CRA II - phase I ICON is a global healthcare intelligence and clinical research organisation united ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
CRA II - phase I ICON is a global healthcare intelligence and clinical research organisation united ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Job Summary 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 ...
Job Summary 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 ...
Job Summary 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 ...
Job Summary 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 ...
Job Summary 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 ...
Job Summary 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 ...
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)
Apercu du poste * L'ARC II est responsable de la surveillance des essais cliniques de phase I a IV ... Disponibilite pour des deplacements a hauteur de 65 a 70 % Clinical Research Associate II IQVIA is ...
Apercu du poste * L'ARC II est responsable de la surveillance des essais cliniques de phase I a IV ... Disponibilite pour des deplacements a hauteur de 65 a 70 % Clinical Research Associate II IQVIA is ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Apercu du poste * L'ARC II est responsable de la surveillance des essais cliniques de phase I a IV ... IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Apercu du poste * L'ARC II est responsable de la surveillance des essais cliniques de phase I a IV ... IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Quebec, QC · On-site
Apercu du poste * L'ARC II est responsable de la surveillance des essais cliniques de phase I a IV ... IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Quebec, QC · On-site
Apercu du poste * L'ARC II est responsable de la surveillance des essais cliniques de phase I a IV ... IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Laval, QC · On-site
Apercu du poste * L'ARC II est responsable de la surveillance des essais cliniques de phase I a IV ... IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ...
Attache de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology, IQVIA Biotech
Laval, QC · On-site
Apercu du poste * L'ARC II est responsable de la surveillance des essais cliniques de phase I a IV ... IQVIA Biotech is seeking an experienced Clinical Research Associate II (CRA II) with oncology ...
Associe(e) de recherche clinique (ARC) principal(e)/ Senior Clinical Research Associate, Sponsor ...
Quebec, QC · On-site
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Associe(e) de recherche clinique (ARC) principal(e)/ Senior Clinical Research Associate, Sponsor ...
Quebec, QC · On-site
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Associe(e) de recherche clinique (ARC) principal(e)/ Senior Clinical Research Associate, Sponsor ...
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Associe(e) de recherche clinique (ARC) principal(e)/ Senior Clinical Research Associate, Sponsor ...
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Associe(e) de recherche clinique (ARC) principal(e)/ Senior Clinical Research Associate, Sponsor ...
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Associe(e) de recherche clinique (ARC) principal(e)/ Senior Clinical Research Associate, Sponsor ...
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Associe(e) de recherche clinique (ARC) principal(e)/ Senior Clinical Research Associate, Sponsor ...
Quebec, QC · On-site
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Associe(e) de recherche clinique (ARC) principal(e)/ Senior Clinical Research Associate, Sponsor ...
Quebec, QC · On-site
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Associate, Global Markets
Montreal, QC · On-site
The Associate is expected to maximize profit based on customer flow and experience while minimizing ... I-star and our internal web-based research document database * Receive transaction and inspect form ...
Associate, Global Markets
Montreal, QC · On-site
The Associate is expected to maximize profit based on customer flow and experience while minimizing ... I-star and our internal web-based research document database * Receive transaction and inspect form ...
Associate, Global Markets
Montreal, QC · On-site
The Associate is expected to maximize profit based on customer flow and experience while minimizing ... I-star and our internal web-based research document database * Receive transaction and inspect form ...
Associate, Global Markets
Montreal, QC · On-site
The Associate is expected to maximize profit based on customer flow and experience while minimizing ... I-star and our internal web-based research document database * Receive transaction and inspect form ...
The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned. Assume line management responsibilities, as assigned. Act in ...
The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned. Assume line management responsibilities, as assigned. Act in ...
U.S. Tax, Senior Associate (Bilingual FR/EN)
CA$58K - CA$97K/yr
Tax research at the federal and state level. This could include drafting of memos and technical ... Preparation or review of other tax related calculations, i.e. IRC 382 or earnings and profit ...
U.S. Tax, Senior Associate (Bilingual FR/EN)
CA$58K - CA$97K/yr
Tax research at the federal and state level. This could include drafting of memos and technical ... Preparation or review of other tax related calculations, i.e. IRC 382 or earnings and profit ...
Accounting and Transaction Advisory Senior Associate (Bilingual FR/EN)
CA$58K - CA$97K/yr
Support our Deals teams with accounting implications on specific transactions (i.e.buy side, sell ... Research technical accounting matters as required by themanager * Work with the team and our ...
Accounting and Transaction Advisory Senior Associate (Bilingual FR/EN)
CA$58K - CA$97K/yr
Support our Deals teams with accounting implications on specific transactions (i.e.buy side, sell ... Research technical accounting matters as required by themanager * Work with the team and our ...
May document and/or report clinical trial related deviations (i.e. SOP, protocol). * Report, track ... The requirement to have study protocols, designs and clinical research documents written and ...
May document and/or report clinical trial related deviations (i.e. SOP, protocol). * Report, track ... The requirement to have study protocols, designs and clinical research documents written and ...
Research & Analysis - Responsible for conducting in-depth company, industry, and portfolio analysis ... Business Development Support - Play an integral role in the end-to-end processing of a loan (i.e ...
Research & Analysis - Responsible for conducting in-depth company, industry, and portfolio analysis ... Business Development Support - Play an integral role in the end-to-end processing of a loan (i.e ...
Research Associate I information
What is the difference between Research Associate I vs Research Associate II?
| Aspect | Research Associate I | Research Associate II |
|---|---|---|
| Required Credentials | Bachelor's degree in relevant field | Bachelor's or Master's degree, more experience |
| Work Environment | Entry-level research settings, laboratories | Similar environments, with increased responsibilities |
| Employer & Industry Usage | Common in biotech, pharma, academia | Same industries, higher expectations |
The main difference between Research Associate I and Research Associate II lies in experience and responsibility. Research Associate II typically requires more experience or advanced education and involves more complex tasks. Both roles are found in similar environments and industries, but Research Associate II often takes on greater responsibilities and may supervise junior staff.
How to become a research associate I?
What are the key skills and qualifications needed to thrive as a Research Associate I?
What does a Research Associate I do?
What are some common challenges faced by a Research Associate I, and how can they be addressed?

Full-time
Medical, Dental, Vision, Life, Retirement
Posted 5 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.
What You Will Do:
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports
Your Profile:
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.
Experience monitoring phase I studies required
Ability to work independently and collaboratively in a fast-paced environment.
Willingness to travel as required (approximately 60%)
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