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Clinical research Jobs in Deux-Montagnes, QC

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Clinical research • deux montagnes qc

Last updated: 1 day ago
  • Promoted
Clinical Research Associate - Oncology - Sponsor Dedicated - Montreal or Quebec City

Clinical Research Associate - Oncology - Sponsor Dedicated - Montreal or Quebec City

ICON Strategic SolutionsGreater Montreal Metropolitan Area, Canada
Full-time
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
  • Promoted
Clinical Nurse

Clinical Nurse

Bien Chez SoiBeaconsfield, QC
CA$57.03–CA$60.70 hourly
Quick Apply
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
  • Promoted
Food research scientist

Food research scientist

JhubzDorval, QC, Canada
Permanent
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
  • Promoted
Food research scientist

Food research scientist

TechsoDorval, QC, Canada
Permanent
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
food research scientist

food research scientist

Repas WecookQC, CA
Full-time +1
Heures de travail : 40 hours per week.Biological and physical sciences.Fast moving consumer goods (FMCG).Participate in the commercialization of new products. Monitor and compile research results.Gov...Show moreLast updated: 10 days ago
  • Promoted
LIMS Clinical Studies Specialist

LIMS Clinical Studies Specialist

Planet TechnologyLaval, QC, Canada
Full-time
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
  • Promoted
Biostatisticien Senior FSP, Phase Tardive (Senior Biostatistician)

Biostatisticien Senior FSP, Phase Tardive (Senior Biostatistician)

IQVIA LLCKirkland, Montreal (administrative region), Canada
Full-time
Biostatisticien Senior FSP, Phase Tardive (Senior Biostatistician).Data Sciences Staffing Solutions, DS3, is a unit within IQVIA that provides our sponsors with fully embedded resources through a F...Show moreLast updated: 1 day ago
Research Advisor

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)

Academic Research Assistant (Mathematics)

OutlierLaval, Quebec, Canada
CA$30.00–CA$50.00 hourly
Full-time
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
  • Promoted
Clinical Vetterinary Assistant

Clinical Vetterinary Assistant

ITR Laboratories Canada Inc.Baie-D'Urfé, Quebec, Canada
Permanent
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
Research Assistant, R&D

Research Assistant, R&D

CIRION BioPharma ResearchLaval, Canada
CA$47,320.00–CA$87,887.80 yearly
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
Clinical Veterinarian

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
  • Promoted
Clinical Veterinarian

Clinical Veterinarian

Charles River LaboratoriesLaval, Canada
Full-time +1
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
Associé de recherche clinique, – francophone (Canada), IQVIA Clinical Research Associate - French speaking (Canada), IQVIA

Associé de recherche clinique, – francophone (Canada), IQVIA Clinical Research Associate - French speaking (Canada), IQVIA

IQVIAKirkland, Quebec, Canada
CA$47,320.00–CA$87,887.80 yearly
Full-time
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
Remote Data Research Coordinator

Remote Data Research Coordinator

FocusGroupPanelDollard-des-Ormeaux, Quebec, Canada
CA$250.00 daily
Remote
Part-time
About the Data Entry Research Participant position.We are looking for dependable, trustworthy individuals from various work experience backgrounds such as customer service, administrative assistant...Show moreLast updated: 30+ days ago
Scientist- Bioanalysis (LC-MS / MS)

Scientist- Bioanalysis (LC-MS / MS)

ITR Laboratories CanadaBaie d'urfé, QC, CA
CA$19.50 hourly
The Scientist will be experienced in research and development for Bioanalytical LC-MS / MS assays.They will need to develop innovative solutions to mass spectrometry challenges.They will troubleshoot...Show moreLast updated: 30+ days ago
Research Associate Analytical Chemistry

Research Associate Analytical Chemistry

Services de Gestion Quantum LtéeMontréal / Saint Laurent, Quebec, Canada
Full-time +1
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
Oncology Clinical Research Associate - Canada -

Oncology Clinical Research Associate - Canada -

ScimegaLaval, Quebec
CA$46,147.00 yearly
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
Research & Technology Engineering Program Manager

Research & Technology Engineering Program Manager

BombarbierDorval, Québec, CA, H4S 1Y9
CA$70,000.00–CA$120,000.00 yearly
When applicable, Bombardier promotes flexible and hybrid work policies.At Bombardier, we design, build and maintain the world’s peak-performing aircraft for the world’s most discerning people and b...Show moreLast updated: 30+ days ago
Intern, Research and Technology (Summer 2025)

Intern, Research and Technology (Summer 2025)

BombardierDorval, QC
Full-time
Innovation is in our DNA… is it in yours?.Bombardier is a global leader in aviation, creating innovative and game-changing planes. Our products and services provide world-class experiences that set ...Show moreLast updated: 7 days ago
Clinical Research Associate - Oncology - Sponsor Dedicated - Montreal or Quebec City

Clinical Research Associate - Oncology - Sponsor Dedicated - Montreal or Quebec City

ICON Strategic SolutionsGreater Montreal Metropolitan Area, Canada
1 day ago
Job type
  • Full-time
Job description

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

  • Primary 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.)
  • What do you need to have?

  • 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.
  • 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

  • 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
  • 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.