Jobs in Milton, ON and nearby (32,070 jobs)

Jobs within 25 km of Milton, ON, Canada. Nearby towns and cities are included. Distances are straight-line, not driving distances.

32,070 listings · 5,134 employers Counted Nov 11, 2026. How we count

About these jobs

Employers hiring include Loblaw Companies Limited (856 listings), Shoppers Drug Mart (670 listings), Walmart Canada (636 listings).

Common roles: Retail sales associate, Project manager, Sales representative.

5,703 of these listings include employer-provided pay. Open a job to see its currency and pay period.

Advertised starting pay
Pay period	Median starting pay	Listings
CAD / hour	26.00	2,976
CAD / year	80,000.00	2,552
CAD / month	3,200.00	13

Employer-listed minimums from at least 10 listings per currency and pay period. These are advertised starting amounts, not employee salaries. Jobs without a minimum and unusual amounts are excluded.

Workplace classifications: 0% remote, 18% hybrid, 82% on-site, 0% not specified. Hybrid and on-site classifications may be inferred from descriptions. Check the original ad.

Based on the dated count above. Listings can change. How we count

Jobs in Milton, ON and nearby

Within 25 km

Group jobs by employerEmail me new jobs Save this search

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ICON plc

Associate Clinical System Designer

Burlington, ON, Canada
Canada, Burlington, Canada

Full-time

Apply on icon.wd3.myworkdayjobs.com About employer

Applications open in a new tab.

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 Milton, ON and nearby