Find work in Canada.

621,374 jobs across our Canadian network. How we count

Jobs in Canada

25+ jobs

Email me new jobs Save this search

Added 6 mins ago
LC
Assistant Front Store Manager, Hourly Part Time Day
Loblaw Companies Limited
Oshawa, ON
- Part-time
Added 6 mins ago
LC
Cashier, Hourly Full Time Flexible Shifts
Loblaw Companies Limited
Brandon, MB
- Full-time
Added 6 mins ago
PC
HES Specialist – Canada (East Region)
Parkland Corporation
Quebec, QC
- Full-time
Added 6 mins ago
LC
Assistant Front Store Manager, Hourly Full Time Flexible Shifts
Loblaw Companies Limited
Oshawa, ON
- Full-time
Added 6 mins ago
HB
Senior Linux Platform Engineer - Trading Firm - $150,000-$350,000 CAD + Bonus
Hunter Bond
Montreal, QC
- $150,000 to $350,000 CAD / year
- Full-time
Added 6 mins ago
HB
Business Analyst / Project Manager – Corporate Applications / Salesforce / Workday - FinTech - $120,000-$200,000 CAD + Bonus
Hunter Bond
Montreal, QC
- $120,000 to $200,000 CAD / year
- Full-time
BA skills will be required for core responsibilities such as requirement gathering and project scoping.
Added 6 mins ago
LC
Merchandiser, Hourly Part Time Flexible Shifts
Loblaw Companies Limited
Ottawa, ON · Nepean, ON
- Part-time
Cash responsibilities (if applicable) require accuracy and efficiency in processing the customer order
Added 35 mins ago
TT
Maintenance Planner
Top Tier Talent Group
Gimli, MB
- Full-time
Added 35 mins ago
A
Electrical Technologist
Actalent
Toronto, ON · Etobicoke, ON
- $35 to $48 CAD / hour
- Full-time
Added 35 mins ago
P
Retail Operations Lead
PetSmart
Belleville, ON
- Full-time
Job responsibilities include, but are not limited to, the following and may vary depending on store characteristics and needs:
Added 35 mins ago
SD
Beauty Specialist, Hourly Part Time Flexible Shifts Greenlight Requisition
Shoppers Drug Mart
Toronto, ON
- Part-time
Added 35 mins ago
SD
Merchandiser, Hourly Part Time Flexible Shifts Greenlight Requisition
Shoppers Drug Mart
Toronto, ON
- Part-time
Cash responsibilities (if applicable) require accuracy and efficiency in processing the customer order
Added 35 mins ago
SD
Pharmacy Manager, Hourly Full Time Flexible Shifts
Shoppers Drug Mart
Saskatoon, SK
- Full-time
Added 35 mins ago
C
Line Cook
Cineplex
Barrie, ON
- Part-time
Performs additional responsibilities, although not detailed, as requested by the Chef, or Sous Chef.
Added 51 mins ago
A
Room Attendant (Part-Time)
AccorHotel
Ottawa, ON
- Part-time
Reporting to the Housekeeping Leadership Team, responsibilities and essential job functions include but are not limited to the following:
Added 51 mins ago
QK
community support worker
Qualicare, Kamloops
BC · Merritt, BC
- $20 to $23 CAD / hour
- Full-time
Added 1 hour ago
BC
Head of Operations
BIOAGRINEC CONSULTING & RECRUTEMENT
Canada
- Full-time
Added 1 hour ago
TH
Associé, Ventes, Électroménagers
The Home Depot Canada
Lethbridge, AB
- Part-time
Added 1 hour ago
TH
Lumber Sales Associate Part Time - 7170 Lethbridge
The Home Depot Canada
Lethbridge, AB
- Part-time
Added 1 hour ago
GE
Stage Bar Host
Grey Eagle Resort & Casino
Calgary, AB
- Full-time
…that safe work practices are adhered to at all time. Other responsibilities include assisting the FoH Manager, Supervisor(s), Servers and Cashiers in areas when and where…
Added 1 hour ago
GE
Bar Assistant - Stage Bar
Grey Eagle Resort & Casino
Calgary, AB
- Full-time
Added 1 hour ago
TH
Millwork Sales Associate Part Time - 7036 Medicine Hat
The Home Depot Canada
Medicine Hat, AB
- Part-time
Added 1 hour ago
GE
Blaze Bar & Grill Server
Grey Eagle Resort & Casino
Calgary, AB
- Full-time
Additional responsibilities include supporting the Outlet Supervisor and Front of House team in other operational areas as required.
Added 1 hour ago
GE
Buffet Host
Grey Eagle Resort & Casino
Calgary, AB
- Full-time
…that safe work practices are adhered to at all times. Other responsibilities include assisting the Front of the House Manager, Supervisor(s), Servers and Porters in areas when and where…
Added 1 hour ago
GE
Banquet Server
Grey Eagle Resort & Casino
Calgary, AB
- Full-time

