Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science from an accredited university; * At least 2 years as a Clinical Research Associate or Clinical ...
Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science from an accredited university; * At least 2 years as a Clinical Research Associate or Clinical ...
The Opportunity Tiny Health is seeking a Director of Clinical Research to co-own the strategy ... Oversee protocol development, statistical analysis plans, and data collection frameworks * Manage ...
Quick apply
The Opportunity Tiny Health is seeking a Director of Clinical Research to co-own the strategy ... Oversee protocol development, statistical analysis plans, and data collection frameworks * Manage ...
Study Coordinator - Clinical Research
$50K - $55K/yr
... early phase clinical trails in healthy volunteers, special and patient populations. We are ... generate data in compliance with protocols, Pharma Medica Research Inc.'s (PMRI's) SOPs, GCP ...
Study Coordinator - Clinical Research
$50K - $55K/yr
... early phase clinical trails in healthy volunteers, special and patient populations. We are ... generate data in compliance with protocols, Pharma Medica Research Inc.'s (PMRI's) SOPs, GCP ...
Study Coordinator - Clinical Research
Toronto, ON · On-site
CA$50K - CA$55K/yr
... early phase clinical trails in healthy volunteers, special and patient populations. We are ... generate data in compliance with protocols, Pharma Medica Research Inc.'s (PMRI's) SOPs, GCP ...
Quick apply
Study Coordinator - Clinical Research
Toronto, ON · On-site
CA$50K - CA$55K/yr
... early phase clinical trails in healthy volunteers, special and patient populations. We are ... generate data in compliance with protocols, Pharma Medica Research Inc.'s (PMRI's) SOPs, GCP ...
The CRA asks questions to clarify issues related to data integrity, and applies knowledge of ... Clinical research experience preferred • Knowledge of medical terminology required • Analytical ...
The CRA asks questions to clarify issues related to data integrity, and applies knowledge of ... Clinical research experience preferred • Knowledge of medical terminology required • Analytical ...
Clinical Research Study Assistant Employment Status: Temporary Part Time Duration: December 31 2026 ... Data Collection & Management: * May assist with the collection of medical documents as per approved ...
Clinical Research Study Assistant Employment Status: Temporary Part Time Duration: December 31 2026 ... Data Collection & Management: * May assist with the collection of medical documents as per approved ...
Clinical Research Study Assistant Employment Status: Temporary Part Time Duration: December 31 2026 ... Data Collection & Management: * May assist with the collection of medical documents as per approved ...
Clinical Research Study Assistant Employment Status: Temporary Part Time Duration: December 31 2026 ... Data Collection & Management: * May assist with the collection of medical documents as per approved ...
Data Management Assistant
Hamilton, ON · On-site
The Data Management Assistant's overall purpose is the verification of study data while developing ... Conduct conference calls with the Sponsor and Clinical Research Associates for site updates.
Data Management Assistant
Hamilton, ON · On-site
The Data Management Assistant's overall purpose is the verification of study data while developing ... Conduct conference calls with the Sponsor and Clinical Research Associates for site updates.
Clinical research experience preferred • Knowledge of medical terminology required • Analytical ... data collection and reporting • Highly proficient computer skills • Experience using electronic ...
Clinical research experience preferred • Knowledge of medical terminology required • Analytical ... data collection and reporting • Highly proficient computer skills • Experience using electronic ...
Role Summary At Wisedocs, Medical Data Annotators pair clinical expertise with technology to transform how records are handled - helping insurers, legal teams, and healthcare organizations cut ...
Role Summary At Wisedocs, Medical Data Annotators pair clinical expertise with technology to transform how records are handled - helping insurers, legal teams, and healthcare organizations cut ...
Role Summary At Wisedocs, Medical Data Annotators pair clinical expertise with technology to transform how records are handled -- helping insurers, legal teams, and healthcare organizations cut ...
Quick apply
Role Summary At Wisedocs, Medical Data Annotators pair clinical expertise with technology to transform how records are handled -- helping insurers, legal teams, and healthcare organizations cut ...
Position The Clinical Research Associate (CRA) will support the planning, start-up, execution ... The role helps ensure participant protection, reliable study data, timely site execution, and ...
New
Position The Clinical Research Associate (CRA) will support the planning, start-up, execution ... The role helps ensure participant protection, reliable study data, timely site execution, and ...
New
Clinical Research Associate
Mississauga, ON · On-site +1
CA$60K - CA$75K/yr
General Accountability: The Clinical Research Associate will be responsible for analyzing ... Ensure study data are accurate, complete, and verifiable through source data review/verification ...
Clinical Research Associate
Mississauga, ON · On-site +1
CA$60K - CA$75K/yr
General Accountability: The Clinical Research Associate will be responsible for analyzing ... Ensure study data are accurate, complete, and verifiable through source data review/verification ...
Clinical Research Associate
Mississauga, ON · On-site
CA$60K - CA$75K/yr
General Accountability: The Clinical Research Associate will be responsible for analyzing ... Ensure study data are accurate, complete, and verifiable through source data review/verification ...
Quick apply
Clinical Research Associate
Mississauga, ON · On-site
CA$60K - CA$75K/yr
General Accountability: The Clinical Research Associate will be responsible for analyzing ... Ensure study data are accurate, complete, and verifiable through source data review/verification ...
Research Associate
Toronto, ON · On-site
CA$49.91 - CA$62.43/hr
Strong data management, analytical and scientific writing skills * Expertise in qualitative research methodologies, clinical trials, and / or observational studies using administrative data
Research Associate
Toronto, ON · On-site
CA$49.91 - CA$62.43/hr
Strong data management, analytical and scientific writing skills * Expertise in qualitative research methodologies, clinical trials, and / or observational studies using administrative data
Research Coordinator
Richmond Hill, ON · On-site +1
The Research Coordinator plays a central role in supporting and overseeing all research activities ... Experience with clinical data collection from electronic medical charts. * Demonstrated proficiency ...
