Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched by other CROs! Responsibilities * Conduct pre-study, initiation, monitoring, and closeout visits for ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched by other CROs! Responsibilities * Conduct pre-study, initiation, monitoring, and closeout visits for ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched by other CROs! Responsibilities * Conduct pre-study, initiation, monitoring, and closeout visits for ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched by other CROs! Responsibilities * Conduct pre-study, initiation, monitoring, and closeout visits for ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched by other CROs! Responsibilities * Conduct pre-study, initiation, monitoring, and closeout visits for ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched by other CROs! Responsibilities * Conduct pre-study, initiation, monitoring, and closeout visits for ...
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)
Montreal, QC · On-site
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to ...
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)
Montreal, QC · On-site
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to ...
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Mo...
Montreal, QC · On-site
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Montreal, Quebec, Canada) Syneos Health is a leading fully integrated biopharmaceutical solutions ...
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Mo...
Montreal, QC · On-site
CRA II / Sr CRA - Sponsor Dedicated | Oncology | Bilingual in French and English (Home-Based - Montreal, Quebec, Canada) Syneos Health is a leading fully integrated biopharmaceutical solutions ...
Study Start Up CRA
Montreal, QC · On-site
The Study Start Up CRA is accountable for site selections as well as study specific start up activities and deliverables of assigned sites for Phase I-IV trials in the country in accordance with ...
Study Start Up CRA
Montreal, QC · On-site
The Study Start Up CRA is accountable for site selections as well as study specific start up activities and deliverables of assigned sites for Phase I-IV trials in the country in accordance with ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Kirkland, QC · On-site
Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Kirkland, QC · On-site
Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology
Kirkland, QC · On-site
Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology
Kirkland, QC · On-site
Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Quebec, QC · On-site
Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Quebec, QC · On-site
Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Laval, QC · On-site
Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Laval, QC · On-site
Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. You will manage site activities from ...
CRA II - phase I ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
CRA II - phase I ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
Some organizations require completion of CRA training program or prior monitoring experience. Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e ...
Some organizations require completion of CRA training program or prior monitoring experience. Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e ...
Vice President, Registered Plans & Estate Settlements
CA$130K - CA$140K/yr
Adhere to all CRA & Trustee reporting obligations; * Work with our vendor relationships to implement enhancements or regulated changes to our Registered Plan recordkeeping and processing software;
Vice President, Registered Plans & Estate Settlements
CA$130K - CA$140K/yr
Adhere to all CRA & Trustee reporting obligations; * Work with our vendor relationships to implement enhancements or regulated changes to our Registered Plan recordkeeping and processing software;
Senior Adviser, Payroll Tax & Accounting | Conseiller(ere) senior, Fiscalite de la paie et compta...
Montreal, QC · Hybrid
Provide oversight for CRA and MRQ compliance, DAS remittances and reconciliations, CPP, EI, and provincial tax obligations. * Drive the end-to-end delivery of year-end tax reporting, including T4 ...
Senior Adviser, Payroll Tax & Accounting | Conseiller(ere) senior, Fiscalite de la paie et compta...
Montreal, QC · Hybrid
Provide oversight for CRA and MRQ compliance, DAS remittances and reconciliations, CPP, EI, and provincial tax obligations. * Drive the end-to-end delivery of year-end tax reporting, including T4 ...
Coordonner et gerer les activites des Associe de recherche Clinique (CRA) dans toutes les zones geographiques, en assurant la liaison avec le promoteur, le chef de projet et les autres responsables ...
Coordonner et gerer les activites des Associe de recherche Clinique (CRA) dans toutes les zones geographiques, en assurant la liaison avec le promoteur, le chef de projet et les autres responsables ...
Faconner la prochaine generation d'ARC (CRA) grace a un mentorat pratique, a des visites accompagnees et a un partage des connaissances qui eleve le niveau de l'ensemble de l'equipe * Collaborer avec ...
