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Added 2 mins ago
Operations Test Engineering, Mechanical Tooling Co-Op (Waterdown, CAN)
L3Harris Technologies
ON · Waterdown, ON
…Intern is to assist for the concept, prototyping, design, and development of mechanical tooling to support the manufacturing build processes. This role will interface with the design teams,…
Added 2 mins ago
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Application must be received by October 14th , 2026 at 4:30PM.
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Manager, Human Resources | Gestionnaire, Ressources humaines
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Coach and advise leaders on people management practices, including performance management, feedback, and employee development
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Product Director, Mobile | Directeur ou directrice de produit, Mobile
NBCUniversal
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Champion the mobile experience throughout the development lifecycle, ensuring it is represented in planning, development, and delivery decisions.
Added 2 mins ago
H&M Sales Advisor
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Participate in relevant available Onboarding, introduction processes & trainings and courses relevant for your role & future development
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H&M Sales Advisor
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Participate in relevant available Onboarding, introduction processes & trainings and courses relevant for your role & future development
Added 16 mins ago
Entry-Level English Teacher (ESL) | Visa Sponsored
English 1
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Full-time
TEFL certification + skill development & career advancement
Added 16 mins ago
Manager, National Tax Services
ACCA Careers
Winnipeg, MB
Full-time
This bilingual opportunity is also available on MNP’s Postes avec expérience job board in French. Please submit one application only to be considered for this opportunity. Thank you.
Added 16 mins ago
Speech Language Pathologist Masters
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Technical Delivery Manager
Intelex Technologies ULC
Canada
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Since 1992, Intelex Technologies, ULC. is a global leader in the development and support of software solutions for Environment, Health, Safety and
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Logistics Support Engineer
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Toronto, ON
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Supervisor, Mine Operations (Construction Shaft)
Alamos Gold Inc.
Matachewan, ON
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…in Canada and one in Mexico – and have a strong portfolio of development-stage projects, including the Lynn Lake Project and Island Gold Phase 3+ Expansion in Canada, and the Puerto Del…
Added 16 mins ago
Mobile Maintenance Senior Supervisor
Alamos Gold Inc.
Matachewan, ON
Full-time
…Canada and one in Mexico – and we have a strong portfolio of development stage projects, including the Lynn Lake Project and Island Gold Phase 3+ Expansion in Canada, and Puerto Del Aire…
Added 16 mins ago
Senior Python & SQL Developer
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Montreal, QC
Full-time
Minimum 8+ years of experience in Python application development and SQL programming.
Added 16 mins ago
Samsung Home Electronics Sales and Product Specialist
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…employees to innovate and expand new horizons, making internal development our cornerstone. Find your place at Premium – whether it’s merchandising, sales or brand advocacy, there's a spot…
Added 16 mins ago
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Added 16 mins ago
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Jobgether

Senior Clinical Research Associate

Canada

Job type: Full-time
Posting language: English
Posted: Sep 30, 2026

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Original job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical Research Associate based in Canada.

This role offers the opportunity to contribute to clinical studies across a range of therapeutic areas while maintaining rigorous quality and compliance standards. You will take ownership of key monitoring activities, from site initiation and routine monitoring through close-out visits. The position combines on-site clinical monitoring with strong collaboration across study teams, support functions, vendors, and research sites. You will play an important role in site communication, data quality, regulatory preparation, and study progress tracking. The environment encourages continuous development and provides exposure to different clinical research programs and therapeutic indications. This is an opportunity for an experienced clinical research professional to deepen their expertise and broaden their experience across Phase II and III studies.

Accountabilities

Conduct and document Site Initiation Visits (SIV), Routine Monitoring Visits (RMV), and Close-Out Visits (COV) at clinical research sites.
Perform Case Report Form (CRF) review, source document verification, and query resolution to ensure data quality and protocol compliance.
Manage ongoing communication with assigned clinical sites and support effective site management throughout the study lifecycle.
Serve as a key point of contact for in-house support functions and external vendors involved in study activities.
Communicate regularly with internal project teams regarding site performance, study progress, and emerging issues.
Participate in feasibility activities to assess potential research sites and support study planning.
Assist regulatory teams with the preparation of documentation required for study submissions.
Prepare for and participate in clinical audits and regulatory inspections.
Contribute to maintaining high-quality study execution while ensuring applicable protocols, procedures, and regulatory requirements are followed.

Requirements

College or university degree in Life Sciences or an equivalent combination of education, training, and relevant experience.
Demonstrated independent on-site clinical monitoring experience.
Experience conducting different types of monitoring visits for Phase II and/or Phase III clinical studies.
Oncology clinical research experience is considered an asset.
Full professional proficiency in both English and French is essential.
Proficiency with Microsoft Office applications.
Strong planning and organizational skills, with the ability to manage multiple priorities in a dynamic team environment.
Excellent communication, collaboration, problem-solving, and interpersonal skills.
Ability and willingness to travel regularly for on-site monitoring activities.
Valid driver's license.

Benefits

Opportunity to work across a variety of clinical studies and therapeutic indications.
Exposure to different phases of clinical research, including Phase II and Phase III studies.
Opportunity to further develop clinical monitoring and research expertise.
Ability to broaden therapeutic area experience and build long-term expertise in clinical research.
Dynamic environment combining independent responsibilities with collaboration across clinical project teams.
Opportunity to contribute to high-quality clinical research while supporting study delivery and regulatory compliance.

How Jobgether Works

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

Why Apply Through Jobgether?

Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.

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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More about this job

Responsibilities

Conduct and document site initiation, routine monitoring, and close-out visits, while reviewing clinical trial data, resolving queries, and supporting site management. Coordinate with research sites, vendors, support functions, and project teams; contribute to feasibility, regulatory preparation, audits, inspections, and compliant study delivery.

Requirements

Requires a college or university degree in Life Sciences or equivalent education and experience, plus independent on-site monitoring experience in Phase II and/or Phase III studies. Candidates must be professionally proficient in English and French, skilled with Microsoft Office, organized and collaborative, and willing to travel regularly with a valid driver's license; oncology experience is an asset.

Skills

Clinical Site Monitoring
Site Initiation Visits
Routine Monitoring Visits
Close-Out Visits
Case Report Form Review
Source Document Verification
Query Resolution
Site Management
Clinical Trial Feasibility
Regulatory Documentation
Audit and Inspection Preparation
Protocol Compliance
Data Quality
Project Team Communication
Microsoft Office
English and French Proficiency

Benefits

Exposure to a variety of clinical studies and therapeutic indications
Professional development
Opportunity to broaden therapeutic area experience
Collaborative work environment

Visa sponsorship

Not detected in the job text

Keywords

Clinical Research
Clinical Trials
Clinical Site Monitoring
Site Initiation Visits
Routine Monitoring Visits
Close-Out Visits
Case Report Forms
Source Document Verification
Query Resolution
Site Management
Phase II Studies
Phase III Studies
Oncology
Clinical Trial Feasibility
Regulatory Submissions
Clinical Audits
Regulatory Inspections
Protocol Compliance
Data Quality
Study Progress Tracking
Vendor Coordination
Microsoft Office
Life Sciences
English
French

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