Stay current on scientific, regulatory, and operational aspects of assigned projects.
Conduct site evaluation and initiation visits; obtain pre-study docs for start-up.
Train site staff in study procedures.
Perform periodic monitoring visits and generate monitoring reports; review CRFs.
Perform source data verification and review of clinical data; resolve data queries.
Coordinate with site staff on safety reporting (AEs/SAEs/SUSARs) and follow-up.

🎯 Requirements

University degree in scientific, medical or paramedical disciplines.
Proven CRA experience with on-site monitoring.
Experience in Dermatology studies.
Strong knowledge of clinical trial operations, GCP/ICH.
Fluent in English and local languages.
Willingness to travel.

Apply on employer's website

This employer gathers applications via their own applicant tracking system.

You will be redirected to an external application form.

Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Healthcare Jobs. Just set your preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.

Activate JobCopilot