Responsibilities
- Oversee and manage the advancement of clinical trials at investigative locations.
- Ensure trials are executed, documented, and reported in alignment with study protocols, standard operating procedures, ICH-GCP guidelines, and relevant regulatory requirements.
- Organize and coordinate all activities essential for study setup and ongoing monitoring.
- Identify and evaluate potential investigators for study participation.
- Support the development and preparation of regulatory documentation for submissions.
- Perform pre-study assessments and site initiation visits to ensure readiness.
Work Arrangement
Remote — Turkey
