Clinical Research Associate II, Dermatology & Rheumatology - Remote

Overview

The 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 adequate data collection.
• May be assigned other responsibilities based on experience.

Requirements

• B.Sc. in a field relevant to clinical research or equivalent experience.
• 2-5 years of experience in conducting on-site clinical monitoring.
• Good knowledge of ICH/GCP standards and regulatory requirements.
• Strong verbal and written communication skills in English.
• Ability to prioritize assignments and work under pressure.
• Excellent judgement and problem-solving skills.
• Travel to research sites approximately 65% of the time.
• Excellent knowledge of Microsoft Office.
• Experience in dermatology is an asset.

Benefits

• Permanent full-time position.
• Flexible schedule.
• Home-based traveling position.
• Ongoing learning and development.