Hamilton, ON · On-site
The Clinical Research Associate (CRA) assists the research team by performing delegated study tasks for academic and pharmaceutical sponsored clinical trials with significant responsibility for data ...
Hamilton, ON · On-site
The Clinical Research Associate (CRA) assists the research team by performing delegated study tasks for academic and pharmaceutical sponsored clinical trials with significant responsibility for data ...
Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Montreal Canada. We are an innovative, scientifically oriented mid-sized CRO that is ...
Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Montreal Canada. We are an innovative, scientifically oriented mid-sized CRO that is ...
Hamilton, ON · On-site
Clinical research experience preferred • Knowledge of medical terminology required • Analytical thinking and problem solving skills • Excellent written and verbal communication skills • ...
Hamilton, ON · On-site
Clinical research experience preferred • Knowledge of medical terminology required • Analytical thinking and problem solving skills • Excellent written and verbal communication skills • ...
... clinical research.
Position The Clinical Research Associate (CRA) will support the planning, start-up, execution, oversight, and closeout of assigned clinical studies. The CRA serves as an operational link among ...
Position The Clinical Research Associate (CRA) will support the planning, start-up, execution, oversight, and closeout of assigned clinical studies. The CRA serves as an operational link among ...
Mississauga, ON · On-site +1
CA$60K - CA$75K/yr
The Clinical Research Associate will be responsible for analyzing, questioning, and improving how work gets done while demonstrating strong foundational CRA capabilities, meeting business objectives ...
Mississauga, ON · On-site +1
CA$60K - CA$75K/yr
The Clinical Research Associate will be responsible for analyzing, questioning, and improving how work gets done while demonstrating strong foundational CRA capabilities, meeting business objectives ...
Mississauga, ON · On-site
CA$60K - CA$75K/yr
The Clinical Research Associate will be responsible for analyzing, questioning, and improving how work gets done while demonstrating strong foundational CRA capabilities, meeting business objectives ...
Quick apply
Mississauga, ON · On-site
CA$60K - CA$75K/yr
The Clinical Research Associate will be responsible for analyzing, questioning, and improving how work gets done while demonstrating strong foundational CRA capabilities, meeting business objectives ...
Acts as the main communication line between Monitor, Site Management Associate, Regional Project ... Advance your career in clinical research, coordinating a variety of tasks and learning new things ...
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Acts as the main communication line between Monitor, Site Management Associate, Regional Project ... Advance your career in clinical research, coordinating a variety of tasks and learning new things ...
CA$19.81 - CA$29.71/hr
As an Inventory Associate, you will be responsible for performing cycle counts, creating approvals ... With 550+ employees, including 100 dedicated sales and clinical professionals and eight ...
CA$19.81 - CA$29.71/hr
As an Inventory Associate, you will be responsible for performing cycle counts, creating approvals ... With 550+ employees, including 100 dedicated sales and clinical professionals and eight ...
Markham, ON · On-site
Train and mentor Clinical Trial Managers, Clinical Research Associates, and Clinical Trial Associates EDUCATION AND EXPERIENCE REQUIRED: * Bachelors Degree or 6 years relevant experience with a CRO ...
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Markham, ON · On-site
Train and mentor Clinical Trial Managers, Clinical Research Associates, and Clinical Trial Associates EDUCATION AND EXPERIENCE REQUIRED: * Bachelors Degree or 6 years relevant experience with a CRO ...
Train and mentor Clinical Trial Managers, Clinical Research Associates, and Clinical Trial Associates EDUCATION AND EXPERIENCE REQUIRED: * Bachelors Degree or 6 years relevant experience with a CRO ...
Train and mentor Clinical Trial Managers, Clinical Research Associates, and Clinical Trial Associates EDUCATION AND EXPERIENCE REQUIRED: * Bachelors Degree or 6 years relevant experience with a CRO ...
Hamilton, ON · On-site
Coordinate training of study teams/centers on all aspects of clinical study procedures. Coordinate ... This position may require evening and weekend shifts and is primarily located at the Offord Centre ...
