Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Clinical Research Associate
Montreal, QC · On-site
Reporting to a CRA Line Manager , this position will be home-based in Canada. Responsibilities ... Performing data verification of source documents; * Ensuring implementation and compliance with FDA ...
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Clinical Research Associate
Montreal, QC · On-site
Reporting to a CRA Line Manager , this position will be home-based in Canada. Responsibilities ... Performing data verification of source documents; * Ensuring implementation and compliance with FDA ...
Clinical Research Coordinator
Montreal, QC · Hybrid
CA$33.05 - CA$40.97/hr
Serve as liaison between researchers, participants, the Clinical Research Manager and the Program Manager. Data, Sample & Regulatory Oversight * Maintain study documentation (e.g., Investigator Site ...
Clinical Research Coordinator
Montreal, QC · Hybrid
CA$33.05 - CA$40.97/hr
Serve as liaison between researchers, participants, the Clinical Research Manager and the Program Manager. Data, Sample & Regulatory Oversight * Maintain study documentation (e.g., Investigator Site ...
Clinical Research Coordinator
Montreal, QC · Hybrid
CA$33.05 - CA$40.97/hr
Serve as liaison between researchers, participants, the Clinical Research Manager and the Program Manager. Data, Sample & Regulatory Oversight * Maintain study documentation (e.g., Investigator Site ...
Clinical Research Coordinator
Montreal, QC · Hybrid
CA$33.05 - CA$40.97/hr
Serve as liaison between researchers, participants, the Clinical Research Manager and the Program Manager. Data, Sample & Regulatory Oversight * Maintain study documentation (e.g., Investigator Site ...
Clinical Research Nurse
Beaumont, QC · On-site
About The Role The Clinical Research Nurse will oversee the safety and consent of clinical trial ... Other tasks as assigned by management. What You'll Need to Succeed * DEC from accredited Registered ...
Clinical Research Nurse
Beaumont, QC · On-site
About The Role The Clinical Research Nurse will oversee the safety and consent of clinical trial ... Other tasks as assigned by management. What You'll Need to Succeed * DEC from accredited Registered ...
Clinical Research Technician
Beaumont, QC · On-site
About the role The Clinical Research Technician will work with Clinic teams to execute clinical ... Other tasks as assigned by management. What you'll need to succeed * High School Diploma or/and ...
Clinical Research Technician
Beaumont, QC · On-site
About the role The Clinical Research Technician will work with Clinic teams to execute clinical ... Other tasks as assigned by management. What you'll need to succeed * High School Diploma or/and ...
Under the direction of the Scientific Manager, the Assistant Manager will support the Clinical Research Unit and The Neuro in its mission to deliver cutting-edge and specialized clinical trials. The ...
Under the direction of the Scientific Manager, the Assistant Manager will support the Clinical Research Unit and The Neuro in its mission to deliver cutting-edge and specialized clinical trials. The ...
Under the direction of the Scientific Manager, the Assistant Manager will support the Clinical Research Unit and The Neuro in its mission to deliver cutting-edge and specialized clinical trials. The ...
Under the direction of the Scientific Manager, the Assistant Manager will support the Clinical Research Unit and The Neuro in its mission to deliver cutting-edge and specialized clinical trials. The ...
... data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
... data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
We're looking for a Senior Clinical Research Associate to serve as the primary link between ... Partnering across data management, project management, and medical teams to influence enrollment ...
We're looking for a Senior Clinical Research Associate to serve as the primary link between ... Partnering across data management, project management, and medical teams to influence enrollment ...
Work with R&D, Product Management, and Operations to support the creation of new items across ... Ensure lifecycle data supports sustaining activities such as redesign, obsolescence management, and ...
Work with R&D, Product Management, and Operations to support the creation of new items across ... Ensure lifecycle data supports sustaining activities such as redesign, obsolescence management, and ...
IQVIA is seeking experienced Clinical Data Team Leads to oversee end-to-end data management ... Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ...
IQVIA is seeking experienced Clinical Data Team Leads to oversee end-to-end data management ... Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ...
