigators.

Supports tuberculosis research studies at a provincial TB clinic by recruiting and screening participants, obtaining consent, scheduling visits, collecting data, arranging samples, administering honoraria, maintaining study documentation, and ensuring protocol and regulatory compliance. Communicates with healthcare professionals, reports procedural issues, participates in training and meetings, and assists with research progress reports under direct supervision.

Conducts advanced statistical analysis, predictive modeling, institutional research, forecasting, survey design, and data reporting to support university planning and executive decision-making. Responsibilities include extracting and validating sensitive data, developing dashboards and performance metrics, leading complex research projects, presenting findings, liaising with government and academic stakeholders, troubleshooting reporting systems, mentoring analysts, and ensuring analytical quality and integrity.

Provide research and program support for CPD educational initiatives, including study and evaluation design, literature reviews, data collection and analysis, survey development, report writing, Moodle course support, event coordination, and translating findings into program improvements.

Conducts clinical research activities involving people living with Parkinson’s, including participant recruitment, eligibility screening, cognitive and motor assessments, data collection and entry, biological sample tracking, and study visits. Maintains ethics and regulatory documentation, supports UBC CREB and VCHRI approvals, troubleshoots study issues, and assists with administrative tasks across laboratory studies.

Assists Cardiology quality improvement and research projects by conducting chart reviews, collecting and extracting patient data, entering information into Excel and REDCap, performing descriptive analyses, maintaining databases and reports, coordinating meetings, preparing minutes, formatting materials, and contributing to presentations and publications. Requires discretion when handling confidential patient data and the ability to work independently under general supervision.

Coordinates a provincial cardiovascular research study across two hospital sites. Responsibilities include participant recruitment, informed consent, scheduling, follow-up, study operations, regulatory and Research Ethics Board submissions, protocol compliance, data management in REDCap, specimen collection and shipment, literature reviews, documentation, and communication with investigators, clinical teams, participants, sponsors, and regulators. The coordinator also supports SOP development, research proposals, publications, and conference presentations while ensuring ethical conduct, confidentiality, and Good Clinical Practice compliance.

Supports biobanking and movement-disorders research by collecting, processing, preserving, logging, shipping, and cataloging human biospecimens. Performs experiments, cell and tissue procedures, data collection, database management, participant consent and questionnaires, equipment maintenance, inventory ordering, SOP development, and biosafety and ethics compliance. The role works independently onsite and interacts frequently with study participants and collaborating laboratories.

The Mid-Level Research Program Manager will lead and manage research and technology transfer activities, build collaborative relationships, prioritize projects for funding and ensure successful program implementation.

Serve as primary contact between investigational sites and sponsor; perform site selection, initiation, routine monitoring, and close-out; ensure ICH‑GCP and Health Canada compliance; maintain CTMS/eTMF documentation; monitor safety reporting (AE/SAE/PQC); support recruitment, drug accountability, data query resolution, site budgets/payments, and escalate risks to the clinical team.

Coordinates a provincial cardiovascular research study involving echocardiography, genomics, and AI. Responsibilities include participant recruitment, informed consent, scheduling, follow-up, multi-site study operations, regulatory and ethics submissions, protocol compliance, data and specimen management, literature reviews, and research documentation. The coordinator works with investigators, clinical teams, hospital staff, participants, sponsors, and regulators, while supporting data integrity, adverse-event reporting, SOP development, and potential publications and presentations.

Coordinates a provincial cardiovascular research study across Richmond and Delta Hospitals. Responsibilities include participant recruitment, informed consent, scheduling, follow-up, study-site operations, regulatory and ethics submissions, protocol compliance, data management, specimen coordination, literature reviews, SOP development, and research reporting. The coordinator works with investigators, clinical teams, participants, sponsors, and regulatory bodies while maintaining accurate documentation, confidentiality, and Good Clinical Practice standards.

Coordinates a provincial cardiovascular research study across two hospital sites. Responsibilities include participant recruitment, informed consent, scheduling, follow-up, study operations, regulatory and ethics submissions, protocol compliance, data management in REDCap, biological specimen coordination, literature reviews, SOP development, and research reporting. The coordinator collaborates with investigators, clinical teams, participants, sponsors, and regulators while maintaining accurate documentation, confidentiality, and Good Clinical Practice compliance.

Lead advanced AI research projects focused on computer graphics and rendering techniques, mentoring junior engineers and translating ideas into research prototypes.

Lead quantitative research projects end-to-end, design proposals, analyze large datasets, prepare reports and presentations, advise clients strategically, mentor junior staff, support business development, and manage account-level client relationships.