AbbVie

Clinical Research Associate II

Oakville, ON, Canada

$81,000 to $131,000 CAD / year · Full-time

Apply About employer

Applications open in a new tab.

Job details

Pay: $81,000 to $131,000 CAD / year
Job type: Full-time
Apply by: Nov 19, 2026
Experience: Minimum of 2 years of clinically-related monitoring experience.
Posting language: English
Posted: Nov 4, 2026

Original job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Our Great Place to Work® Certification highlights our dedication to cultivating a high-trust, and inclusive culture for all.

At AbbVie, you won't just have a job, you’ll have the opportunity to unlock a bright future, because we're not just a workplace; we're a world of possibilities.

Difference makers wanted. Apply now!

What’s In It for You?

Innovative work culture
Professional development
Paid time off: vacation, holidays, personal days, and volunteer days
Employee stock purchase
Wellness spending account
Flexible health insurance
Retirement savings programs
Bonus plan

Job Description

To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of Clinical Site Management deliverables involving start-up, execution, and close-out of studies.

Key Responsibilities:

Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.
Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase I to III studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes.
Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites.
Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.
Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.
Manages investigator payments as per executed contract obligations. Negotiates investigator/ hospital agreements with stakeholders. Maintain and complete own expense reports as per local and applicable guidelines.
Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.

Qualifications

Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.
Minimum of 2 years of clinically-related monitoring experience. Experience in on-site monitoring of investigational drug or device trials is required.
Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
Familiarity with all aspects of study monitoring; data, drug accountability, documentation experience.
Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function.
Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.
Demonstrated business ethics and integrity.
A minimum of 50% travel is required.
Proficient with Microsoft Office Suite (Outlook, PowerPoint, Excel, Word, etc.)
Must be at ease with technology (the use of various tools/systems to perform day-to-day tasks).
Valid driver’s license and passport.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Workday Global Grade: 15

Compensation: CAD 81000 - CAD 131000 - yearly

Apply About employer

More about this job

Responsibilities

The Clinical Research Associate II monitors clinical investigative sites to ensure protocol adherence, regulatory compliance, and high-quality data submission. They also manage site activities, train personnel, and facilitate investigator payments while maintaining inspection readiness.

Requirements

Candidates must have at least 2 years of clinically-related monitoring experience and a tertiary qualification in a health-related field. Strong knowledge of ICH/GCP guidelines and the ability to travel at least 50% of the time are required.

Skills

Clinical monitoring
Protocol execution
GCP compliance
ICH guidelines
Site management
Regulatory inspection readiness
Data quality assurance
Safety event reporting
Investigator training
Contract negotiation
Analytical skills
Interpersonal communication
Microsoft Office Suite
Clinical research regulations
Drug accountability
Documentation

Benefits

Innovative work culture
Professional development
Paid time off
Employee stock purchase
Wellness spending account
Flexible health insurance
Retirement savings programs
Bonus plan

Visa sponsorship

Not detected in the job text

Keywords

Clinical Research Associate
Clinical Trials
Phase I-III
GCP
ICH Guidelines
SOPs
Site Monitoring
Protocol Execution
Regulatory Compliance
Investigational Drug
Data Management
Safety Reporting
Investigator Management
Clinical Site Management
R&D
Therapeutic Areas
Immunology
Oncology
Neuroscience
Allergan Aesthetics
Microsoft Office
Business Ethics
Travel
Clinical Research

Report this job