Statistician
Montreal, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life ...
Statistician
Montreal, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life ...
... Management, Test and Trials (T&Ts), Security, Safety, Electromagnetic Interference (EMI)/Electromagnetic Compatibility (EMC) or Environmental Qualification.
... Management, Test and Trials (T&Ts), Security, Safety, Electromagnetic Interference (EMI)/Electromagnetic Compatibility (EMC) or Environmental Qualification.
Statistician
Sherbrooke, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life ...
Statistician
Sherbrooke, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life ...
Experience with Change Management, Requirements Management, Test and trials, Security, Safety Familiarity with of Dynamic Object-Oriented Requirements System (DOORS) (IBM Rational) Familiarity with ...
Experience with Change Management, Requirements Management, Test and trials, Security, Safety Familiarity with of Dynamic Object-Oriented Requirements System (DOORS) (IBM Rational) Familiarity with ...
Systems Engineer Associate
Montreal, QC · On-site
... Management, Test and Trials (T&T), Security, Safety, Electromagnetic Interference (EMI)/Electromagnetic Compatibility (EMC) or Environmental Qualification.
Systems Engineer Associate
Montreal, QC · On-site
... Management, Test and Trials (T&T), Security, Safety, Electromagnetic Interference (EMI)/Electromagnetic Compatibility (EMC) or Environmental Qualification.
CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada
Montreal, QC · Remote
... clinical trials and respond to emergency situations based upon clinical research standards ... Responsible for all aspects of site management as prescribed in the project plans * General On-Site ...
CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada
Montreal, QC · Remote
... clinical trials and respond to emergency situations based upon clinical research standards ... Responsible for all aspects of site management as prescribed in the project plans * General On-Site ...
Cardiologist (strongly preferred)with cardiovascular outcome trials or large complex, global ... Management experience - Able to work ina highly complexmatrixed environment and able to influence ...
Cardiologist (strongly preferred)with cardiovascular outcome trials or large complex, global ... Management experience - Able to work ina highly complexmatrixed environment and able to influence ...
Manage claims in litigation, participate in mediations, pre-trials and settlement conferences * Perform other tasks and duties as assigned by the Unit Manager Please note, salary range is not ...
Manage claims in litigation, participate in mediations, pre-trials and settlement conferences * Perform other tasks and duties as assigned by the Unit Manager Please note, salary range is not ...
Manage claims in litigation, participate in mediations, pre-trials and settlement conferences * Perform other tasks and duties as assigned by the Unit Manager Salary range is not inclusive of total ...
Manage claims in litigation, participate in mediations, pre-trials and settlement conferences * Perform other tasks and duties as assigned by the Unit Manager Salary range is not inclusive of total ...
34834
Quebec, QC · On-site
CA$71K - CA$82K/yr
Own the end-to-end testing process, including the management of proof-of-concepts (PoC) and rigorous "real-world" trials. * Sales Enablement: Act as a technical advisor to the Sales team, providing ...
34834
Quebec, QC · On-site
CA$71K - CA$82K/yr
Own the end-to-end testing process, including the management of proof-of-concepts (PoC) and rigorous "real-world" trials. * Sales Enablement: Act as a technical advisor to the Sales team, providing ...
Product Specialist - HV Power
Saint-michel, QC · On-site +1
Work closely with Product Management, Engineering, Operations and Technical Support teams to ... Support product trials, testing programmes and first-of-type installations across Europe. * Share ...
Product Specialist - HV Power
Saint-michel, QC · On-site +1
Work closely with Product Management, Engineering, Operations and Technical Support teams to ... Support product trials, testing programmes and first-of-type installations across Europe. * Share ...
... use during clinical trials. * Assign equipment asset tags to newly inventoried equipment ... Proactively communicate issues and problem resolutions to departmental supervisors and managers.
... use during clinical trials. * Assign equipment asset tags to newly inventoried equipment ... Proactively communicate issues and problem resolutions to departmental supervisors and managers.
Working with legal partners to manage litigation cases until their resolution; * Representing the company during discovery, mediation, arbitration, and trials; * Representing the company in Small ...
Working with legal partners to manage litigation cases until their resolution; * Representing the company during discovery, mediation, arbitration, and trials; * Representing the company in Small ...
Working with legal partners to manage litigation cases until their resolution; * Representing the company during discovery, mediation, arbitration, and trials; * Representing the company in Small ...
Working with legal partners to manage litigation cases until their resolution; * Representing the company during discovery, mediation, arbitration, and trials; * Representing the company in Small ...
Influencing - Able to manage and motivate internal teams on clinical trials. * Conflict Management - Able to act as mentor / coach to others to improve conflict management skills; steps up to ...
Influencing - Able to manage and motivate internal teams on clinical trials. * Conflict Management - Able to act as mentor / coach to others to improve conflict management skills; steps up to ...
Manage calendars and schedule appointments using Outlook and various planning tools. * Oversee and ... Schedule court appointments, trials, and judicial review hearings by coordinating with court ...
Manage calendars and schedule appointments using Outlook and various planning tools. * Oversee and ... Schedule court appointments, trials, and judicial review hearings by coordinating with court ...
Law Clerk
Montreal, QC · On-site
... trials. * Liaise with external counsel on Superior Court matters in Québec. * Work with the Toronto litigation team to manage Small Claims actions nationwide from start to finish, with ownership of ...
Law Clerk
Montreal, QC · On-site
... trials. * Liaise with external counsel on Superior Court matters in Québec. * Work with the Toronto litigation team to manage Small Claims actions nationwide from start to finish, with ownership of ...
