Freelance Clinical Research Associate (Dermatology) - Remote

Overview

The Contractual Clinical Research Associate (cCRA) will monitor the progress of clinical studies at investigative sites or remotely, ensuring compliance with protocols and regulatory requirements.

In Short

• Conduct site qualification, initiation, monitoring, and close-out visits.
• Participate in investigators’ meetings.
• Prepare site visit reports and follow-up letters.
• Build relationships with investigators and site staff.
• Perform source data verification and ensure study drug accountability.
• Work autonomously to meet quality standards.
• Focus on dermatology and develop expertise in this area.
• Travel to research sites approximately 65% of the time.
• Work in a mid-sized CRO where contributions are valued.
• Engage in other responsibilities as needed.

Requirements

• B.Sc. in a relevant field or equivalent experience.
• 3 years of clinical monitoring experience in the biotechnology or pharmaceutical industry.
• 1 year of experience in dermatology.
• Good knowledge of ICH/GCP standards.
• Strong verbal and written communication skills in English.
• Ability to prioritize assignments and work under pressure.
• Excellent judgement and problem-solving skills.
• Proficient in Microsoft Office.
• Experience in dermatology is an asset.

Benefits

• Stimulating work environment.
• Attractive advancement opportunities.
• Collaboration and innovation-focused culture.
• Equitable treatment and equal opportunity for all individuals.
• Accommodations for applicants with disabilities upon request.