Offer summary
Qualifications:
MD, MB/BS or equivalent degree, Board certified in Cardiology, Experience in pharmaceutical industry and clinical trials, Fluent in English (spoken and written), Understanding of NDA submission process.
Key responsabilities:
- Provide medical support for clinical trials and safety evaluation
- Create and approve clinical trial protocols and necessary documents
- Ensure medical monitoring and subject safety during studies
- Serve as liaison between sponsor and internal departments
- Educate site investigators and ensure compliance with SOPs