Top Research Jobs in Vancouver

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.

The Director of Research for Power Markets will oversee the QA/QC process for long-term price forecasts and act as an advisor to leadership, ensuring rigorous review and internal expertise engagement throughout the forecasting cycle.

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.

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.

Perform routine entry-level histology and lab support tasks including preparing specimens from paraffin blocks, labeling and tracking slides, inventory and equipment maintenance, reagent preparation, basic data entry, receiving/logging specimens, and assisting senior technical staff with routine laboratory duties.

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.

Coordinate recruitment, consent, scheduling, data collection and storage for a clinical sexual-health study. Operate and troubleshoot VR testing equipment, train/oversee volunteers, prepare ethics amendments, manage study documentation and finances, and provide administrative support to the PI including manuscript and presentation assistance.

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.

Provide administrative and study support for the Clinical Trials Unit and pediatric oncology investigators: scheduling, records and database maintenance, onboarding, recruitment support, study coordination (enrollment, data capture, specimen management), regulatory compliance, audit support, reporting, and financial/resource tracking. Ensure protocol adherence, maintain study documents, and liaise with interdisciplinary teams, sponsors, and consortiums.

Perform computational biology and translational bioinformatics analyses to integrate multi-omics and imaging data, identify disease mechanisms and biomarkers, develop reproducible workflows and visualization tools, support experimental integration, prepare manuscripts/grants, and mentor trainees in a multidisciplinary ophthalmology research lab.

Support computational genomics research by processing and quality-controlling high-throughput sequencing data, performing SNV calling and microbiome profiling, benchmarking variant callers, developing reproducible Bash/Snakemake workflows, documenting analyses, supervising undergraduates, conducting literature reviews, and preparing statistical reports for the lab.

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.

Conducts cancer pathology research using histology, immunohistochemistry, in situ hybridization, digital pathology, microscopy, tissue microarrays, and FFPE specimens. Responsibilities include tissue processing, staining, slide scanning, macrodissection, equipment maintenance, sample tracking, inventory management, researcher training, safety compliance, and coordination with vendors. The role supports multidisciplinary research projects under principal investigator and facility lead supervision.

Manages multiple market research projects from client objectives through fieldwork, validation, analysis, and reporting. Conducts statistical analysis, monitors data integrity and quality standards, develops reporting plans, and translates findings into clear, actionable insights. Collaborates with internal teams and clients, presents results, manages deadlines, and resolves project issues while applying data, digital, and AI tools.

Graduate research interns will own end-to-end projects developing customer world models and proactive intelligence. Work spans representation learning, foundation models, reinforcement learning, agentic decision systems, and evaluation. Tasks include designing methods, running experiments, publishing findings, and potentially shipping models into production to impact customer-facing products.

Lead development and flight-test of long-range medical drone autopilots and planners. Design control algorithms and embedded flight software (C/C++, ROS/ROS2), integrate onboard edge computing and GPS/teleoperation, perform HIL and field testing, analyze flight safety/performance data, prepare regulatory filings and technical reports, and coordinate with industry, community, and health-system partners.

Lead end-to-end consumer research projects: design methodology and questionnaires, analyze complex datasets, validate data, synthesize insights, write and present client reports, manage timelines and stakeholder communications.

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.

Work on designing, implementing, and improving state-of-the-art reinforcement and imitation learning algorithms for dexterous robotic manipulation. Develop RL/IL training and data-collection pipelines, integrate ML models onto robotics platforms, evaluate sim-to-real transfer, and collaborate across teams to deploy algorithms on physical humanoid robots.

Lead development of cutting-edge RL and imitation-learning algorithms for dexterous robotic manipulation, design training and large-batch simulation pipelines, enable sim-to-real transfer, integrate models onto physical robots, and drive research from experimentation to production while mentoring and collaborating across teams.