We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside ...
Associate Director, Operations - Clinical Assessment Technologies (CAT) - US/Canada - Remote
Quebec, QC · Remote
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best ...
Associate Director, Operations - Clinical Assessment Technologies (CAT) - US/Canada - Remote
Quebec, QC · Remote
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best ...
... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ... In-depth knowledge ofICH GCP,clinicaltrialsand the critical elements for success in clinical trials
... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ... In-depth knowledge ofICH GCP,clinicaltrialsand the critical elements for success in clinical trials
Senior Clinical Research Associate
Medical
Dental
Vision
Life
Retirement
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
Medical
Dental
Vision
Life
Retirement
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
Medical
Dental
Vision
Life
Retirement
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
Medical
Dental
Vision
Life
Retirement
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 ...
Clinical research associate II
Montreal, QC · On-site
Medical
Dental
Vision
Life
Retirement
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Clinical research associate II
Montreal, QC · On-site
Medical
Dental
Vision
Life
Retirement
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Bilingual Clinical Research Associate (CRA) - Montreal
Quebec, QC · Hybrid
Medical
Retirement
PTO
Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our ... Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ...
Bilingual Clinical Research Associate (CRA) - Montreal
Quebec, QC · Hybrid
Medical
Retirement
PTO
Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our ... Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ...
Bilingual Clinical Research Associate (CRA) - Montreal
Montreal, QC · Hybrid
Medical
Retirement
PTO
Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our ... Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ...
Bilingual Clinical Research Associate (CRA) - Montreal
Montreal, QC · Hybrid
Medical
Retirement
PTO
Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our ... Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ...
Bilingual Clinical Research Associate (CRA) - Montreal
Montreal, QC · Hybrid
Medical
Retirement
PTO
Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our ... Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ...
Bilingual Clinical Research Associate (CRA) - Montreal
Montreal, QC · Hybrid
Medical
Retirement
PTO
Job Summary Medpace is growing quickly and we are seeking a Clinical Research Associate to join our ... Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ...
Directeur medical adjoint-Neurologie / Associate Medical Director-Neurology(CAN)
Montreal, QC · On-site
... clinical trials to bring life-changing therapies to patients in need across the globe. Nous ... As an Associate Medical Director at Allucent, you are responsible for working independently to ...
Directeur medical adjoint-Neurologie / Associate Medical Director-Neurology(CAN)
Montreal, QC · On-site
... clinical trials to bring life-changing therapies to patients in need across the globe. Nous ... As an Associate Medical Director at Allucent, you are responsible for working independently to ...
Directeur medical adjoint-oncologie/ Associate Medical Director-Oncology (CAN)
Montreal, QC · On-site
... clinical trials to bring life-changing therapies to patients in need across the globe. Nous ... As an Associate Medical Director at Allucent, you are responsible for working independently to ...
New
Directeur medical adjoint-oncologie/ Associate Medical Director-Oncology (CAN)
Montreal, QC · On-site
... clinical trials to bring life-changing therapies to patients in need across the globe. Nous ... As an Associate Medical Director at Allucent, you are responsible for working independently to ...
New
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology
Kirkland, QC · On-site
Disponibilite pour des deplacements a hauteur de 65 a 70 % Clinical Research Associate II IQVIA is ... Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology
Kirkland, QC · On-site
Disponibilite pour des deplacements a hauteur de 65 a 70 % Clinical Research Associate II IQVIA is ... Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance ...
CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada
Montreal, QC · Remote
WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon ...
CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada
Montreal, QC · Remote
WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Kirkland, QC · On-site
IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ... Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Kirkland, QC · On-site
IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ... Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Laval, QC · On-site
IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ... Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Laval, QC · On-site
IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ... Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Quebec, QC · On-site
IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ... Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Quebec, QC · On-site
IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ... Overview The CRA II is responsible for monitoring Phase I-IV clinical trials to ensure compliance ...
Study Start Up CRA
Montreal, QC · On-site
Medical
Dental
Vision
Life
Retirement
Clinical Research Associate (Study Start Up) ICON is a global healthcare intelligence and clinical ... trials in the country in accordance with monitoring procedures and processes following ICH.GCP ...
Study Start Up CRA
Montreal, QC · On-site
Medical
Dental
Vision
Life
Retirement
Clinical Research Associate (Study Start Up) ICON is a global healthcare intelligence and clinical ... trials in the country in accordance with monitoring procedures and processes following ICH.GCP ...
Summary Reporting to the Associate Director, Client Services, the Proposal Specialist will prepare ... stage clinical trials. The Company operates globally with facilities located in Canada, USA ...
Quick apply
Summary Reporting to the Associate Director, Client Services, the Proposal Specialist will prepare ... stage clinical trials. The Company operates globally with facilities located in Canada, USA ...
Scientist, R&D Proteomics
Montreal, QC · On-site
Train Research Associates on sample preparation and analytical techniques * Provide scientific ... stage clinical trials. The Company operates globally with facilities located in Canada, USA ...
Quick apply
Scientist, R&D Proteomics
Montreal, QC · On-site
Train Research Associates on sample preparation and analytical techniques * Provide scientific ... stage clinical trials. The Company operates globally with facilities located in Canada, USA ...
Clinical Trials Associate information
See Quebec salary details
$22.60 - $25.98
20% of jobs
$25.98 - $29.37
3% of jobs
$29.72 is the 25th percentile. Wages below this are outliers.
$29.37 - $32.76
13% of jobs
The median wage is $35.25 / hr.
$32.76 - $36.15
18% of jobs
$39.32 is the 75th percentile. Wages above this are outliers.
$36.15 - $39.53
22% of jobs
$39.53 - $42.92
4% of jobs
$42.92 - $46.31
0% of jobs
$46.31 - $49.69
0% of jobs
$49.69 - $53.08
5% of jobs
$53.08 - $56.47
6% of jobs
$56.47 - $59.86
8% of jobs
$22
$39
$59
How much do clinical trials associate jobs pay per hour?
What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?
What do I need to be a clinical trials associate?
What are some common challenges faced by clinical trials associates, and how can they be managed effectively?
What is the difference between Clinical Trials Associate vs Clinical Research Coordinator?
| Aspect | Clinical Trials Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often in life sciences; certifications like ACRP or SOCRA are common | Bachelor's degree in health sciences or related field; certifications like CCRP are advantageous |
| Work Environment | Typically works in clinical trial sites, pharmaceutical companies, or CROs | Works directly at clinical sites, hospitals, or research centers |
| Job Focus | Supports trial setup, data entry, and regulatory compliance | Manages patient recruitment, scheduling, and data collection |
While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.
What is a clinical trials associate?

Senior Clinical Research Associate (Bilingual) - Oncology - Canada (Remote)
Quebec, QC
Full-time
Re-posted 4 days ago
Job description
Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!
What Clinical Operations does at Worldwide
At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.
Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.
We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!
What you will do
Responsible for managing the research activities at sites participating in Worldwide's clinical research projects
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect 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
Conduct study initiation visits (SIVs)
While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
What you will bring to the role
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to detail
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience
5+ years of experience as a Clinical Research Associate
4-year universitydegree OR Nursing Degree
Experience in Oncology is required
Fluent in written and verbal English and French is required
Candidates must reside in Canada
Willingness to travel regionally required
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
About Worldwide Clinical Trials
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Durham, NC, US
Year founded
1986