Clinical research associate Jobs in Deux-Montagnes, QC
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Clinical research associate • deux montagnes qc
Last updated: 1 day ago
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Works on multiple trials within Oncology.Demonstrated leader...Show moreLast updated: 1 day ago
Description du poste Infirmier(ère).PLACEMENT SOINS SANTÉ ( filiale de BIEN CHEZ SOI).Planifier et évaluer les soins à donner.
Eacute;valuer la condition physique et ment...Show moreLast updated: 30+ days ago
Get AI-powered advice on this job and more exclusive features.Bachelor's degree in Food Science or related field.Fast moving consumer goods (FMCG).
Participate in the commercialization of new produc...Show moreLast updated: 1 day ago
Biological and physical sciences.Fast moving consumer goods (FMCG).Participate in the commercialization of new products.Monitor and compile research results.
Government regulations control.Industria...Show moreLast updated: 1 day ago![Associé(e), Recherche sur les résultats qualitatifs, Mesure de la qualité / Solutions axées sur l[...]](https://cdn-dynamic.talent.com/ajax/img/get-logo.php?empcode=jvers-jobboards-ca&empname=IQVIA%20Argentina)
Associé(e), Recherche sur les résultats qualitatifs, Mesure de la qualité / Solutions axées sur le patient / .Associate, Qualitative Outcomes Research, QualityMetric / Patient Centered Solutions.L’assoc...Show moreLast updated: 1 day ago
LIMS Clinical Studies Specialist – (Full-time) – Onsite – Quebec Canada.Contract Research Organization seeks a full-time onsite LIMS Clinical Studies Specialist with 2+ years’ experience working wi...Show moreLast updated: 16 days ago
Outlier helps the world’s most innovative companies improve their AI models by providing human feedback.Are you an experienced Mathematics expert who would like to lend your expertise to train AI m...Show moreLast updated: 6 days ago
At ITR Laboratories Canada INC Our Mission is to bring new medicines to the world which relieve patients suffering from serious diseases.
ITR Laboratories Canada has been servicing the pharmaceut...Show moreLast updated: 30+ days ago
Experience : 3 years to less than 5 years.Biological and physical sciences.Fast moving consumer goods (FMCG).Participate in the commercialization of new products.
Monitor and compile research results...Show moreLast updated: 6 days ago
Description Research Assistant, R&D (RH2024-003)Location : Laval, Canada CIRION BioPharma Research is looking for a Research Assistant.
Under the supervision of the Director, Research and Development...Show moreLast updated: 30+ days ago
A career as an Associate in the Wealth Management team at National Bank, will give you the opportunity to show your ability to work in synergy with clients and colleagues.In this role, you will hel...Show moreLast updated: 28 days ago
Remote Telecommute Work From Home Job Description : .We are looking for remote, telecommuting candidates from all types of work backgrounds and skill levels to join us.
This is a flexible, work from h...Show moreLast updated: 30+ days ago
Participates in the preparation and execution of Phase I to IV clinical trials.Oversees the progress of clinical investigations by conducting interim site assessment, initiation, and closure visits...Show moreLast updated: 30+ days ago
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies.
When you join our family, you will have a significant i...Show moreLast updated: 27 days ago
NOTE-MUST DRIVE as the shift starts Early Morning.Arrow Workforce Solutions now hiring Warehouse Associates for Distribution Centre in .
We offer full-time / part time hours as per business needs...Show moreLast updated: 9 days ago
Position : Research Associate - Analytical ChemistryLocation : Saint-Laurent, full-time work on site Salary : Flexible according to experience Job Type : 9-month contract Are you passionate about contr...Show moreLast updated: 4 days ago
Under the direction of the Director, Clinical and Scientific Affairs, the CTL is responsible for execution of clinical trials, from the site selection, start-up and enrollment phases up to the stud...Show moreLast updated: 30+ days ago
Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994.For over 25 years, we have developed an expertise in the development and manufacturing of non-ster...Show moreLast updated: 30+ days ago
- Promoted
Clinical Research Associate - Oncology - Sponsor Dedicated - Montreal or Quebec City
ICON Strategic SolutionsGreater Montreal Metropolitan Area, CanadaFull-time
- Promoted
Clinical Nurse
Bien Chez SoiBeaconsfield, QCCA$57.03–CA$60.70 hourly
Quick Apply
- Promoted
Food research scientist
JhubzDorval, QC, CanadaPermanent
- Promoted
Food research scientist
TechsoDorval, QC, CanadaPermanent
- Promoted
Associé(e), Recherche sur les résultats qualitatifs, Mesure de la qualité / Solutions axées sur l[...]
