Contractual Clinical Research Associate (CRA) in 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

• Conducts site qualification, initiation, monitoring, and close-out visits for research sites.
• Participates in investigators’ meetings.
• Prepares site visit reports and follow-up letters to the investigator.
• Builds productive relationships with investigators and site staff.
• Performs source data verification and ensures regulatory document collection is adequate.
• Requires 3 years of experience in clinical monitoring and 1 year in dermatology.
• Good knowledge of ICH/GCP standards is essential.
• Strong verbal and written communication skills in English are required.
• Travel to research sites approximately 65% of the time.
• Excellent knowledge of Microsoft Office is necessary.

Requirements

• B.Sc. in a field relevant to clinical research or nursing degree.
• 3 years of experience in the biotechnology or pharmaceutical industry.
• At least 1 year of experience in dermatology.
• Ability to work autonomously and meet quality standards.
• Excellent judgement and problem-solving skills.
• Ability to prioritize different assignments and work under pressure.

Benefits

• Work with a collaborative and innovative team.
• Stimulating work environment with advancement opportunities.
• Contribution to impactful clinical research in dermatology.