The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good ... Monitor, document and/or follow-up on participant adverse events. * Maintain and advocate a high ...
The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good ... Monitor, document and/or follow-up on participant adverse events. * Maintain and advocate a high ...
Senior Clinical Research Associate
Montreal, QC · On-site +1
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported ...
Senior Clinical Research Associate
Montreal, QC · On-site +1
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported ...
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported ...
As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported ...
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: * Conducting site qualification ...
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: * Conducting site qualification ...
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to ... Review of patient charts and clinical research data. Qualifications * Bachelor's degree in science ...
Site Monitoring activities (55-60%) * Independently conduct and document onsite and remote ... Coordinate the shipment of clinical supplies, including but not limited to, investigational product ...
Site Monitoring activities (55-60%) * Independently conduct and document onsite and remote ... Coordinate the shipment of clinical supplies, including but not limited to, investigational product ...
Site Monitoring activities (55-60%) * Independently conduct and document onsite and remote ... Coordinate the shipment of clinical supplies, including but not limited to, investigational product ...
Site Monitoring activities (55-60%) * Independently conduct and document onsite and remote ... Coordinate the shipment of clinical supplies, including but not limited to, investigational product ...
Research Assistant 1
Montreal, QC · On-site
CA$30.54/hr
... monitor questionnaire completion (e.g. REDCap), and coordinate biospecimen collection. (v) Work jointly with the Clinical Research Unit (CRU) to identify and refer eligible patients for clinical ...
Research Assistant 1
Montreal, QC · On-site
CA$30.54/hr
... monitor questionnaire completion (e.g. REDCap), and coordinate biospecimen collection. (v) Work jointly with the Clinical Research Unit (CRU) to identify and refer eligible patients for clinical ...
Research Assistant 1
Montreal, QC · On-site
CA$30.54/hr
... monitor questionnaire completion (e.g. REDCap), and coordinate biospecimen collection. (v) Work jointly with the Clinical Research Unit (CRU) to identify and refer eligible patients for clinical ...
Research Assistant 1
Montreal, QC · On-site
CA$30.54/hr
... monitor questionnaire completion (e.g. REDCap), and coordinate biospecimen collection. (v) Work jointly with the Clinical Research Unit (CRU) to identify and refer eligible patients for clinical ...
Job Overview Perform monitoring and site management work to ensure that sites are conducting the ... Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i ...
Job Overview Perform monitoring and site management work to ensure that sites are conducting the ... Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i ...
Start-up Administrator
Montreal, QC · On-site
Monitor financial activity for clinical trials and ensure payments are received by the sponsor and ... Provide backup support to other administrative or research support staff within area of ...
Start-up Administrator
Montreal, QC · On-site
Monitor financial activity for clinical trials and ensure payments are received by the sponsor and ... Provide backup support to other administrative or research support staff within area of ...
Start-up Administrator
Montreal, QC · On-site
Monitor financial activity for clinical trials and ensure payments are received by the sponsor and ... Provide backup support to other administrative or research support staff within area of ...
Start-up Administrator
Montreal, QC · On-site
Monitor financial activity for clinical trials and ensure payments are received by the sponsor and ... Provide backup support to other administrative or research support staff within area of ...
An experienced Clinical Research Associate with a minimum of 2 years of on-site monitoring experience. * Knowledgeable in clinical trial processes, regulatory requirements, and ICH-GCP guidelines.
An experienced Clinical Research Associate with a minimum of 2 years of on-site monitoring experience. * Knowledgeable in clinical trial processes, regulatory requirements, and ICH-GCP guidelines.
... clinical research organisation united by a mission to bring new medicines and treatments to ... Monitor and track adherence and disclosures, * Budget closeout. Meeting Planning: * Organize ...
... clinical research organisation united by a mission to bring new medicines and treatments to ... Monitor and track adherence and disclosures, * Budget closeout. Meeting Planning: * Organize ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology
Kirkland, QC · On-site
Prepare monitoring reports following Standard Operating Procedures and timelines * Support ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology
Kirkland, QC · On-site
Prepare monitoring reports following Standard Operating Procedures and timelines * Support ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Quebec, QC · On-site
Prepare monitoring reports following Standard Operating Procedures and timelines * Support ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Quebec, QC · On-site
Prepare monitoring reports following Standard Operating Procedures and timelines * Support ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Laval, QC · On-site
Prepare monitoring reports following Standard Operating Procedures and timelines * Support ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Laval, QC · On-site
Prepare monitoring reports following Standard Operating Procedures and timelines * Support ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Kirkland, QC · On-site
Prepare monitoring reports following Standard Operating Procedures and timelines * Support ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Kirkland, QC · On-site
Prepare monitoring reports following Standard Operating Procedures and timelines * Support ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...
