Clinical Research jobs in Canada
Associé de recherche clinique, Télécommande– francophone (Canada), IQVIA Clinical Research Asso[...]
IQVIA
Senior Site Manager (Clinical Research Associate)
Johnson & Johnson
Associé de recherche clinique, – francophone (Canada), IQVIA Clinical Research Associate - Fren[...]
IQVIA
Research Nurse (Per Diem, Contract) - Brandon, Manitoba
Syneos Health, Inc.
Research & Database Coordinator (Rheumatology)
University of British Columbia
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Northern Lincolnshire and Goole NHS Foundation Trust
Sr. Clinical Trial Manager -Canada
Syneos Health, Inc.
MTA: MAT LEAVE Coverage in Ontario-Temp, FT (37.5h.w), $35.67 – $39.38/h, 315 bed facility-Ment[...]
Waypoint Centre for Mental Health Care
Connect with headhunters to apply for similar jobsClinical Trial Manager II
Syneos Health, Inc.
Join our Talent Pool - Clinical Research Associates (Canada)
Alimentiv
CRA II/ SrCRA, Sponsor Dedicated, Home based
Syneos Health, Inc.
Sr Clinical Research Associate - Sponsor Dedicated - Cardiology (Home-Based in Ontario)
Syneos Health, Inc.
Global Study Manager, Oncology R&D, Early Oncology Clinical - 12 Month Contract
AstraZeneca
Tenure Track Position in Clinical Psychology
New Mexico Behavioral Health Institute (NMBHI)
Join our Talent Pool - Project Management (Europe)
Alimentiv
Principal Medical Writer - Regulatory Submission Documents
Syneos Health, Inc.
Associé scientifique, Opérations de laboratoire / Associate Scientist, Laboratory Operations
IQVIA
Software QA Engineer/Ingénieur(e) QA logiciel
IQVIA
Principal Medical Writer - Submission Docs (2.5/2.7.2/2.7.3/2.7.4) - Oncology - Remote Based
Syneos Health, Inc.
Associate Site Manager (Clinical Research Associate) - Western Canada
Johnson & Johnson
Senior Cardiology CRA – Sponsor‑Dedicated, Remote, Ontario
Syneos Health, Inc.
Consultant en commerce de détail (Contrat)/ Retail Business Consultant (Contract)
IQVIA
Spécialiste en métrologie / Metrology Specialist
IQVIA
Associé de recherche clinique, Télécommande– francophone (Canada), IQVIA Clinical Research Asso[...]
Job summary
A leading clinical research organization in Montreal is seeking a Clinical Research Associate to monitor and manage clinical trials. Responsibilities include participating in investigator recruitment, ensuring regulatory compliance, and serving as the primary contact with investigators. The ideal candidate will hold a degree in life sciences or healthcare and have at least 4 years of experience in site monitoring. This role requires travel, with opportunities for career advancement and a competitive salary of up to $192,500 annually.
Benefits
Qualifications
- Minimum of four (4) years of experience in site monitoring/management.
- Experience in monitoring and/or coordinating clinical trials.
- Valid driver's license and ability to travel as required.
Responsibilities
- Participate in the investigator recruitment process.
- Collaborate with site staff to ensure regulatory compliance.
- Conduct study initiation and closure activities.
- Monitor clinical trials for adherence to good clinical practices.
- Serve as the primary contact between employer and investigators.
Skills
Education
Employer Industry: Clinical Research Services
- Salary up to $192,500.00 annually
- Opportunity for career advancement and growth within the organization
- Collaborative and supportive work environment
- Chance to work on innovative medical treatments that improve patient outcomes
- Involvement in diverse clinical trials across various phases
- Travel opportunities both domestically and internationally (approximately 65% to 85%)
- Participate in the investigator recruitment process and conduct on-site evaluation visits of potential investigators
- Collaborate with site staff to coordinate activities in preparation for study launches and ensure regulatory compliance
- Conduct study initiation and closure activities, including training site staff on study procedures and EDC systems
- Monitor clinical trials to ensure adherence to good clinical practices and validate source documentation
- Serve as the primary contact between the employer and investigators, ensuring timely communication and data transmission
- BS/BA/BSc (or equivalent) in a life sciences or healthcare field and a minimum of four (4) years of experience in site monitoring/management
- Mandatory experience in monitoring and/or coordinating clinical trials
- Excellent written and verbal communication skills
- Strong organizational and interpersonal skills with the ability to manage multiple priorities
- Valid driver's license and ability to travel as required
- Previous experience in a clinical research organization (CRO)
- Experience in leading project teams
- Working knowledge of budget management
- Familiarity with GCP/ICH guidelines and electronic data entry systems
- Ability to mentor and train other CRAs
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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.