Find work in Canada.

A simpler way to find your next job.

Jobs in Canada

25+ jobs

Email me new jobs Save this search

Added 5 mins ago
N
Material Handler
Napoleon
Barrie, ON
- Full-time
Appreciation events, raffles, and team building activities
Added 5 mins ago
FN
Mortgage Underwriter, Excalibur
First National Financial LP
Vancouver, BC
- Full-time
Internal: Associate Mortgage Underwriters and Funders
Added 5 mins ago
WS
Team Leader - 24 Afternoons
Wolf Steel Ltd
Barrie, ON
- Full-time
Appreciation events, raffles, and team building activities
Added 20 mins ago
R
Associate Director - Operational Excellence - Client Lifecycle Management (CLM)
RBC
Toronto, ON
- Full-time
The Operational Excellence Associate Director drives execution of audit remediation activities and operational excellence initiatives within the Client Lifecycle Management pillar. This…
Added 20 mins ago
D|
Quality Assurance Compliance Associate (Contract)
DECIEM | THE ABNORMAL BEAUTY COMPANY
Toronto, ON · Etobicoke, ON
- Contract
We’re hiring a Quality Assurance Compliance Associate tofacilitate the transition of day-to-day execution, including the management of NCRs, CAPAs, LIRs, routine eQMS administration, and…
Added 20 mins ago
F
Fulfillment Associate- 1st Shift (Monday to Friday, Days)
FYUL
Mississauga, ON
- Full-time
…That’s why we’re looking for a detail-oriented Fulfillment Associate to join us. In this position, you’ll assist with our printing, shipping, packing, and other fulfillment needs, and…
Added 20 mins ago
F
Fulfillment Associate- 2nd Shift (Monday to Friday, Afternoons)
FYUL
Mississauga, ON
- Full-time
…That’s why we’re looking for a detail-oriented Fulfillment Associate to join us. In this position, you’ll assist with our printing, shipping, packing, and other fulfillment needs, and…
Added 50 mins ago
BL
Manager, Student Programs & Professional Development
BC Legal Management Association
Vancouver, BC
- Other
…professional development of summer and articling students, student events and liaising with law schools. You will work closely with our Director, Professional Development and Marketing on…
Added 50 mins ago
SD
Beauty Manager, Hourly Full Time Flexible Shifts
Shoppers Drug Mart
Grand Bend, ON
- Full-time
Books appointments for events and manages annual incremental event schedule
Added 50 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.
Added 50 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.
Added 50 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.
Added 50 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.
Added 50 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.
Added 50 mins ago
EE
Employment Specialist
Express Employment Professionals - Calgary
Calgary, AB
- Full-time
Participate in client visits, safety tours, and marketing events.
Added 1 hour ago
N
Team Leader - 24 Afternoons
Napoleon
Barrie, ON
- Full-time
Appreciation events, raffles, and team building activities
Added 1 hour ago
A
Clinical Research Associate II
AbbVie
Oakville, ON
- $81,000 to $131,000 CAD / year
- Full-time
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.
Added 1 hour ago
HE
Entry level Marketing Associate
Hype Events
Toronto, ON · Greater Toronto Area, Canada
- $41,000 to $45,000 CAD / year
- Full-time
We bring brands to life through face-to-face marketing, promotional events, and customer engagement campaigns. We help our clients connect with their audiences through real conversations,…
Added 1 hour ago
GW
Associate Lawyer - Lending
Gowling WLG
Toronto, ON
- Full-time
Gowling WLG’s Toronto office is currently seeking a motivated Associate with 2-5 years of post-call Lending experience with a recognized law firm to join its Lending Group. The successful…
Added 1 hour ago
TO
Financial Sales Manager II Target
Top of Virginia Regional Chamber
Winchester, ON
- Full-time
…authorities, providing one on one feedback and coaching that supports associate development and achievement of results. Regularly and proactively leverage the expertise of bank partners,…
Added 2 hours ago
NS
Family Medicine-Family Physician Clinician Scientist & Practitioner-Sydney-Cape Breton Medical Campus
Nova Scotia Healthcare System
Sydney, NS
- Full-time
Report to the Senior Associate Dean at the CBMC.
Added 2 hours ago
MR
Associate Lawyer
Meridia Recruitment Solutions, a KBRS Company
Halifax, NS
- Full-time
…boutique litigation firm based in downtown Halifax, to recruit an Associate Lawyer, Insurance Defence Litigation. Focused on insurance defence and marine law, Ritch Williams & Richards…
Added 2 hours ago
C
Sales Development Representative
Carousel
Montreal, QC
- Full-time
Sales Development Representative (Associate Level)
Added 2 hours ago
SD
Beauty Specialist, Hourly Part Time Day Greenlight Requisition
Shoppers Drug Mart
St. John's, NL
- Part-time
Actively promote and book appointments for in-Store events
Added 3 hours ago
SD
Beauty Specialist, Hourly Part Time Evening Greenlight Requisition
Shoppers Drug Mart
Toronto, ON
- Part-time
Actively promote and book appointments for in-Store events

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