Clinical Research Monitor information
See Quebec salary details
$22.5K - $32K
4% of jobs
$41.1K is the 25th percentile. Wages below this are outliers.
$32K - $41.5K
22% of jobs
$41.5K - $51K
6% of jobs
$51K - $60.5K
6% of jobs
$60.5K - $70K
5% of jobs
The median wage is $78.7K / yr.
$70K - $79.5K
6% of jobs
$79.5K - $89K
5% of jobs
$89K - $98.5K
5% of jobs
$104.3K is the 75th percentile. Wages above this are outliers.
$98.5K - $108K
23% of jobs
$108K - $117.5K
9% of jobs
$117.5K - $127K
8% of jobs
$22.5K
$81K
$127K
How much do clinical research monitor jobs pay per year?
What is a clinical research monitor?
A clinical research monitor, also called a clinical research associate, oversees the operations of a clinical trial to ensure that it meets all safety and governmental regulations. As a clinical research monitor, your job duties include traveling to testing sites, inspecting the procedures, documenting results from the trial, and verifying that all collected data is accurate and verified. Your primary responsibility is to make sure the testing is conducted safely and within industry and governmental guidelines.
What are the key skills and qualifications needed to thrive as a clinical research monitor?
What are some common challenges clinical research monitors face when overseeing multiple study sites?
What is the difference between Clinical Research Monitor vs Clinical Research Associate?
| Aspect | Clinical Research Monitor | Clinical Research Associate |
|---|---|---|
| Certifications | Often required or preferred certifications like CCRP or CCRA | Similar certifications such as CCRP or CCRA are common |
| Work Environment | Monitoring visits at sites, reviewing data, ensuring compliance | Site visits, data collection, and regulatory documentation |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Pharmaceutical companies, CROs, biotech firms |
Both roles involve overseeing clinical trial activities, ensuring compliance, and maintaining data integrity. While the titles are often used interchangeably, the term 'Clinical Research Monitor' emphasizes the monitoring aspect, whereas 'Clinical Research Associate' may encompass broader responsibilities in clinical trial management. Both roles require similar certifications and work in comparable environments within the industry.
What does a clinical research monitor do in clinical research?
What are popular job titles related to Clinical Research Monitor jobs in Quebec?
For Clinical Research Monitor jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Clinical Research Monitor jobs in Quebec look for?
The top searched job categories for Clinical Research Monitor jobs in Quebec are:
What are popular job titles related to Clinical Research Monitor jobs in QC?
For Clinical Research Monitor jobs in QC, the most frequently searched job titles are:

Full-time
Medical, Dental, Vision, PTO
Re-posted 18 days ago
Altasciences rating
7.6
Based on 17 frontline employees who took The Breakroom Quiz
60th of 120 rated laboratories
Job description
Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Clinical Research Nurse will oversee the safety and consent of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
What You'll Do Here
Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records.
Ensure the confidentiality of clinical trial participants and sponsors is respected.
Perform clinical trial activities including but not limited to, continuous safety monitoring, safety assessments, Investigational Product (IP) administration and catheter installation.
Monitor, document and/or follow-up on participant adverse events.
Maintain and advocate a high level of patient care, quality, and safety within the department.
May assist in study related consenting with participant screenings.
Provide feedback, where necessary, to appropriate team members of study progress.
Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
May train employees on clinical trial activities associated to their job's needs.
Other tasks as assigned by management.
What You'll Need to Succeed
DEC from accredited Registered Nurse program required
Permit from the Ordre des infirmiers et infirmieres du Quebec (OIIQ) required.
Good communication in French and English.
Customer service focused.
Able to work in fast-paced environment.
Knowledge of the Microsoft suite
Excellent verbal and written communication skills.
Well-developed interpersonal skills are required.
Personal/professional integrity and proven discretion in handling confidential information.
Capable of managing multiple conflicting priorities.
Relevant industry experience a plus.
Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of Clinical Research Nurse including, but not limited to, for the following reasons:
The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.
What We Offer
Full time position (37,5 hours/week).
Availability every other weekend is required.
Day, evening or night shift (no shift rotation).
6 to 8 weeks of theory and practical training on the day shift.
On site position at our Montreal site (1200 Beaumont).
Accessible by public transportation (Metro L' Acadie), Free parking for employees.
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package Includes:
Health/Dental/Vision Insurance Plans
RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave
Employee Assistance & Telehealth Programs
Altasciences' Incentive Programs Include:
Training & Development Programs
Employee Referral Bonus Program
Annual Performance Reviews
#LI-JG1
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!
What Altasciences employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom