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 productive relationships with investigators and site staff.
• Perform source data verification and ensure regulatory document collection.
• Work autonomously to meet quality standards and deadlines.
• 3 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.

Requirements

• B.Sc. in a relevant field or equivalent experience.
• 3 years of experience in biotechnology or CRO industry.
• At least 1 year of experience in dermatology.
• Ability to prioritize assignments and work under pressure.
• Excellent judgement and problem-solving skills.
• Proficient in Microsoft Office (Word, Excel, PowerPoint).

Benefits

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