Law Clerk
Montreal, QC · On-site
... trials. * Liaise with external counsel on Superior Court matters in Quebec. * Work with the Toronto litigation team to manage Small Claims actions nationwide from start to finish, with ownership of ...
Law Clerk
Montreal, QC · On-site
... trials. * Liaise with external counsel on Superior Court matters in Quebec. * Work with the Toronto litigation team to manage Small Claims actions nationwide from start to finish, with ownership of ...
To provide training to our account management team and customers on use of product * Help diagnose and guide internal and external customers through technical issues * Field test and trials of ...
To provide training to our account management team and customers on use of product * Help diagnose and guide internal and external customers through technical issues * Field test and trials of ...
Assisting lawyers in the preparation and coordination of hearings and trials; recording and ... Managing files including: opening new files, maintaining large and complex files, developing ...
Assisting lawyers in the preparation and coordination of hearings and trials; recording and ... Managing files including: opening new files, maintaining large and complex files, developing ...
Trials Manager information
What is a trials manager?
Trials Managers are professionals responsible for overseeing and coordinating clinical trials or research studies. They manage all aspects of the trial process, including planning, organizing, and ensuring that studies are conducted in accordance with regulatory guidelines and protocols. Their role often involves liaising with sponsors, investigators, and regulatory authorities, as well as monitoring progress and reporting results. Trials Managers play a key role in ensuring that trials are completed on time, within budget, and to the required quality standards.
What are the main challenges a trials manager faces when coordinating multi-site clinical trials?
As a Trials Manager, one of the primary challenges when overseeing multi-site clinical trials is ensuring consistent protocol adherence and data quality across all locations. This involves frequent communication with site staff, troubleshooting logistical issues, and monitoring regulatory compliance. Additionally, balancing timelines and resources while managing diverse teams can be demanding. Successful Trials Managers proactively address these challenges through robust planning, regular site visits, and clear documentation to keep studies on track.
What are the key skills and qualifications needed to thrive as a trials manager, and why are they important?
To thrive as a Trials Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a relevant scientific degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and often certifications like ACRP or SOCRA are highly valuable. Strong leadership, organization, and communication skills help manage multidisciplinary teams and ensure protocol adherence. These competencies are crucial for delivering safe, efficient, and compliant clinical trials that advance medical research.
What is the difference between Trials Manager vs Clinical Research Coordinator?
| Criteria | Trials Manager | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, experience in trial management, knowledge of regulations | Bachelor's degree, clinical research experience, regulatory knowledge |
| Work Environment | Oversees multiple trials, manages teams, coordinates with sponsors | Handles daily trial activities, patient interactions, data collection |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research institutions |
The Trials Manager focuses on overseeing entire clinical trials, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, working directly with patients and collecting data. Both roles require similar educational backgrounds and regulatory knowledge but differ in scope and responsibilities.
What are popular job titles related to Trials Manager jobs in Quebec?
For Trials Manager jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Trials Manager jobs in Quebec look for?
The top searched job categories for Trials Manager jobs in Quebec are:
Statistician
Montreal, QC • Remote
Alimentiv
Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 12 days ago
Job description
Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life cycle in accordance with project, organizational and regulatory standards. Act as subject matter expert, providing statistical support to project teams, quality/study auditors, and external stakeholders. Participate in the promotion of Alimentiv as a global research organization, by contributing to the development, publishing, and reporting of project data. Please note we are hiring for multiple positions at this time.
Analysis Services
- Carry out statistical analyses and provide direction to programmers, using standard software packages to interpret and translate results within a statistical framework into biomedical terms and prepare statistical data results for inclusion in reports and research papers that meet trial, organizational and regulatory best practices, and standards.
Academic Research Support
- Working in conjunction with the Director of Academic Research, convert and present new and novel biometrical trial technologies, processes and findings into publishable and promotable scientific processes and results.
Project Support
- Provide statistical expertise and guidance based on established methodologies throughout the project life cycle in the areas of study policies, protocols, implementation timelines and processes, data interpretation and publication of results.
- Work with data management team to ensure data captured incorporates and corresponds to project protocols and requirements.
Statistical Analysis/Data Collection Planning
- Prepare statistical analysis plan and oversee project data collection, management, and analysis with input from the project teams that incorporates the type of information collected, sample size, randomization procedures, table and listing shells, project statistical policies, protocols, and methodology to be used to appropriately translate scientific questions into statistical hypotheses.
Study Report Support
- Assist medical director(s) and/or technical writers by preparing statistical section of study report, publications and/or presentations ensuring statistical analyses adheres to trial, sponsor, organizational and regulatory requirements, and best practices.
Qualifications
- A minimum of a Bachelor's or Master's degree and a professional designation + 1-3 years of related experience.
Working Conditions
- Home-based.
$78,000 - $130,000 a year
+ Annual Bonus - Target 8%
Extended Health Benefits:
- Health
- Drug
- Dental
- Vision
- Out of Province/Country Emergency Health
Insurance & Protection:
- Accidental Death & Dismemberment (AD&D)
- Life Insurance for you and your family members
- Short- and Long-Term Disability
Retirement Savings:
- Group Retirement Savings Plan (7% employer match with 5% employee contribution)
Wellness & Lifestyle Perks:
- Education Reimbursement of up to $1,050 CAD (or local equivalent) annually for eligible expenses
- Summer Hours Program
- Work Abroad Program - enjoy up to 4 weeks per year of remote work outside your home region
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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