Jobs in Canada

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Added 1 hour ago
J
Senior Clinical Trial Manager (Sr CTM), Dermatology & Rheumatology
Jobgether
Canada
- Full-time
The Senior Clinical Trial Manager will oversee clinical trial operations and monitoring activities across dermatology and rheumatology studies, ensuring high-quality delivery and compliance…
Added 3 hours ago
TU
Research Associate
The University of British Columbia
Kelowna, BC
- Full-time
The Research Associate develops collaborations across both UBC campuses, including the Michael Smith Laboratories (MSL), and with clinical, government and industry partners. Working with…
Added 5 hours ago
H
Clinical Research Site Supervisor
HealthCareersInSask.ca
Regina, SK
- Full-time
The Clinical Research Site Supervisor is actively involved in supporting quality assurance and quality improvement activities in the department, which would include; monitoring compliance…
Added 7 hours ago
UO
Research Associate
University of British Columbia
Kelowna, BC · UBCO | Engineering, Management and Education Building (EME)
- Full-time
The Research Associate develops collaborations across both UBC campuses, including the Michael Smith Laboratories (MSL), and with clinical, government and industry partners. Working with…
Added 12 hours ago
I
Consultant, Services de conseil et d’analyse / Consultant, Consulting & Analytics Services
IQVIA
Mississauga, ON · Montreal, QC · Quebec, QC
- Full-time
Participer à des interactions clients (p. ex., appels, ateliers) pour clarifier les besoins, tester des hypothèses et expliquer les méthodes, avec soutien de l’équipe senior.
Added 12 hours ago
Research Associate (Limited Term, 2 years)
University of Toronto
Toronto, ON
The Research Associate will serve as a senior scientific leader within the lab and will work in close partnership with Dr. Bowen Li (Principal Investigator) to oversee and advance the lab’s…
Added 21 hours ago
Associate Principal/Strategy & Medical Affairs (Life Sciences)
Charles River Associates - Private
Toronto, ON
…organizations, and advocacy groups from the earliest stages of research into new therapy areas, through clinical development, to the launch of therapies that will achieve commercial success…
Added 22 hours ago
UO
Senior Advisor, Executive Operations
University of Ottawa
Ottawa, ON · Roger Guindon Hall
- Full-time
…supported in carrying out institutional, Faculty, academic, research, clinical partnership and external leadership responsibilities. Establishes and maintains effective communication…
Added 1 day ago
UH
Technical Specialist
University Health Network
Toronto, ON
- Full-time
The Technical Specialist work closely with other Business Intelligence (BI) Analyst and Developer, Data Engineers, Clinical/SME teams and Other Epic Application Team, this position is…
Added 1 day ago
UH
Project Coordinator I - Peter Munk Cardiac Centre - Quality Registry
University Health Network
Toronto, ON
- Full-time
…Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international…
Added 1 day ago
UH
Project Coordinator I - Peter Munk Cardiac Centre - Quality Registry
University Health Network
Toronto, ON
- Full-time
…Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international…
Added 2 days ago
IP
Associate Clinical System Designer
ICON plc
Burlington, ON · Canada, Burlington
- Full-time
Associate Clinical System Designer - United States, Canada, Mexico, Colombia
Added 2 days ago
P(
Associate Creative Strategist
Phoenix (YC W21)
Toronto, ON
- $70,000 to $80,000 CAD / year
- Full-time
We’re looking for an Associate Creative Strategist to help us scale performance creative across both of our brands, Phoenix and Raven. This is a hands-on, apprenticeship-style role for…
Added 2 days ago
I
Directeur adjoint, Solutions et pres associée, Stratégie des solutions et prestation (SDL) / Associate Director, Solution and Delivery Lead (SDL)
IQVIA
Toronto, ON
- Full-time
The Associate Director, Solution and Delivery Lead (SDL) serves as a strategic, scientific, and delivery leader within Real World Evidence (RWE) Solutions. This role is accountable for…
Added 2 days ago
IS
Clinical Research Associate 3
ICON Strategic Solutions
Canada
- Full-time
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Added 2 days ago
PC
Senior Clinical Research Associate
PSI CRO
Calgary, AB
- $120,000 to $150,000 CAD / year
- Full-time
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality…
Added 3 days ago
SH
Skin Wellness Associate Nurse
SE Health
Mississauga, ON
- Full-time
…the way we do our work. As a social enterprise, we support research into Senior’s Health and…
Added 3 days ago
TU
Senior Research Analyst, Pharmacoepidemiology
The University of British Columbia
Victoria, BC
- $8,087.08 to $12,117.08 CAD / month
- Full-time
The Senior Research Analyst will manage a team of research analysts and data analysts to perform pharmacoepidemiology studies for the BC Ministry of Health (MoH), Canadian Network for…
Added 3 days ago
P
Associate Creative Strategist
Phoenix
Toronto, ON
- $70,000 to $80,000 CAD / year
- Full-time
We’re looking for an Associate Creative Strategist to help us scale performance creative across both of our brands, Phoenix and Raven. This is a hands-on, apprenticeship-style role for…
Added 3 days ago
UO
Senior Research Analyst, Pharmacoepidemiology
University of British Columbia
Victoria, BC · BOFF | Therapeutics Initiative (THRPI)
- $8,087.08 to $12,117.08 CAD / month
- Full-time
The Senior Research Analyst will manage a team of research analysts and data analysts to perform pharmacoepidemiology studies for the BC Ministry of Health (MoH), Canadian Network for…
Added 3 days ago
AP
Senior Medical Science Liaison Hematology/Oncology (Ontario West/Manitoba)
Astellas Pharma
Markham, ON
- Full-time
Astellas Canada – Senior Medical Science Liaison Hematology/Oncology (Ontario West/Manitoba)
Added 3 days ago
Scientific Director - Geriatric Division Research
CAMH
Toronto, ON
As Canada’s leading mental illness research facility, CAMH’s Campbell Family Mental Health Research Institute (CFMHRI) is home to scientists, staff and research trainees conducting leading…
Added 3 days ago
QU
Faculty Resource & Compensation Coordinator (J0926-0129)
Queen's University
Kingston, ON
- $62,142 to $75,772 CAD / year
- Full-time
Reporting to the Associate Director, Administration, Initiatives, and Operations (AIO), the Faculty Support Coordinator performs a broad range of complex administrative, operational, and…
Added 3 days ago
Associate Director of Programs - Wellbrook Place West
Partners Community Health
Mississauga, ON
Identify service gaps and emerging resident needs, and lead the design of new or enhanced programs in collaboration with clinical and interdisciplinary teams.
Added 3 days ago
ASSOCIATE SCIENTIST I - AGS
DiaSorin
Toronto, ON
Participate in the Company's day-to-day Research and Development activities which include: design, execution and interpretation of scientific experiments and design and development of…

