Research Assistant (Assistant(e) de recherche) - RA

Join Centricity Research!

Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized integrated research organization (IRO) specializing in conducting clinical trials from phases I to IV across more than 35 therapeutic areas: hospital-based and ambulatory studies, pharmaceutical, biotech, and medical device trials.

About the Position

We are seeking a Research Assistant to support the conduct of clinical studies from start to finish.

This is a mobile position serving our Mirabel and Pointe-Claire sites. The selected candidate will work on-site five days a week and may be required to work at either site depending on study schedules and operational needs.

You will work closely with principal investigators, clinical research coordinators, and site teams to ensure the smooth conduct of studies, in compliance with protocols and regulatory requirements.

Essential Requirement: The candidate must have recent practical experience with blood draws and be able to perform them autonomously and safely upon starting the position. Blood draws are mandatory for this role.

Locations: Mirabel and Pointe-Claire, QC — mobile between the two sites

Hours: On-site, five days a week

Salary Range: $45,000 to $50,000 per year

This position is eligible for incentive pay.

Your Main Responsibilities

• Study Protocols and Safety: Perform activities in accordance with BPC (GCP), SOPs, protocols, and regulatory requirements. Ensure the safety of participants during all study activities.
• Recruitment and Enrollment: Participate in the recruitment, pre-screening, and enrollment of participants. Support the informed consent process and maintain complete and accurate documentation.
• Study Visit Execution: Perform blood draws required by protocols autonomously and safely. Conduct vital signs, ECGs, point-of-service tests, and other delegated clinical assessments. Collect, process, store, and ship biological specimens in accordance with protocols.
• Data Integrity and Compliance: Complete source documents and CRFs and keep the CTMS up-to-date. Report adverse events promptly in accordance with applicable procedures.
• Administrative and Site Support: Support the management and documentation of investigational products. Prepare monitoring visits and audits and maintain the ISF. Organize examination rooms and support daily site activities.
• Work at Mirabel or Pointe-Claire depending on study schedules and operational priorities.
• Collaborate effectively with teams at both sites.

You Might Be the Perfect Fit If You

• Hold a degree in a health, science, or research field, or have equivalent experience.
• Have recent practical experience with blood draws.
• Can perform blood draws autonomously and safely upon starting the position.
• Are available to work on-site five days a week.
• Are available and able to work at the Mirabel and Pointe-Claire sites as needed.
• Are comfortable with clinical tools and medical terminology.
• Demonstrate a strong attention to detail and excellent organizational skills.
• Communicate clearly and professionally.
• Can read and understand English.
• Are proficient with Microsoft Office.
• Work well in a team while demonstrating autonomy and initiative.
• Have experience in clinical research, which is a significant asset.
• Why Centricity Research?
• Our Mission

We bring people to scientific advances through cutting-edge research conducted in a deeply human environment.

Our Values

• Quality
• Kindness
• Be the Change
• One Team
• Grow for the Common Good
• Take Ownership

Benefits

• Health, dental, and vision insurance
• Enhanced PAE
• Flexible paid time off
• Continuing education reimbursement
• Employer-paid REER
• Ready to Apply?

We would be delighted to receive your application! Please note that this position is based on-site in Quebec, five days a week.

We are an equal opportunity employer and we foster a diverse and inclusive workplace.