Offer summary
Qualifications:
Terminal scientific degree or Master's in Nursing with APRN licensure, Minimum 1 year of relevant experience in respiratory clinical trials or pharmaceutical industry, Strong familiarity with clinical research and study site logistics, Fluency in English and local language required, Knowledge of FDA compliance, GCP guidance, and regulatory requirements.
Key responsabilities:
- Develop and manage relationships with key sites and experts
- Provide medical and scientific support and presentations
- Support recruitment strategies and site performance
- Respond to site requests and feedback in a compliant manner
- Represent the Company professionally at meetings