Offer summary
Qualifications:
Bachelor's degree in relevant field, Minimum 3 years of IRT management experience, Knowledge of FDA regulations and GCP guidelines, Experience with EDC and eTMF systems, Attention to detail and project management skills.
Key responsabilities:
- Serve as a subject matter expert in IRT
- Lead IRT initiatives and ensure compliance
- Create training materials and resolve IRT issues
- Analyze IRT processes and propose enhancements
- Collaborate on demand planning for clinical trials