Freelance Clinical Research Associate (Dermatology) - Remote

Overview

The Freelance Clinical Research Associate (cCRA) will monitor clinical studies in dermatology, ensuring compliance with protocols and regulatory standards.

In Short

• Monitor progress of clinical studies at investigative sites or remotely.
• Ensure clinical trials are conducted per protocols and regulations.
• Conduct site qualification, initiation, monitoring, and close-out visits.
• Prepare site visit reports and follow-up communications.
• Build relationships with investigators and site staff.
• Perform source data verification and ensure regulatory compliance.
• Work autonomously to meet quality standards and deadlines.
• 3 years of clinical monitoring experience required.
• 1 year of dermatology experience preferred.
• Travel to research sites approximately 65% of the time.

Requirements

• B.Sc. in a relevant field or equivalent experience.
• Good knowledge of ICH/GCP standards.
• Strong verbal and written communication skills in English.
• Ability to prioritize assignments and work under pressure.
• Excellent judgment and problem-solving skills.
• Proficient in Microsoft Office.

Benefits

• Work with a collaborative and innovative team.
• Opportunities for professional advancement.
• Equitable treatment and accommodations for applicants with disabilities.