30 Clinical Operations Management jobs in Toronto.

Burlington

• Skills: Clinical Trials, CRA, Functional Service Provider, Site Monitor, Country Study Operations Manager, Site Care Partner, Investigator Contracts Lead, Senior CRA, Project Leader, Biostatistical

Toronto

• Skills: clinical research, GI studies, patient identification, recruitment, enrollment techniques, retention plans, protocol, patient pathway, documentation, support
• Experience: experience in clinical research and GI studies

Burlington

• Skills: Clinical Trials, Functional Service Provider, Project Leadership, Biostatistics, Data Management, Clinical Research, Risk Management, Project Plans, Compliance, GCP

Toronto

• Skills: clinical research, quality compliance, ICH GCP, audits, CAPA, quality metrics, training compliance, investigational methods, risk management, regulatory requirements
• Experience: 7+ years of related experience
• Type: Full-time

Toronto

• Skills: clinical research, cardiovascular disease, questionnaires, surveys, recruitment, data reporting, climate change, patient interaction, study coordination, REDCap
• Type: Temporary Part-time

Toronto

• Skills: regulatory, clinical trials, ethics applications, sponsor liaison, start-up process, document management, timelines, compliance, SOPs, regulatory requirements

Toronto

• Skills: clinical trials, contract negotiation, budgeting, investigators, external vendors, contracts, protocols, compliance, negotiation, clinical site
• Experience: At least 2 years in site contract negotiation
• Type: Full-time

Toronto

• Skills: clinical trial procedures, regulatory management, team management, quality assurance, study coordination, budget development, study expenses, training, standard operating procedures, resource management
• Type: Full-time

Toronto

• Skills: Project Management, clinical trials, Radiopharmaceuticals, Gastrointestinal, Lung, Breast Cancer, Duchenne Muscular Dystrophy, ALS, Stargardt’s, regulatory standards
• Type: Contract

Toronto

• Skills: clinical trials, regulatory compliance, data collection, patient enrollment, research management, monitoring visits, ICH-GCP, study protocols, healthcare, clinical research
• Type: full_time

Brampton

• Skills: Research Coordinator, Oncology, Clinical Trials, Patient Screening, Data Collection, Ethical Conduct, Clinical Research, Microsoft Office, Health Regulations, Patient Care
• Type: full_time

Toronto

• Skills: Research Ethics, Clinical Trials, Biomedical Research, Protocol Management, Ethical Standards, Investigators Liaison, Regulatory Compliance, Good Clinical Practice, Documentation, Organizational Skills
• Type: temporary

Toronto

• Skills: clinical trial management, project management, Good Clinical Practice, regulatory requirements, study milestones, investigator selection, subject recruitment, data systems, team leadership, risk assessment
• Type: full_time

Toronto

• Skills: clinical trials, research management, Ophthalmology, study coordination, protocol submissions, regulatory compliance, quality assurance, data management, team leadership, healthcare research
• Type: temporary

Toronto

• Skills: Clinical Research, Cardio-oncology, Data Management, Study Coordination, Patient Recruitment, ICH/GCP Guidelines, Adverse Events, Regulatory Compliance, Research Ethics, Budgeting
• Type: full_time

Mississauga

• Skills: clinical research, study startup, site activation, project tracking, IRB submission, budgets, documentation, audit preparation, feasibility research, project communication
• Type: full_time

Mississauga

• Skills: contract management, clinical trials, negotiation, budgets, ethical practices, regulatory compliance, clinical study sites, stakeholder communication, audit support, process improvements
• Type: full_time

Toronto

• Skills: Pharmacovigilance, Project Management, Medical Information, Quality Assurance, Regulatory Affairs, Communication, Leadership, Problem Solving, Training, Development
• Type: other

Toronto

• Skills: Clinical Research, Phase I Clinical Trials, Informed Consent, Adverse Events, Data Collection, Patient Management, Clinical Trials Coordination, Oncology, Documentation Practices, ICH/GCP Guidelines
• Type: full_time

Toronto

• Skills: Project Manager, Clinical trials, CRO, Radiopharmaceuticals, ALS, Regulatory standards, Project plans, Study organization, Stakeholder management, Training programs
• Type: contract