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 according to the protocol 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 compliance.
• Travel to research sites approximately 65% of the time.
• Work in a mid-sized CRO environment.
• Focus on dermatology expertise.
• Meet quality standards and deadlines autonomously.

Requirements

• B.Sc. in a relevant field or nursing degree.
• 3 years of clinical monitoring experience.
• 1 year of experience in dermatology.
• Good knowledge of ICH/GCP standards.
• Strong verbal and written communication skills in English.
• Ability to prioritize assignments under pressure.
• Excellent judgment and problem-solving skills.
• Proficient in Microsoft Office.

Benefits

• Stimulating work environment.
• Attractive advancement opportunities.
• Collaboration and innovation-focused culture.
• Equal opportunity and accommodations for applicants with disabilities.