Contractual Clinical Research Associate (CRA) - Dermatology - Remote

Overview

The Contractual Clinical Research Associate (cCRA) 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

• 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 regulatory document collection.
• Work autonomously to meet quality standards and deadlines.
• Focus on dermatology as a therapeutic area.
• 3 years of experience in clinical monitoring.
• Good knowledge of ICH/GCP standards.
• Strong verbal and written communication skills in English.

Requirements

• B.Sc. in a relevant field, nursing degree, or equivalent experience.
• 3 years of clinical monitoring experience in biotech or CRO.
• At least 1 year of experience in dermatology.
• Strong judgment and problem-solving skills.
• Excellent knowledge of Microsoft Office.
• Ability to prioritize assignments and work under pressure.

Benefits

• Work with a collaborative and innovative team.
• Attractive advancement opportunities.
• Stimulating work environment.