Hamilton, ON · On-site
Coordinate training of study teams/centers on all aspects of clinical study procedures. Coordinate ... This position may require evening and weekend shifts and is primarily located at the Offord Centre ...
Hamilton, ON · On-site
Coordinate training of study teams/centers on all aspects of clinical study procedures. Coordinate ... This position may require evening and weekend shifts and is primarily located at the Offord Centre ...
Hamilton, ON · On-site
Coordinate training of study teams/centers on all aspects of clinical study procedures. Coordinate ... This position may require evening and weekend shifts and is primarily located at the Offord Centre ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH ...
... clinical research community with an emphasis on ethics, compliance, and innovation. Job Title ... Senior Quality Assurance Associate Location: Hybrid (Mississauga). 3 days per week in office, 2 ...
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... clinical research community with an emphasis on ethics, compliance, and innovation. Job Title ... Senior Quality Assurance Associate Location: Hybrid (Mississauga). 3 days per week in office, 2 ...
... clinical research community with an emphasis on ethics, compliance, and innovation. Job Title ... Senior Quality Assurance Associate Location: Hybrid (Mississauga). 3 days per week in office, 2 ...
... clinical research community with an emphasis on ethics, compliance, and innovation. Job Title ... Senior Quality Assurance Associate Location: Hybrid (Mississauga). 3 days per week in office, 2 ...
Mentor and coach Global Study Managers (GSMs) Clinical Research Associates (CRAs), and Global Study Associates (GSAs) to support professional development. * Lead Clinical Trial Working Groups (CTWGs)
New
Mentor and coach Global Study Managers (GSMs) Clinical Research Associates (CRAs), and Global Study Associates (GSAs) to support professional development. * Lead Clinical Trial Working Groups (CTWGs)
New
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Toronto, ON · On-site
CA$400K/yr
... Associate/ Full Professor commensurate with their qualification and academic achievement. The ... Sunnybrook has an international reputation for clinical and research excellence and is an ...
Toronto, ON · On-site
CA$400K/yr
... Associate/ Full Professor commensurate with their qualification and academic achievement. The ... Sunnybrook has an international reputation for clinical and research excellence and is an ...
Toronto, ON · Remote
... clinical research standards. Responsibilities : * Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files ...
Toronto, ON · Remote
... clinical research standards. Responsibilities : * Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files ...
The most popular types of Weekend Clinical Research jobs in Toronto, ON are:
Full-time
Re-posted 17 days ago
The Clinical Research Associate (CRA) assists the research team by performing delegated study tasks for academic and pharmaceutical sponsored clinical trials with significant responsibility for data management. The CRA is responsible for extracting patient information from the electronic health record (EHR) and accurately and efficiently entering data into the sponsor provided electronic data capture (EDC) system. The CRA asks questions to clarify issues related to data integrity, and applies knowledge of internal policies and procedures and national research regulations and guidelines to ensure research activities are carried out in a compliant manner. The CRA communicates patient-specific and/or protocol compliance issues to the Research Coordinator and Investigator, as applicable. The CRA may coordinate and manage minimal risk, non-invasive and/or non-interventional clinical trials from activation to close out, adhering to the study protocol and requlatory requirements including entering study required patient assessment findings in the EHR within scope of practice. Performs other administrative duties as required.
• Bachelor’s degree in a health or science-related discipline required
• Clinical Research Graduate Certificate preferred
• Certification as a Clinical Research Professional (SoCRA or ACRP) an asset
• 1-2 years previous related experience; Clinical research experience preferred
• Knowledge of medical terminology required
• Analytical thinking and problem solving skills
• Excellent written and verbal communication skills
• Knowledge of ICH-GCP guidelines, Health Canada Food and Drug Regulations, and Tri-Council Policy Statement 2 (TCPS-2)
• Basic knowledge of clinical research principles, practices, and processes related to project management, study coordination, regulatory requirements, data collection and reporting
• Highly proficient computer skills
• Experience using electronic health records and data management software applications preferred
• Ability to organize workload to meet deadlines and flexible when priorities change
• Ability to push/pull carts with patient charts/case reports
• Follows health and safety policies and procedures to ensure a safe workplace for self and others
