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 ...
Sr CRA
Montreal, QC · On-site
As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. This is a sponsor dedicated ...
Sr CRA
Montreal, QC · On-site
As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. This is a sponsor dedicated ...
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 ...
Senior CRA
Montreal, QC · On-site
Senior CRA 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 organisation ...
Senior CRA
Montreal, QC · On-site
Senior CRA 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 organisation ...
The Senior CRA II is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory ...
The Senior CRA II is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory ...
As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. This is a sponsor dedicated ...
As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. This is a sponsor dedicated ...
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
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, IQVIA Biotech
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
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 ...
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 ...
Bilingual Tax Administrator
Montreal, QC · On-site
The Tax Administrator processes all tax monthly withholding tax remittances and delivered within SLA, CRA, MRQ and IRS filing deadlines. The Tax Administrator will ensure that all trustee and ...
Bilingual Tax Administrator
Montreal, QC · On-site
The Tax Administrator processes all tax monthly withholding tax remittances and delivered within SLA, CRA, MRQ and IRS filing deadlines. The Tax Administrator will ensure that all trustee and ...
The CRA will liaise with Quality Assurance (QA), Medical Information Team, Marketing or Sales Teams. The CRA receives temperature excursion assessment requests from customers or 3PL (direct shipments ...
Quick apply
Apply Early
The CRA will liaise with Quality Assurance (QA), Medical Information Team, Marketing or Sales Teams. The CRA receives temperature excursion assessment requests from customers or 3PL (direct shipments ...
Apply Early
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 ...
Our FSP team is currently seeking a French Speaking Sr. CRA 2 with 4+ years of monitoring as well as strong Oncology monitoring experience residing in Montreal, Canada. WHAT YOU WILL DO You will ...
Our FSP team is currently seeking a French Speaking Sr. CRA 2 with 4+ years of monitoring as well as strong Oncology monitoring experience residing in Montreal, Canada. WHAT YOU WILL DO You will ...
Senior Clinical Research Associate
Montreal, QC · On-site +1
Senior CRA / CRA II - Home-Based (CAN) 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 ...
Senior Clinical Research Associate
Montreal, QC · On-site +1
Senior CRA / CRA II - Home-Based (CAN) 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 ...
In the function of Lead CRA, will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans, protocols, CRFs, communications or other ...
In the function of Lead CRA, will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans, protocols, CRFs, communications or other ...
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?
What are Clinical Research Associates (CRAs)?
How does a CRA (Clinical Research Associate) 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.

Other
Medical, Retirement, PTO
Posted 6 days ago
Medpace rating
8.5
Based on 9 frontline employees who took The Breakroom Quiz
12th of 58 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 1 year 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). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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