Offer summary
Qualifications:
Bachelor's degree or equivalent, 5+ years of relevant experience, Strong leadership and mentorship skills, Extensive knowledge of clinical monitoring, Familiarity with ICH/GCP, FDA guidelines.
Key responsabilities:
- Oversee clinical operational and quality aspects of studies
- Coordinate team activities regarding project timelines and metrics
- Develop clinical tools and documentation
- Maintain communication with study sites to address issues
- Manage clinical resource allocation and performance monitoring