Bilingual Clinical Research Associate II - Remote

Overview

The bilingual clinical research associate II (CRA II) will monitor the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

In Short

• Conducts site qualification, initiation, monitoring, and close-out visits for research sites.
• Participates in investigators’ meetings.
• Prepares site visit reports and follow-up letters to the investigator.
• Builds productive relationships with investigators and site staff.
• Performs source data verification and ensures study drug accountability.
• May be assigned other responsibilities based on experience.
• Requires strong communication skills in English.
• Travel to research sites approximately 65% of the time.
• Flexible work schedule.
• Full-time permanent position.

Requirements

• B.Sc. in a relevant field or nursing degree.
• 1-3 years experience in clinical monitoring.
• Experience in dermatology trials.
• Good knowledge of ICH/GCP standards.
• Excellent judgement and problem-solving skills.
• Strong knowledge of Microsoft Office.

Benefits

• Complete benefits (medical, dental, vision, RRSP).
• Ongoing learning and development opportunities.
• Option to work from home anywhere in Canada.
• Social activities and public transportation rebates.