We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Strong clinical skills, critical thinking abilities, and excellent interpersonal communication ...
We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Strong clinical skills, critical thinking abilities, and excellent interpersonal communication ...
We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Strong clinical assessment and critical thinking skills to manage diverse patient needs in a home ...
We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Strong clinical assessment and critical thinking skills to manage diverse patient needs in a home ...
We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Strong clinical assessment and critical thinking skills to manage diverse patient needs in a home ...
We are proactively building a data bank for opportunities in these fields. By applying, you ensure ... Strong clinical assessment and critical thinking skills to manage diverse patient needs in a home ...
Spiritual Care Coordinator (2025-1548)
Calgary, AB · On-site
CA$33.64 - CA$44.15/hr
... of Clinical Pastoral Education (CPE). - Member or Associate Member in Good Standing with the ... If you would like more information about how your data is processed, please contact us. apply for ...
Spiritual Care Coordinator (2025-1548)
Calgary, AB · On-site
CA$33.64 - CA$44.15/hr
... of Clinical Pastoral Education (CPE). - Member or Associate Member in Good Standing with the ... If you would like more information about how your data is processed, please contact us. apply for ...
Case Manager II
Wildwood, AB · On-site
... your clinical expertise while contributing to the well-being of individuals in your community ... Participate in utilization review process: data collection, trend review, and resolution actions.
Case Manager II
Wildwood, AB · On-site
... your clinical expertise while contributing to the well-being of individuals in your community ... Participate in utilization review process: data collection, trend review, and resolution actions.
Clinical Data Associate information
See Alberta salary details
$16.35 - $20.67
9% of jobs
$20.67 - $25
13% of jobs
$26.01 is the 25th percentile. Wages below this are outliers.
$25 - $29.33
16% of jobs
The median wage is $33.65 / hr.
$29.33 - $33.65
13% of jobs
$37.56 is the 75th percentile. Wages above this are outliers.
$33.65 - $37.98
28% of jobs
$37.98 - $42.31
12% of jobs
$42.31 - $46.63
2% of jobs
$46.63 - $50.96
3% of jobs
$50.96 - $55.29
1% of jobs
$55.29 - $59.62
2% of jobs
$59.62 - $63.94
2% of jobs
$16
$35
$63
How much do clinical data associate jobs pay per hour?
As of Jul 16, 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.
Which is better, CDM or SAS?
For a Clinical Data Associate, SAS is a widely used software for data analysis and reporting in clinical trials, while CDM (Clinical Data Management) refers to the overall process of collecting, cleaning, and managing clinical data, often using various tools including SAS. SAS skills are highly valued in the role, but understanding the broader CDM process is also important for effective data handling and compliance.
What's next after CRC?
After working as a Clinical Research Coordinator (CRC), professionals often advance to roles such as Clinical Data Associate, Clinical Trial Manager, or Regulatory Affairs Specialist. Gaining experience, certifications like CCRP, and developing skills in data management and regulatory compliance can facilitate career progression in clinical research.
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 is the role of a clinical data associate?
A clinical data associate is responsible for collecting, managing, and ensuring the accuracy of data from clinical trials. They review data for completeness, resolve discrepancies, and use database tools to support data integrity and regulatory compliance throughout the trial process.
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.
Do you need a degree to be a CRC?
A Clinical Data Associate (CDA) typically does not require a specific degree, but a background in life sciences, healthcare, or related fields is often preferred. Many employers value relevant certifications and experience with clinical data management tools. Educational requirements can vary by employer and job level.
Is CRA an entry level job?
A Clinical Data Associate (CDA) role is typically considered an entry-level position in clinical research, often requiring a bachelor's degree in a related field and some familiarity with data management tools. However, a Clinical Research Associate (CRA) role usually requires more experience and is considered a mid- to senior-level position, involving site monitoring and regulatory compliance. Entry-level roles may serve as a stepping stone toward CRA positions with additional experience and certifications.
What is the difference between Clinical Data Associate vs Clinical Research Coordinator?
| Aspect | Clinical Data Associate | Clinical Research Coordinator |
|---|---|---|
| Primary Role | Manage and ensure accuracy of clinical trial data | Oversee trial operations, patient recruitment, and site management |
| Credentials | Bachelor's in life sciences or related field; familiarity with data management | Bachelor's in health sciences or related field; clinical trial experience |
| Work Environment | Data management teams, clinical trial databases | Clinical sites, hospitals, research facilities |
| Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, 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 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:
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Re-posted 3 days ago
Job description
destinationone Consulting specializes in recruitment across diverse sectors, including Healthcare, Health Tech, Government, Municipalities, Non-Profits, Legal, Public Accounting, Food and more. We are proactively building a data bank for opportunities in these fields. By applying, you ensure our recruiters can quickly match you with suitable roles when they arise.
Location: Various locations across Alberta As a Registered Nurse (RN) in the healthcare industry, you will provide high-quality patient care in various settings, including hospitals, clinics, and community health organizations. Your role is crucial in assessing patient needs, implementing care plans, and collaborating with healthcare teams to ensure optimal patient outcomes. Key Responsibilities: Conduct thorough assessments of patients' health status, including physical exams, medical histories, and vital sign monitoring.
Develop and implement individualized care plans based on patient assessments, ensuring they align with best practices and evidence-based guidelines. Safely administer medications and treatments as prescribed, monitoring patients for side effects and effectiveness. Educate patients and their families on health management, treatment plans, and preventive care strategies.
Work collaboratively with physicians, specialists, and other healthcare professionals to coordinate patient care and resolve health issues. Maintain accurate and timely documentation of patient care activities, assessments, and outcomes in electronic health records (EHR). Adhere to infection control protocols and safety standards to maintain a safe environment for patients and staff.
Act as a patient advocate, providing emotional support and guidance throughout the treatment process. Stay updated on current nursing practices, medical advancements, and regulatory changes through ongoing education and training. Requirements Bachelor's degree in Nursing (BSN) or an Associate's degree in Nursing (ADN) from an accredited program.
Valid state RN license and current CPR certification. Previous experience in a healthcare setting preferred, with specific experience in areas such as critical care, pediatrics, or geriatrics being advantageous. Strong clinical skills, critical thinking abilities, and excellent interpersonal communication skills.
Demonstrated ability to provide compassionate care and maintain patient confidentiality. Disclaimer: We're proactively building a databank for opportunities in Healthcare, Health Tech, Government, Non-Profits, Legal, and more. By applying, you ensure our recruiters can quickly match you with suitable roles when they arise.
We value Integrity, Transparency, and Innovation, so we want you to know these are not active jobs. Join our network today, and we'll promptly connect you with the right opportunities when they come up. Let us help you find your next career move.
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