Product Data Manager
Brossard, QC · On-site
Work with R&D, Product Management, and Operations to support the creation of new items across ... Ensure lifecycle data supports sustaining activities such as redesign, obsolescence management, and ...
Product Data Manager
Brossard, QC · On-site
Work with R&D, Product Management, and Operations to support the creation of new items across ... Ensure lifecycle data supports sustaining activities such as redesign, obsolescence management, and ...
... on Fortrea or client data management systems, as assigned by management. * Assistwith the ... research, data analysis, datamanagementor technical writing). * 1-2 years of clinical research ...
... on Fortrea or client data management systems, as assigned by management. * Assistwith the ... research, data analysis, datamanagementor technical writing). * 1-2 years of clinical research ...
Performing data review and resolution of queries to maintain high-quality clinical data ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Performing data review and resolution of queries to maintain high-quality clinical data ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
In this role, you will collaborate with cross-functional teams, including clinical research associates (CRAs), data managers, and regulatory personnel, to deliver high-quality clinical data while ...
In this role, you will collaborate with cross-functional teams, including clinical research associates (CRAs), data managers, and regulatory personnel, to deliver high-quality clinical data while ...
Clinical Trial Manager
Montreal, QC · On-site
Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout ... Manages country deliverables, timelines and results for assigned protocols to meet country ...
Clinical Trial Manager
Montreal, QC · On-site
Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout ... Manages country deliverables, timelines and results for assigned protocols to meet country ...
Clinical Trial Manager
Montreal, QC · On-site
Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout ... Manages country deliverables, timelines and results for assigned protocols to meet country ...
Clinical Trial Manager
Montreal, QC · On-site
Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout ... Manages country deliverables, timelines and results for assigned protocols to meet country ...
Clinical Research Data Manager information
See Quebec salary details
$11.30 - $16.35
6% of jobs
$16.35 - $21.39
16% of jobs
$22.14 is the 25th percentile. Wages below this are outliers.
$21.39 - $26.44
18% of jobs
$26.44 - $31.49
7% of jobs
The median wage is $33.51 / hr.
$31.49 - $36.54
5% of jobs
$36.54 - $41.59
3% of jobs
$41.59 - $46.63
11% of jobs
$50.84 is the 75th percentile. Wages above this are outliers.
$46.63 - $51.68
10% of jobs
$51.68 - $56.73
11% of jobs
$56.73 - $61.78
6% of jobs
$61.78 - $66.83
6% of jobs
$11
$38
$66
How much do clinical research data manager jobs pay per hour?
What is a clinical research data manager?
What are some common challenges faced by clinical research data managers during multi-site trials?
What are the key skills and qualifications needed to thrive as a clinical research data manager, and why are they important?
What is the difference between Clinical Research Data Manager vs Clinical Research Coordinator?
| Aspect | Clinical Research Data Manager | Clinical Research Coordinator |
|---|---|---|
| Primary Role | Oversees data collection, management, and quality control of clinical trial data. | Coordinates daily trial activities, patient recruitment, and site management. |
| Required Skills | Data management, database systems, regulatory compliance. | Patient interaction, study protocol adherence, site coordination. |
| Work Environment | Data centers, clinical trial sites, research organizations. | Clinical sites, hospitals, research facilities. |
| Common Certifications | CDMP, SAS, or related data management certifications. | GCP certification, clinical trial training. |
While both roles support clinical research, the Clinical Research Data Manager focuses on data integrity and management, whereas the Clinical Research Coordinator handles trial operations and participant coordination. Understanding these differences helps in choosing the right career path or job search focus.
What job categories do people searching Clinical Research Data Manager jobs in Quebec look for?
The top searched job categories for Clinical Research Data Manager jobs in Quebec are:
What cities in Quebec are hiring for Clinical Research Data Manager jobs?
Cities in Quebec with the most Clinical Research Data Manager job openings:

Full-time
Medical, Retirement, PTO
Re-posted 7 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
16th of 75 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