Research Coordinator
Richmond Hill, ON · On-site +1
The Research Coordinator plays a central role in supporting and overseeing all research activities ... Experience with clinical data collection from electronic medical charts. * Demonstrated proficiency ...
Research Coordinator
Maple, ON · On-site +1
The Research Coordinator plays a central role in supporting and overseeing all research activities ... Experience with clinical data collection from electronic medical charts. * Demonstrated proficiency ...
Research Coordinator
Maple, ON · On-site +1
The Research Coordinator plays a central role in supporting and overseeing all research activities ... Experience with clinical data collection from electronic medical charts. * Demonstrated proficiency ...
Ensures ongoing evaluation of data integrity and compliance at a country/regional level. * Conducts ... Advance your career in clinical research, coordinating a variety of tasks and learning new things ...
Ensures ongoing evaluation of data integrity and compliance at a country/regional level. * Conducts ... Advance your career in clinical research, coordinating a variety of tasks and learning new things ...
Clinical Data Analyst
Toronto, ON · Remote
Preference to prior Clinical Research and/or Clinical Data Management experience. Working Condition * Home-based $89,000 - $148,000 a year + bonus We may use artificial intelligence (AI) tools to ...
Clinical Data Analyst
Toronto, ON · Remote
Preference to prior Clinical Research and/or Clinical Data Management experience. Working Condition * Home-based $89,000 - $148,000 a year + bonus We may use artificial intelligence (AI) tools to ...
Clinical Coordinator
Toronto, ON · Remote
... related research * Familiarity with electronic data capture tools, clinical trial management ... systems, or REDCap * Experience coordinating external partners, sites, or CROs * Work experience in ...
Quick apply
Clinical Coordinator
Toronto, ON · Remote
... related research * Familiarity with electronic data capture tools, clinical trial management ... systems, or REDCap * Experience coordinating external partners, sites, or CROs * Work experience in ...
Clinical Research Data Abstractor information
What is a clinical research data abstractor?
What skills and qualifications are needed to be a clinical research data abstractor?
What are common challenges faced by clinical research data abstractors, and how can they be managed?
What is the difference between Clinical Research Data Abstractor vs Clinical Research Coordinator?
| Aspect | Clinical Research Data Abstractor | Clinical Research Coordinator |
|---|---|---|
| Primary Role | Extracts and summarizes data from clinical trial records | Manages overall study operations and participant coordination |
| Required Skills | Attention to detail, data management, basic medical knowledge | Regulatory compliance, patient interaction, study oversight |
| Work Environment | Data entry labs, clinical trial sites, research offices | Clinical sites, hospitals, research institutions |
| Certifications | Typically none required, but certifications like CCR can help | Often requires CCRC or similar certifications |
While both roles support clinical research, the Clinical Research Data Abstractor focuses on data extraction and analysis, whereas the Clinical Research Coordinator manages study logistics and participant interactions. Understanding these differences helps in choosing the right career path or job search focus.
What are popular job titles related to Clinical Research Data Abstractor jobs in Toronto, ON?
For Clinical Research Data Abstractor jobs in Toronto, ON, the most frequently searched job titles are:
What job categories do people searching Clinical Research Data Abstractor jobs in Toronto, ON look for?
The top searched job categories for Clinical Research Data Abstractor jobs in Toronto, ON are:
- Clinical Research Organization
- Clinical Research Assistant
- Entry Level Biotech Clinical Research
- Manager Visa Sponsorship Clinical Research
- Clinical Research Associate
- Remote Clinical Research Dental
- Research Coordinator
- Clinical Research Associate Sponsor Dedicated
- Clinical Research Program Manager
- Clinical Research Project Manager

Full-time
Medical, Retirement, PTO
Re-posted 29 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
14th of 74 rated research
Job description
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 focused on full-service project work.
This is a home-based position in Canada.
Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems.
WE OFFER THE FOLLOWING
- Competitive bonus plans including Resourcing Bonus (following training completion and successful assignment to studies) and Yearly Travel Incentives
- Voluntary retirement scheme
- Home office furniture allowance, mobile phone and hotspot for internet access anywhere
- In-house travel agents, reimbursement for airline club and TSA pre-check
- Customized PACE training program based on your experience and therapeutic background and interest
- User friendly CTMS with electronic submission and approval of monitoring visit reports
- Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
- National assignments with average of 2 protocols
- In-house administrative support for all levels of CRAs
- Opportunities to work with international team of CRAs
- Low turnover rates for CRAs
- No metric for minimum required days on site per month
- Flexible work hours across days within a week
- Opportunity for CRA leadership positions - Lead CRA, CRA Manager
- Many additional perks unmatched by other CROs!
- Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;
- Maintain ongoing site correspondence and site files;
- Complete visit reports and maintaining study-related databases;
- Oversight and interaction with clinical research sites; and
- Review of patient charts and clinical research data.
- Bachelor's degree in science from an accredited university;
- At least 2 years as a Clinical Research Associate or Clinical Research Coordinator;
- Bilingual in English and French;
- Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ICH E-6 guidelines and per Part-C, Division 5 of the Health Canada Food and Drug regulations;
- Excellent interpersonal, written and verbal communication skills in English and French;
- Strong attention to detail and organization skills;
- Highly motivated, independent, flexible;
- Ability to travel between 60-80%;
- Ability to prioritize workload to meet timelines across multiple studies; and
- Proficient in Microsoft Office.
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
-
- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
-
- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
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- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
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- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Employment Type: OTHERAbout Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992