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Clinical Data Associate Jobs in Ontario (NOW HIRING)

Premier Research

Premier Research is looking for a Clinical Research Associate to join our Clinical Monitoring, Site ... Monitors (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and ...

Stem Health

Associate Medical Director

Toronto, ON · On-site

$230 - $320/hr

Position Summary The Associate Medical Director role at Stem Health sits at the intersection of ... Participate in the review of clinical outcomes data, safety indicators, and member experience ...

Align Technology, Inc.

... clinical and commercial excellence teams. It represents the voice of the customer in France and ... Define and track market performance KPIs, ensuring data-driven decision-making and continuous ...

HR à la carte

Development Associate

Toronto, ON · On-site

... clinical excellence, system coordination, and compassionate support to ensure every child with ... You will also maintain strong data integrity, support accurate reporting, and track performance ...

Jazz Pharmaceutical

Global Study Leader

Mississauga, ON · On-site

... support data query process. * Perform monitoring visit report review (as required). * Lead and ... Mentor and coach Global Study Managers (GSMs) Clinical Research Associates (CRAs), and Global Study ...

Posted today

DiaSorin

ASSOCIATE SCIENTIST I - AGS

Toronto, ON · On-site

Occasionally, assemble and present data to departmental, project, and cross-site teams * Contribute ... Clinical Affairs, Assay R&D, and Quality Assurance regarding priorities and timetables for ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Ontario

Clinical Data Associate information

See Ontario salary details

$16

$35

$63

How much do clinical data associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical data associate in Ontario is $35.09, according to ZipRecruiter salary data. Most workers in this role earn between $25.96 and $38.94 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs

What are the most commonly searched types of Clinical Data jobs in Ontario?

The most popular types of Clinical Data jobs in Ontario are:

What are popular job titles related to Clinical Data Associate jobs in Ontario?

For Clinical Data Associate jobs in Ontario, the most frequently searched job titles are:

What job categories do people searching Clinical Data Associate jobs in Ontario look for?

The top searched job categories for Clinical Data Associate jobs in Ontario are:

What cities in Ontario are hiring for Clinical Data Associate jobs?

Cities in Ontario with the most Clinical Data Associate job openings:

Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $72,991 per year, or $35.1 per hour.

Clinical Research Associate

Premier Research

On-site, Remote

Full-time

Medical, Life, Retirement, PTO

Posted 13 days ago

Job description

Premier Research is looking for a Clinical Research Associate to join our Clinical Monitoring, Site Management and SSU team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

  • We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.

  • Your ideas influence the way we work, and your voice matters here.

  • As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What You'll be Doing:

  • Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines

  • Maintains submission of expenses according to travel and expense requirements within company guidelines

  • Monitors (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations

  • Plans day to day activities for monitoring of a clinical study and sets priorities per site

  • Prepares for and conducts on-site qualification, study initiation, interim monitoring, and close-out monitoring visits at investigator sites as required by clinical monitoring plan

  • Maintains Trial Master File (TMF)/electronic Trial Master File (eTMF) as defined by the organization's processes per filing guidelines. Understands the required essential documents according to ICH/GCP Section 8.

  • Reviews site documents and verifies they are accurate, complete, current, and include required updates

What we are searching for:

  • Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required

  • Previous clinical research experience required to include at least 1 year of independent monitoring

  • Experience working ideally across all, if not some, of the following therapy areas; Neurology, Oncology, and Dermatology

  • Experience at supporting Phase II & III studies.

The role can be offered as fully remote and applications will ideally be based in central Poland.

Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The minimum annualized starting base pay for this role is 113,000 PLN. The actual salary will be influenced based on a variety of factors such as qualifications, skills, competencies, and proficiency for the role. We also offer comprehensive benefits packages, which may include health insurance, life insurance, retirement plan, paid time off, and an Employee Assistance Program.

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