New
Faconner la prochaine generation d'ARC (CRA) grace a un mentorat pratique, a des visites accompagnees et a un partage des connaissances qui eleve le niveau de l'ensemble de l'equipe * Collaborer avec ...
New
Senior CRA / CRA II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
Senior CRA / CRA II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
CRA, ISO/SAE 21434, RED-DA, IEC 62443, NIST, etc. Qualifications * Bachelor's or Master's degree in Software, Electrical, Computer, or Automotive Engineering or a related field. * 3-10 years of ...
Quick apply
CRA, ISO/SAE 21434, RED-DA, IEC 62443, NIST, etc. Qualifications * Bachelor's or Master's degree in Software, Electrical, Computer, or Automotive Engineering or a related field. * 3-10 years of ...
Strong knowledge of ISO/SAE 21434 and UNECE R155/R156 requirements, with familiarity with the EU Cyber Resilience Act (CRA) and related cybersecurity regulatory frameworks. * Ability to objectively ...
Strong knowledge of ISO/SAE 21434 and UNECE R155/R156 requirements, with familiarity with the EU Cyber Resilience Act (CRA) and related cybersecurity regulatory frameworks. * Ability to objectively ...
Ingénieur électrique
Quebec, QC · On-site
... CRA,
Ingénieur électrique
Quebec, QC · On-site
... CRA,
Cra information
See Quebec salary details
$13.70 - $21.15
4% of jobs
$21.15 - $28.61
14% of jobs
$31.56 is the 25th percentile. Wages below this are outliers.
$28.61 - $36.06
18% of jobs
$36.06 - $43.51
13% of jobs
The median wage is $44.25 / hr.
$43.51 - $50.96
16% of jobs
$55.45 is the 75th percentile. Wages above this are outliers.
$50.96 - $58.41
18% of jobs
$58.41 - $65.87
9% of jobs
$65.87 - $73.32
4% of jobs
$73.32 - $80.77
3% of jobs
$80.77 - $88.22
0% of jobs
$88.22 - $95.67
1% of jobs
$13
$47
$95
How much do cra jobs pay per hour?
What is a CRA?
A CRA, or clinical research associate, is an investigator who makes sure that medical research follows protocols and meets ethical standards. The primary responsibilities of CRAs include monitoring clinical research trials to verify the accuracy of the trial data as well as the safety and well-being of patients. To carry out these duties, CRAs visit the clinical sites where a study takes place, such as hospitals and other facilities, review documents, and observe trial proceedings.
What are the key skills and qualifications needed to thrive as a Chartered Accountant (CA), and why are they important?
How does a CRA typically collaborate with site staff and sponsors during a clinical trial?
What is the difference between Cra vs Clinical Research Associate?
| Aspect | Cra | Clinical Research Associate |
|---|---|---|
| Credentials | Typically requires a degree in life sciences or related field; certifications like CCRP or RAC are common | Same as Cra, often holds certifications like CCRP or RAC |
| Work Environment | Works on clinical trial sites or in offices, monitoring study progress | Monitors clinical trials, manages site compliance, and ensures protocol adherence |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Pharmaceutical companies, CROs, biotech firms |
The term Cra is often used interchangeably with Clinical Research Associate, as both roles involve monitoring clinical trials, ensuring compliance, and working within the same industry. The main difference is that Cra is a broader abbreviation, while Clinical Research Associate is the full job title. Both require similar credentials and work environments, making them essentially the same role described differently.
Is it hard to get a CRA job?
What is the job of a clinical research associate?
What are popular job titles related to Cra jobs in Quebec?
For Cra jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Cra jobs in Quebec look for?
The top searched job categories for Cra jobs in Quebec are:
What cities in Quebec are hiring for Cra jobs?
Cities in Quebec with the most Cra job openings:
What are popular job titles related to Cra jobs in QC?
For Cra jobs in QC, the most frequently searched job titles are:

Full-time
Medical, Retirement, PTO
Re-posted 23 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 Montreal 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
-
- 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
-
- 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