Full-time jobs in Canada

Explore full-time jobs across Canada. Choose a location and read the full job details.

340,510 listings · 45,233 employers Counted Nov 3, 2026. How we count

About these jobs

Employers hiring include Walmart Canada (8,164 listings), Health Match BC (2,995 listings), Walmart (2,620 listings).

Common roles: Cook, Project manager, Sales representative.

61,704 of these listings include employer-provided pay. Open a job to see its currency and pay period.

Advertised starting pay
Pay period	Median starting pay	Listings
CAD / hour	24.00	36,399
CAD / year	80,000.00	21,247
USD / year	98,576.50	1,488
USD / hour	20.00	617
CAD / month	5,027.00	611
CAD / week	1,445.00	51
CAD / day	375.00	37
USD / week	1,622.80	17
GBP / year	40,000.00	14
USD / month	4,000.00	13
EUR / year	65,000.00	11

Employer-listed minimums from at least 10 listings per currency and pay period. These are advertised starting amounts, not employee salaries. Jobs without a minimum and unusual amounts are excluded.

Workplace classifications: 2% remote, 16% hybrid, 82% on-site, 0% not specified. Hybrid and on-site classifications may be inferred from descriptions. Check the original ad.

Based on the dated count above. Listings can change. How we count

Full-time jobs in Canada

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Tech Observer

Senior Clinical Research Associate (Contract)

Canada

Full-time

Apply About employer

Applications open in a new tab.

Job details

Job type: Full-time
Posting language: English
Posted: Nov 2, 2026

Original job description

Tech Observer, a Global CRO with headquarters in New Jersey and offices in India, Denmark, the UK, and Singapore - along with an extended network across Brazil, Mexico, Australia, China, Malaysia, South Korea, Taiwan, Thailand, Vietnam, and more.

We are currently looking for Clinical Research Associates (CRAs)/ Senior CRA in Canada on contract.

PFB Job Responsibilities (But not limited to)

Manage and co-ordinate efforts of cross-functional project teams to support milestone achievement and to manage study issues and obstacles.

Ensure consistent use of study tools and training materials and compliance with standard processes, policies and procedures.

Arrange and participate in investigator meetings and liaise with vendors to facilitate the smooth conduct of the same.

Identify and manage vendors in accordance with Tech Observer/ Sponsor SOP’s, GCP and Local Regulatory Guidelines for study specific deliverables (including but not limited to; Clinical Trial Management System, Study Equipment’s, Travel Arrangements, Couriers, etc.) in delegated projects.

Develop study management plans and generate tools to facilitate tracking of performance at project level.

Serve as primary point of contact with Sponsor to ensure communication is maintained and reporting schedules are adhered to.

Identify quality issues within the study to implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties (Senior Management Tech-Observer/ Sponsor/ Data Management/ Medical Writing/ Stats, etc.).

Liaise with study team and facilitate (if required) selection of Investigator/ site as well as assist in Contract development and setting up the Investigator payment procedures for designated studies. In absence of team members, ensure the Investigator/ site payments are processed as per the agreed timelines in the executed contract.

Provide inputs for the development of proposals for new work and manage project budgets.

Provide input to line managers of their project team members’ performance relative to project tasks.

Prepare and present project information at internal and external meetings.

Participate in proposal development and in the bid-defence process with guidance and supervision.

Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site/visits and ongoing mentoring of CRA team.

Recruitment, retention, training, appraisal and supervision of clinical trial team members.

Ensure timely recruitment of trial participants with secure randomisation processes and subsequent efficient and effective data management.

Monitoring the trial progress to ensure compliance with and adherence to the project plan and to identify, evaluate and rectify issues of importance.

Actively participates in site payment runs and basic understanding regarding data input into tracking systems and analysis of site payments with supervision.

Based on Project requirements, act as Lead for on-site/ remote monitoring projects. Responsible to ensure that all the related activities delegated are conducted in compliance with Tech Observer/ Sponsor SOP’s, Monitoring Plan, GCP and Local Regulatory Guidelines.

Understand the requirements of the various controlling bodies, agencies and frameworks, guiding the project in conformance to those requirements and co-ordinating any necessary audit processes.

Liaise with the Trials Steering Committee; Data Monitoring and Ethics Committee with a particular view on compliance with Research Governance, Good Clinical Practice, Data Protection and Ethical Requirements.

Work with the Lead Principal Investigator to ensure that the trial is meeting its targets, is producing meaningful output and to predict and plan any changes that warrant requests to changes in protocol, funding or time.

Ensure timely update of project deliverables to sponsor representatives and key stake holders.

Organize and steer regular client update meetings and ensure timely provision of meeting minutes.

Oversee the creation and maintenance of all trial files, including the trial master file, regulatory binder and Investigator site files.

Other responsibilities as delegated by the management representative.

Apply About employer

More about this job

Responsibilities

Coordinate clinical trial teams and vendors, monitor study progress, and ensure compliance with sponsor procedures, Good Clinical Practice, and local regulations. Manage study deliverables, budgets, quality issues, site and investigator relationships, team performance, and communications with sponsors and stakeholders.

Requirements

The posting seeks a mid-senior Clinical Research Associate to lead or support on-site and remote monitoring projects and coordinate clinical trial activities. It emphasizes experience with clinical operations, regulatory and GCP compliance, team supervision, vendor and site management, and study reporting; no specific education requirement is stated.

Skills

Clinical Trial Monitoring
Clinical Project Management
Good Clinical Practice
Regulatory Compliance
Vendor Management
Study Management
Risk and Issue Management
Quality Management
Site Selection
Investigator Relations
Budget Management
Team Leadership
Clinical Trial Recruitment
Data Management
Trial Master File Management
Stakeholder Communication

Visa sponsorship

Not detected in the job text

Keywords

Clinical Research Associate
Clinical Trial
Clinical Trial Management System
Good Clinical Practice
Standard Operating Procedures
Local Regulatory Guidelines
Monitoring Plan
Investigator Meetings
Vendor Management
Study Management Plans
Sponsor Communication
Corrective Action Plans
Investigator Site Selection
Investigator Contracts
Site Payments
Project Budgets
Co-Monitoring
Clinical Team Training
Participant Recruitment
Randomization
Data Management
Research Governance
Data Protection
Ethics Requirements
Trial Steering Committee
Data Monitoring and Ethics Committee
Trial Master File
Regulatory Binder
Investigator Site Files

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