Clinical Research Technician conducting participant - facing clinical trial activities at Altasciences’ Montreal site. Handling samples, safety measurements, IP administration, and questionnaires.
About the role
- Clinical Research Associate II conducting onsite monitoring, CRF review, and site management for PSI, a contract research organization. Supporting clinical study startup, feasibility, and regulatory submissions.
Responsibilities
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup (if applicable)
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
Requirements
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in North America
- Experience in all types of monitoring visits in Phase II and/or III
- Full working proficiency in English and French
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver’s license
Benefits
- Employees can work remotely
- Opportunity to further develop skills
- Opportunity to widen therapeutic area experience
- Opportunity to become an expert in clinical research
Job title
Job type
Experience level
Salary
Degree requirement
Location requirements
Report this job
Found something wrong with the page? Please let us know by submitting a report below.
Clinical Research Nurse overseeing participant safety, consent, and clinical procedures for Altasciences clinical trials. Maintaining protocol compliance, safety equipment, and adverse - event documentation.
Clinical Research Associate monitoring sponsor - dedicated clinical trials for ICON, a global clinical research organization. Ensuring protocol compliance, data integrity, and patient safety.
Home - based Clinical Research Associate conducting site visits and monitoring clinical trials for Medpace, a full - service CRO. Supporting biotechnology, pharmaceutical, and medical device development.
Clinical Scientist designing trials, analyzing data, and supporting regulatory submissions at ICON, a global clinical research organization advancing new therapies.
Senior Clinical Research Associate overseeing clinical trial sites for Novo Nordisk, a pharmaceutical company developing treatments for chronic diseases. Ensuring compliant monitoring, patient safety, data integrity and timely study execution.
Clinical Research Associate monitoring clinical trials for pharmaceutical and biotech clients. Ensuring site compliance, data accuracy, essential documentation, and audit readiness across Alberta.
Canada - based Gastroenterologist serving as PSI Medical Monitor. Providing medical and safety oversight across global clinical studies and supporting trial teams, sponsors, and regulators.
Senior Clinical Research Associate monitoring oncology clinical trials for ICON in Eastern Canada. Managing sites, compliance, data integrity, and sponsor - dedicated trial operations.
Bilingual French Clinical Research Associate monitoring clinical trials for pharmaceutical and biotech sponsors. Ensuring site compliance, data integrity and audit readiness across remote and on - site visits.