Freelance Senior Clinical Research Associate - Remote

Overview

The Contractual Clinical Research Associate (cCRA) will monitor the progress of clinical studies at investigative sites or remotely, ensuring that 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

• Contractual position focusing on clinical monitoring in dermatology.
• Work autonomously to meet quality standards and deadlines.
• Conduct site qualification, initiation, monitoring, and close-out visits.
• Participate in investigators’ meetings and prepare site visit reports.
• Build relationships with investigators to achieve study objectives.
• Perform source data verification and ensure regulatory compliance.
• Travel to research sites approximately 65% of the time.
• Strong knowledge of ICH/GCP standards required.
• Excellent verbal and written communication skills in English.
• Experience in dermatology is an asset.

Requirements

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

Benefits

• Stimulating work environment with collaboration and innovation.
• Attractive advancement opportunities.
• Work with a team of driven colleagues.