Clinical Research

• Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites
• Generate visit and contact reports
• Build and maintain site relationships as the primary site contact
• Address and resolve site issues and questions
• Oversee study integrity and site delivery from identification through close-out
• Review trial performance and safeguard human-subject rights and well-being in accordance with the protocol
• Develop patient recruitment strategies with clinical sites to meet enrollment timelines
• Ensure compliance with SOPs, protocols and amendments, GCP, and applicable regulatory requirements
• Evaluate reported-data quality and integrity, site efficacy, and drug accountability
• Monitor completeness and quality of regulatory documentation
• Perform site document verification

Clinical Research Associate – Senior, Bilingual French/English

• Lead the operational delivery of assigned clinical trials, ensuring milestones, timelines, budget expectations, and quality standards are achieved
• Drive study start-up activities, site activation, enrollment strategies, and study execution through database lock
• Provide oversight of study progress, monitoring activities, clinical metrics, and site performance
• Develop and implement effective study oversight plans, monitoring strategies, and risk mitigation approaches
• Identify operational challenges and proactively implement solutions to ensure successful study delivery
• Build and maintain strong relationships with sponsors, investigators, vendors, and cross-functional stakeholders
• Review study performance metrics and provide regular status updates and reporting
• Support, mentor, and collaborate with Clinical Research Associates (CRAs) and other study team members
• Ensure all clinical trial activities comply with protocol requirements, ICH-GCP guidelines, and applicable regulatory requirements

Senior Clinical Trial Manager

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolution of queries to maintain high-quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
• Design and analyse clinical trials, interpret complex medical data, and contribute to innovative treatments and therapies.
• Take responsibility for deliverables and work collaboratively in a sponsor-dedicated model.

Clinical Research Associate

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborate with investigators and site staff to facilitate smooth study conduct
• Perform data review and resolution of queries to maintain high-quality clinical data
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports
• Design and analyse clinical trials, interpret complex medical data, and contribute to innovative treatments and therapies
• Take responsibility for clinical trial monitoring deliverables and work collaboratively in a sponsor-dedicated model

• Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
• Lead clinical trial monitoring tasks with a focus on quality and continuous improvement
• Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice standards
• Conduct site visits to assess site performance, resolve issues, and provide support
• Collaborate with cross-functional teams on timely and accurate data collection and reporting
• Provide training and guidance to site staff and other CRAs
• Build and maintain relationships with site personnel and stakeholders
• Monitor respiratory and cardiovascular studies in the GTA area

• Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
• Lead clinical trial monitoring tasks with a focus on quality and continuous improvement
• Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and GCP standards
• Conduct site visits to assess site performance, resolve issues, and support successful trial execution
• Collaborate with cross-functional teams on timely and accurate data collection and reporting
• Provide training and guidance to site staff and other CRAs
• Build and maintain relationships with site personnel and stakeholders
• Monitor respiratory and cardiovascular studies in the Greater Toronto Area

• Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
• Lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
• Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
• Conduct site visits to assess site performance, resolve issues, and support successful trial execution
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
• Provide training and guidance to site staff and other CRAs
• Build and maintain relationships with site personnel and stakeholders to facilitate smooth trial operations
• Monitor respiratory and cardiovascular studies in the Greater Toronto Area

Senior Clinical Research Associate

• Author and contribute to clinical and regulatory documents, including study protocols, statistical analysis plans, clinical study reports, narratives, abstracts, posters, and manuscripts
• Contribute to study design and review informed consent forms
• Review statistical analysis plans and tables, figures, and listings
• Review, analyze, and interpret study data
• Perform online literature searches
• Prepare and review training materials for scientific teams and the company
• Manage medical writing deliverables, stakeholder communication, project issues, and timelines
• Provide scientific, therapeutic, and medical writing expertise during study conduct
• Mentor and train new and junior staff
• Perform quality-control reviews of documents prepared by team members
• Support delivery of scientific affairs commitments on time, within budget, and in compliance with SOPs and regulations
• Contribute to organizational improvements and implementation of new processes and procedures
• Participate in QA or client audits as a scientific subject-matter expert
• Support business development with proposal synopses, bid-defense content, sponsor meetings, and sponsor questions
• Review scientific-affairs assumptions and budgets during RFPs
• Provide scientific support and medical writing for pre-IND and IND submissions
• Provide scientific expertise and potentially lead cross-functional projects
• Perform other assigned responsibilities when qualified and trained

Senior Clinical Scientist

• Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
• Lead clinical trial monitoring tasks with a focus on quality and continuous improvement
• Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
• Conduct site visits to assess performance, resolve issues, and support successful trial execution
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
• Provide training and guidance to site staff and other CRAs
• Build and maintain relationships with site personnel and stakeholders
• Monitor cardiovascular and respiratory studies in Quebec

• Manage day-to-day clinical trial management activities, supporting the team to deliver quality outcomes
• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures
• Build and manage relationships with trial investigators and stakeholders
• Ensure trials comply with local, national, and international regulations and ethical guidelines
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management
• Support the development of the team and manage competing priorities

Clinical Research jobs in Canada

Clinical Research Associate – Senior, Bilingual French/English

Senior Clinical Trial Manager

Clinical Research Associate

Clinical Research Associate

Clinical Research Associate

Clinical Research Associate

Senior Clinical Research Associate

Senior Clinical Scientist

Clinical Research Associate

Lead Clinical Research Associate