Senior Clinical Research Associate - Cardio Device - Canada ICON is a global healthcare ... Ability to work independently and manage multiple priorities in a dynamic environment. * A well ...
Senior Clinical Research Associate - Cardio Device - Canada ICON is a global healthcare ... Ability to work independently and manage multiple priorities in a dynamic environment. * A well ...
Senior Clinical Research Associate
Montreal, QC · On-site +1
Senior Clinical Research Associate - Home-Based (CANADA) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
Senior Clinical Research Associate
Montreal, QC · On-site +1
Senior Clinical Research Associate - Home-Based (CANADA) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
Clinical Research Associate
Montreal, QC · On-site
Clinical Research Associate - Montreal, Canada - Diabetes and Obesity ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...
Clinical Research Associate
Montreal, QC · On-site
Clinical Research Associate - Montreal, Canada - Diabetes and Obesity ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...
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 ...
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) at Worldwide, you will find yourself working alongside ... Responsible for managing the research activities at sites participating in Worldwide's clinical ...
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside ... Responsible for managing the research activities at sites participating in Worldwide's clinical ...
Clinical Research Associate 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 ...
Clinical Research Associate 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 ...
About The Role The Lead Clinical Research Associate (Lead CRA/LCRA) is responsible for overseeing ... Collaborating with the Data Management team to oversee SDV progress, query resolution, and timely ...
About The Role The Lead Clinical Research Associate (Lead CRA/LCRA) is responsible for overseeing ... Collaborating with the Data Management team to oversee SDV progress, query resolution, and timely ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in ...
Opportunity for CRA leadership positions - Lead CRA, CRA Manager * Many additional perks unmatched ... At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; * Bilingual in ...
Positions available: 1 (remote based, Canada ) Must be fluent in English and French Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include ...
Positions available: 1 (remote based, Canada ) Must be fluent in English and French Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include ...
Positions available: 1 (remote based, Canada ) Must be fluent in English and French Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include ...
Positions available: 1 (remote based, Canada ) Must be fluent in English and French Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include ...
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i ...
Manage the progress of assigned studies by tracking regulatory submissions and approvals ... Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i ...
Research Associate
CA$35.37/hr
Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ... Must be able to manage a diverse set of obligations on a daily basis with rapidly changing demands ...
Research Associate
CA$35.37/hr
Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ... Must be able to manage a diverse set of obligations on a daily basis with rapidly changing demands ...
Research Associate
CA$35.37/hr
Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ... Must be able to manage a diverse set of obligations on a daily basis with rapidly changing demands ...
Research Associate
CA$35.37/hr
Research Associate - Canada Excellence Research Chair in Metabolism and the Brain (CERC M&B ... Must be able to manage a diverse set of obligations on a daily basis with rapidly changing demands ...
The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good ... Capable of managing multiple conflicting priorities. * Relevant industry experience a plus.
The Clinical Research Nurse will execute tasks performed in compliance with study protocol, Good ... Capable of managing multiple conflicting priorities. * Relevant industry experience a plus.
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 ...
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 ...
Disponibilite pour des deplacements a hauteur de 65 a 70 % Clinical Research Associate II IQVIA is ... You will manage site activities from start-up through close-out. Key Responsibilities * Conduct ...
Disponibilite pour des deplacements a hauteur de 65 a 70 % Clinical Research Associate II IQVIA is ... You will manage site activities from start-up through close-out. Key Responsibilities * Conduct ...
Clinical Research Associate Manager information
What are the key skills and qualifications needed to thrive as a Clinical Research Associate Manager, and why are they important?
What is a Clinical Research Associate Manager?
What are some common challenges faced by Clinical Research Associate Managers when overseeing multiple clinical trials simultaneously?

Full-time
Medical, Dental, Vision, Life, Retirement
Posted 8 days ago
Job description
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, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Senior Clinical Research Associate - Cardio
To support 1study in the cardiovascular/electrophysiology medical device space. Indication is A-fib.
Candidates must have complex cardiac experience within the past 5 years, preferably in electrophysiology and / or devices.
3 years of monitoring experience required.
A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
Candidates must have/ be:
In-depth knowledge of FDA regulations and ICH/GCP guidelines.
Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
Fluent in French and English.
Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.
Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.
Ability to work independently and manage multiple priorities in a dynamic environment.
A well-executed plan for communication with the study teams and sites.
Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports.
Located in the Montreal area. Ability to cover up to 60% regional travel.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.
Are you a current ICON Employee? Please click here to apply