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Added 6 mins ago
C
Journalist (English Services) (On-Site)
CBC/Radio-Canada
Moncton, NB
- Full-time
…rollout in news and current affairs, on all platforms, and on local, regional and national programming. You have the curiosity and competence to find and tell investigative stories in any…
Added 6 mins ago
C
Reporter/Editor (English Services) (On-Site)
CBC/Radio-Canada
Fredericton, NB · Saint John, NB · Corner Brook, NL · Gander, NL · St. John's, NL · Halifax, NS · Sydney, NS · Charlottetown, PE
- Full-time
…rollout in news and current affairs, on all platforms, and on local, regional and national programming. You have the curiosity and competence to find and tell investigative stories in any…
Added 6 mins ago
BT
Arborist Climbers - Canada
Bartlett Tree Experts
Nanaimo, BC
- Other
Responsible for carrying out other duties as assigned by the Crew Leader or designated supervisor, Arborist Representative, or Local Manager
Added 6 mins ago
BT
Arborist Climber
Bartlett Tree Experts
Ottawa, ON · Navan, ON
- Other
Performing ground, tree climbing, and aerial lift duties in support of specific job assignments, as directed by the Arborist Crew Leader and Local Manager
Added 6 mins ago
J
Legal Operations Associate (Remote)
Jerry.ai
Remote, Canada
- $65,000 to $80,000 USD / year
- Full-time
- Remote
The person who succeeds in this role is a natural driver: someone who owns their work from start to finish, solves complex problems without a manual, and has the grit to thrive in a startup…
Added 6 mins ago
A
Environmental Risk Assessor
AECOM
Burnaby, BC
- $57,000 to $75,000 CAD / year
- Full-time
Valid driver’s license and willingness to conduct fieldwork.
Added 6 mins ago
EG
Project Manager - Highways
Egis Group
Toronto, ON
- $130,000 to $180,000 CAD / year
- Full-time
…projects while building a career with global opportunities and local…
Added 7 mins ago
AT
Highway Driver
Armour Transportation Systems
Hanwell, NB
- Full-time
Armour Transportation Systems is currently seeking a professional and safety-focused Highway Driver based out of Fredericton, NB.This position is ideal for drivers who enjoy consistent…
Added 7 mins ago
RE
Director Business Development, Optimization - Power Producers
Rodan Energy Solutions Inc.
Mississauga, ON
- Full-time
Added 7 mins ago
BC
Intermediate Electrical Engineer
BBA Consultants
Thunder Bay, ON
- Full-time
Valid driver’s licence and willingness to travel for site work, inspections, commissioning and start-ups
Added 7 mins ago
Y
Internal Audit Specialist
YNCU
Kitchener, ON
- $67,000 to $71,000 USD / year
- Full-time
Must have a valid Ontario driver's licence and reliable available vehicle
Added 7 mins ago
BC
Intermediate Electrical Designer
BBA Consultants
Thunder Bay, ON
- Full-time
Valid driver’s licence and willingness to travel for site work, inspections, commissioning and start-ups
Added 21 mins ago
Sales Representative - Packaging & Facility Solutions
Imperial Brady
Blainville, QC
…Vancouver, British Columbia - ensuring efficient service and local support nationwide. We are incorporated in Canada, and our 100% Canadian leadership team ensures that decisions for Canada…
Added 21 mins ago
I.T.C. Infrastructure Technologist
City of Brandon
Brandon, MB
…the Collective Agreement between the City of Brandon and CUPE Local 69. First consideration will be given to current City of Brandon CUPE employees. The City of Brandon reserves the right…
Added 21 mins ago
IT Support Analyst (12 Month Contract)
Greenfield Global Inc.
Chatham-Kent, ON · Chatham, ON
Provide technical support and customer service to local and remote staff
Added 22 mins ago
MA
Nurse Practitioner - Nurse-Led Outreach Team - Temporary Full-Time (Multi-Site)
Muskoka Algonquin Healthcare
Huntsville, ON
- Full-time
…(LTC) Homes and staff, community organizations, physicians and local hospital staff to enhance the circle of care for complex residents and their families. In addition, the NP will provide…
Added 22 mins ago
U
Collingwood Driver Helper
UPS
Owen Sound, ON
- Part-time
Meet UPS driver at the assigned local meet point
Added 22 mins ago
U
Port Elgin Driver Helper
UPS
Owen Sound, ON
- Part-time
Meet UPS driver at the assigned local meet point
Added 22 mins ago
U
Port Elgin Driver Helper
UPS
Owen Sound, ON
- Part-time
Meet UPS driver at the assigned local meet point
Added 22 mins ago
U
Collingwood Driver Helper
UPS
Owen Sound, ON
- Part-time
Meet UPS driver at the assigned local meet point
Added 22 mins ago
VV
Field Service Technician
Veracity Ventures Inc.
AB · Alberta, Canada
- Full-time
Work Arrangement: This position is mainly based in Fort McMurray, AB location and requires local and overnight travel to customer sites in the greater region of Alberta.
Added 22 mins ago
CH
Route Driver/Service Rep (Class DZ)
Clean Harbors
Brampton, ON
- Full-time
Safety-Kleen, a Clean Harbors Company, in Brampton, ON is seeking a DZ Driver (Sales and Service Representative) to join their safety conscious team! The SSR will be responsible for both…
Added 22 mins ago
CC
Parts Delivery Driver / Warehouse Associate
Crane Carrier (Canada) Limited
Cambridge, ON
- Full-time
Deliver parts to local customers within the market and record sales/delivery information
Added 37 mins ago
NP
Program Assistant (PA-1126-T)
New Path Youth and Family Services
Barrie, ON
- Full-time
Willingness to travel to other agency offices using personal vehicle. Must have a valid driver's license with minimum G2.
Added 37 mins ago
Q
Field Inspector
Quiktrak
Windsor, ON
- Contract
Quiktrak is seeking Audit and Inventory Inspectors to perform field audit inspections in your local area. As an independent contractor, you will travel to assigned locations to perform…

AbbVie

Clinical Research Associate II

Oakville, ON, Canada

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

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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

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