Clinical Research Associate II, Dermatology & Rheumatology - Remote

Overview

The clinical research associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure 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.
• Requires 2-5 years of experience in clinical monitoring.
• Good knowledge of ICH/GCP standards.
• Strong verbal and written communication skills in English.
• Travel to research sites approximately 65% of the time.
• Permanent full-time position with benefits.

Requirements

• B.Sc. in a field relevant to clinical research or equivalent experience.
• 2-5 years experience in the biotechnology, pharmaceutical, or CRO industry.
• Experience in dermatology is an asset.
• Ability to prioritize assignments and work under pressure.
• Excellent judgement and problem-solving skills.

Benefits

• Permanent full-time position.
• Benefits.
• 401K.
• Ongoing learning and development.