Reviews and interprets significant clinical laboratory reports on a daily basis for the purpose of ... visitors, associates and community partners * acting as a resource/consultant for infection ...
Reviews and interprets significant clinical laboratory reports on a daily basis for the purpose of ... visitors, associates and community partners * acting as a resource/consultant for infection ...
Collaborate across multiple functions, including research, clinical, and manufacturing teams-to ... May design, conduct, and interpret complex pharmacokinetics, drug metabolism, and ADME studies ...
New
Collaborate across multiple functions, including research, clinical, and manufacturing teams-to ... May design, conduct, and interpret complex pharmacokinetics, drug metabolism, and ADME studies ...
New
Clinical Study Associate information
See Kitchener, ON salary details
$18.39 - $22.20
23% of jobs
$23.35 is the 25th percentile. Wages below this are outliers.
$22.20 - $26.02
5% of jobs
$26.02 - $29.83
12% of jobs
$29.83 - $33.64
4% of jobs
The median wage is $34.76 / hr.
$33.64 - $37.45
18% of jobs
$37.45 - $41.27
7% of jobs
$44.13 is the 75th percentile. Wages above this are outliers.
$41.27 - $45.08
6% of jobs
$45.08 - $48.89
10% of jobs
$48.89 - $52.70
5% of jobs
$52.70 - $56.52
4% of jobs
$56.52 - $60.33
4% of jobs
$18
$36
$60
How much do clinical study associate jobs pay per hour?
As of Sep 3, 2026, the average hourly pay for clinical study associate in Kitchener, ON is $36.63, according to ZipRecruiter salary data. Most workers in this role earn between $26.02 and $46.87 per hour, depending on experience, location, and employer.
What is a clinical study associate?
Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.
What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?
Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
What are the key skills and qualifications needed to thrive as a clinical study associate, and why are they important?
To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.
What is the difference between Clinical Study Associate vs Clinical Research Coordinator?
| Aspect | Clinical Study Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficial | Bachelor's degree in health sciences or related field; certifications like CCRP advantageous |
| Work Environment | Pharmaceutical companies, CROs, clinical trial sites | Hospitals, clinics, research centers |
| Job Focus | Monitoring clinical trials, ensuring protocol compliance, data accuracy | Managing daily trial activities, patient recruitment, data collection |
| Employer & Industry Usage | Commonly employed in pharma and CROs | Primarily in healthcare and academic research settings |
Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.
What cities near Kitchener, ON are hiring for Clinical Study Associate jobs?
Cities near Kitchener, ON with the most Clinical Study Associate job openings:
Part-time
Re-posted 22 days ago
Job description
Supports the Infection Prevention and Control Program for Hamilton Health Sciences at all sites:
Follows national guidelines /best practices for the surveillance of healthcare associated infections
Follows the Public Health Act (HPPA) for the reporting of communicable infectious diseases
Reviews patient records to ascertain clinical signs and symptoms for infection, clinical interventions and requirements for transmission-based precautions. Completes patient specific information.
Reviews and interprets significant clinical laboratory reports on a daily basis for the purpose of ongoing surveillance/trends
Interviews hospital patients or out-patients as necessary to complete the patient-specific data
Gathers and calculates infection control statistics such as averages, percentages and rates in support of the infection prevention and control program.
Investigates all infection clusters and outbreaks with interventions directed at infection prevention
Consults for infection risk assessment, prevention and control strategies to departments
Participates or consults in the development and maintenance of Infection Prevention and Control protocols/ standards/policy and procedures
Provides after hours and weekend on-call services as required and occasional week ends on site coverage
Assists in research projects with bibliographic searches, statistical computations, drafting of reports/ papers and publications
Supports Program activities as requested by the Infection Control /Manager, which may include:
* responding to inquiries from hospital staff, patient, visitors, associates and community partners
* acting as a resource/consultant for infection prevention and control issues
participating in the preparation and implementation of educational programs that the support the goals of the department
* implements changes mandated by regulatory and licensing agencies consulting on product evaluation and recommendations for infection prevention and control implications
* Attends and participates in hospital-related committees as directed by the Infection Control Officer/Manager
Bachelor's degree in Nursing or other Regulated Healthcare Professional discipline or University degree in a heath
sciences field
Successful completion of an IPAC-Canada endorsed basic training course in Infection Prevention and Control
Two years experience working in an Infection Prevention and Control Program
Certificate in Infection Control (CIC designation) by the Certification Board of Infection Control
Regulated Health Care Professional with current registration with their professional body
Knowledge of acute, and ambulatory care programs an asset
Demonstrated knowledge and experience in the complexities of the delivery of patient care
Ability to communicate successfully with staff, families and community partners
Computer proficiencies: MS Word, MS Excel and PowerPoint, familiarity with statistical software preferred
Demonstrated experience in adult education techniques
Effective research skills including ability to construct effective studies involving statistical measures an asset
Self-motivated , flexible and able to work effectively with minimal supervision
Consistent and regular attendance required