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Clinical Data Associate Jobs in Alberta (NOW HIRING)

destinationone Consulting

Radiology Nurse

Calgary, AB · On-site

We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Associate's or Bachelor's). Experience in radiology or related field preferred. Strong clinical ...

destinationone Consulting

We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Associate's or Bachelor's). Experience in radiology or related field preferred. Strong clinical ...

Rochester Regional Health

CA$38.66 - CA$51.91/hr

... clinical care * Performs initial and ongoing assessment of the patient, utilizing appropriate data ... Diploma or Associate's Degree in Nursing * Registered Nurse license in New York State. * Basic Life ...

Rochester Regional Health

CA$38.66 - CA$51.91/hr

... clinical care * Performs initial and ongoing assessment of the patient, utilizing appropriate data ... Diploma or Associate's Degree in Nursing * Registered Nurse license in New York State. * Basic Life ...

Rochester Regional Health

CA$38.66 - CA$51.91/hr

... clinical care * Performs initial and ongoing assessment of the patient, utilizing appropriate data ... Diploma or Associate's Degree in Nursing * Registered Nurse license in New York State. * Basic Life ...

Rochester Regional Health

CA$38.66 - CA$51.91/hr

... clinical care * Performs initial and ongoing assessment of the patient, utilizing appropriate data ... Diploma or Associate's Degree in Nursing * Registered Nurse license in New York State. * Basic Life ...

Rochester Regional Health

CA$38.66 - CA$51.91/hr

... clinical care * Performs initial and ongoing assessment of the patient, utilizing appropriate data ... Diploma or Associate's Degree in Nursing * Registered Nurse license in New York State. * Basic Life ...

destinationone Consulting

We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Strong clinical assessment and critical thinking skills to respond effectively to emergencies.

destinationone Consulting

We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Strong clinical skills and a thorough understanding of pediatric healthcare. Excellent ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Alberta

Clinical Data Associate information

See Alberta salary details

$16

$35

$63

How much do clinical data associate jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical data associate in Alberta 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 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 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 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 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 Alberta? The most popular types of Clinical Data jobs in Alberta are:
What are popular job titles related to Clinical Data Associate jobs in Alberta? For Clinical Data Associate jobs in Alberta, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate jobs in Alberta look for? The top searched job categories for Clinical Data Associate jobs in Alberta are:
Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Alberta as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $72,991 per year, or $35.1 per hour.

Bilingual Sr. Clinical Research Associate

Alimentiv

Calgary, AB • Remote

Full-time

Re-posted 10 days ago

Job description

Positions available: 1 (remote based, Canada)
Must be fluent in English and French
 
Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale.  In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document management, monitoring project site budgets and regulatory filings that aligns with SOPs, study guidelines and GCP best practices.  In the function of Lead CRA, will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans, protocols, CRFs, communications or other monitoring forms, documents and tools. Represents the corporation by maintaining collaborative relationships with stakeholders.
 
 
Monitoring - Subject Expert
  • Act as subject matter expert, mentor, coach and/or provide performance feedback to manager for peers.
  • Assist with selection, hiring, training, and supervision of CRAs as needed. Perform co-monitoring and training visits with CRAs. 
  • When required, act as the first escalation point for the resolution of site/patient issues or to address Sponsor concerns.
  • May represent Director, Monitoring and Site Management or Manager, Clinical Site Management in BD initiatives with a site monitoring focus.
Project Monitoring Lead
  • May be assigned Lead CRA role and manage monitoring services for a group of projects and/or CRAs on large/complex project(s) including directing/guiding day to day activities and review/approval of monitoring reports.
  • Function as liaison between CRAs and other functional teams, escalating concerns and issues to management as needed.
  • Participate and/or present at study team, kickoff and investigator meetings and act as primary contact to sponsors for all monitoring related issues.
Site Recruitment and Setup
  • Identify and recruit site investigators, coordinate the movement and delivery of trial materials, samples, tests and forms, including investigational product, protocols, SOPs, CRFs, project documents, forms and support tools.
  • Ensure SOPs in place to optimize patient recruitment providing guidance to site teams of inclusion/exclusion criteria.
Investigational Site Monitoring
  • Primary clinical site contact.
  • May act as primary contact for any questions or issues that arise from investigational sites.
  • Oversee overall integrity of the study to promote positive working relationships with the site and staff.
  • Facilitate and support site staff with access to study systems and ensure sites are compliant with project specific training requirements.
  • Ensure all site related issues are followed until resolution.
  • Coordinate delivery of clinical sites communications, collaborating with project teams, to ensure investigational sites are provided accurate ongoing data, updates, information and feedback on project/regulatory guidelines and objectives throughout the project lifecycle.
Qualifications
  • The successful candidate will possess a minimum of a college diploma/degree and 4-6 years of related experience.
  • Self-motivation with strong communication skills and a commitment to achieving positive results. 
  • Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results. 
  • Critical thinking abilities
  • Ability to regularly travel to sites.
Working Conditions
  • Home-based
  • Regular travel is required
$78,000 - $130,000 a year
+bonus
Stay Alert to Recruitment Scams
We have been made aware of individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process. Official communication will only come from our company email domains. If something doesn't feel right, we encourage you to verify before responding.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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