ICON plc

Associate Clinical System Designer

Burlington, ON, Canada
Canada, Burlington, Canada

Full-time

Apply on icon.wd3.myworkdayjobs.com About employer

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Job details

Job type: Full-time
Posting language: English
Posted: Nov 10, 2026

Original job description

Associate Clinical System Designer - United States, Canada, Mexico, Colombia

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking an Associate Clinical System Designer to join ICON’s Full-Service IOD Clinical Data Science team. As an Associate Clinical System Designer at ICON, you will play a pivotal role in designing and implementing advanced clinical systems that enhance trial design and execution.

Locations:

Mexico City (Office-Based Hybrid)
Blue Bell, USA (Office-Based Hybrid)
Raleigh, NC (Office-Based Hybrid)
Colombia (Remote)
Canada (Remote)

What you will be doing:

Assist with development of Custom CRF screens, Edit Check, and Dynamic Check specification documents, using prototyping methodologies as needed
Assist with the creation of technical specifications for output programming such as Data Validation Outputs, Data Analytics outputs, custom output programs etc.
Copies and modifies CRFs from standard libraries and other studies under specific instruction
Read, ensure understanding and adhere to the study protocol, contract and scope of work for all tasks during set-up, maintenance and close-out of the study
Tracks and keeps functional management and those responsible for project management informed of any issues that might affect project target dates, scope or budget and escalates potential problems effectively and in a timely manner
With support, consolidates and completes the high-level system requirements documents and facilitates their review
With support, performs quality control peer reviews of database related specifications as needed and records comments appropriately
Supports more senior project leads in performing eCRF and other specification review meetings
Supports for simple to medium migration/post-production change activities
Assist with the EDC integration related activities

Your profile:

6+ months of experience in the design and implementation of clinical systems within the clinical research industry
Expertise in data analysis and interpretation or Database Development, with proficiency in clinical data management systems and software
Experience with Medidata Rave and/or Veeva EDC
Functional knowledge of CRF design tools and ability to plan and design CDMS components directly from interpretation of medium complexity clinical trial protocols
Excellent written and verbal communication skills
Bachelor’s Degree in a relevant field

Please submit all applications in English *

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Apply on icon.wd3.myworkdayjobs.com About employer

More about this job

Responsibilities

The Associate Clinical System Designer will assist in the design and implementation of clinical systems, including CRF screens and edit checks. They will also support technical specification creation and ensure adherence to study protocols throughout the trial lifecycle.

Requirements

Candidates must have at least 6 months of experience in clinical system design within the clinical research industry. A Bachelor's degree in a relevant field and proficiency with EDC software like Medidata Rave or Veeva are required.

Skills

Clinical system design
Data analysis
Database development
Clinical data management systems
Medidata Rave
Veeva EDC
CRF design
Technical specifications
Data validation
Clinical trial protocols
Communication skills
Quality control
Prototyping

Benefits

Competitive base salary
Performance related incentives
Medical coverage
Dental coverage
Vision coverage
Retirement plans
Pension plans
Life assurance
Disability coverage
Employee assistance programmes
Wellbeing resources
Learning and development opportunities

Visa sponsorship

Not detected in the job text

Keywords

Clinical Research
Clinical Data Science
CRF
eCRF
EDC
Medidata Rave
Veeva EDC
Clinical Trial
Data Validation
Database Development
Protocol
System Requirements
Clinical Systems
Data Analytics
Healthcare Intelligence

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Work requirements

Jobs in Canada