IQVIA ArgentinaKirkland, Montreal (administrative region), CanadaFull-time
- Promoted
LIMS Clinical Studies Specialist
Planet TechnologyLaval, QC, CanadaFull-time
Research Advisor
Cuso InternationalLaval, QC, CA This Volunteer Placement is Located in : .Please submit a Spanish Resume and Statement of Interest.Eligibility : Open to Canadian Citizens and Permanent Residents of Canada only.This is your opportuni...Show moreLast updated: 30+ days ago
- Promoted
Academic Research Assistant (Mathematics)
OutlierLaval, Quebec, CanadaCA$30.00–CA$50.00 hourly
Full-time
- Promoted
Clinical Vetterinary Assistant
ITR Laboratories Canada Inc.Baie-D'Urfé, Quebec, CanadaPermanent
Food research scientist
Repas WecookDorval, QC, CAFull-time +1
Research Assistant, R&D
CIRION BioPharma ResearchLaval, CanadaCA$47,320.00–CA$87,887.80 yearly
- Promoted
Associate
National BankLanaudière-Nord (Saint-Esprit), CanadaFull-time
Clinical Veterinarian
Charles River Laboratories, Inc.Montreal (Senneville), Queb, CA For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies.
When you join our family, you will have a significant i...Show moreLast updated: 27 days ago
Work-at-Home Data Research Associate
FocusGroupPanelLaval, Quebec, CanadaRemote
Part-time
Associé de recherche clinique, – francophone (Canada), IQVIA Clinical Research Associate - French speaking (Canada), IQVIA
IQVIAKirkland, Quebec, CanadaCA$47,320.00–CA$87,887.80 yearly
Full-time
- Promoted
Clinical Veterinarian
Charles River LaboratoriesLaval, CanadaFull-time +1
- Promoted
Warehouse Associate
Arrow Workforce SolutionsMirabel, QC, CanadaCA$19.16 hourly
Full-time +1
Research Associate Analytical Chemistry
Services de Gestion Quantum LtéeMontréal / Saint Laurent, Quebec, CanadaFull-time +1
Oncology Clinical Research Associate - Canada -
ScimegaLaval, QuebecCA$46,147.00 yearly
- Promoted
Product Development Associate
Groupe ParimaLaval, QuebecQuick Apply
Clinical Research Associate - Oncology - Sponsor Dedicated - Montreal or Quebec City
ICON Strategic SolutionsGreater Montreal Metropolitan Area, Canada1 day ago
Job type
- Full-time
Job descriptionPrimary interfaces : Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Other Interfaces : Study Responsible Physician, Regional Quality and Compliance. Manager / Specialist, Local Drug Safety Officer (where required) and Site Manager team; Investigators and their delegates at site (trial personnel including study coordinators, pharmacists, etc.) Have a minimum of a B.S., R.N., or equivalent degree, preferably in Biological Sciences Must be located in Canada Will work on US remote monitoring only Have a minimum of 2-5 years’ experience in monitoring pharmaceutical industry clinical trials Have a minimum of 1-2 years' experience monitoring Oncology trials Knowledge of several therapeutic areas Analytical / risk-based monitoring experience is an asset Ability to actively drive patient recruitment strategies at assigned sites Ability to partner closely with investigator and site staff to meet all of our study timelines Ability to operate and use various systems and databases (e.g. CTMS, EDC, eTMF, various dashboards / metrics, IWRS, safety reporting). Possess strong communication and influencing skills to effectively manage study sites both remotely and face to face. Strong team member and self-starter with the ability to work independently. Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements. To qualify, applicants must be legally authorized to work in Canada, and should not require, now or in the future, sponsorship for employment visa status. Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What will you be doing?
- Works on multiple trials within Oncology
- Demonstrated leadership, through involvement in specific initiatives when needed, and / or SME to systems and / or processes
- Mentors / coaches junior flex team
- Acts as Lead SM-training other SMs on study
- Develops site start up documents for studies including SIV agenda
- Provides SM “voice” when reviewing study documents (e.g. Monitoring Guidelines)
- Represents LTMs or SMs on SMTs / meetings
- Takes over LTM role reports review (SQV, SMV, SCV) for sites assigned to other SMs from the same trial
- Supports country budget development and / or contract negotiation in liaison with CCS colleagues
- Assists with ASV
- Metrics / KPIs : Metrics / KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document.
Interfaces – Primary / Other
What do you need to have?
What ICON Can Offer You
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our Benefits Examples Include
Visit our careers website to read more about the benefits of working at ICON :
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.