Offer summary
Qualifications:
MD, MB/BS or equivalent degree, Significant experience in pharmaceutical industry, Strong medical knowledge and clinical experience, Fluent in spoken and written English, Understanding of NDA submission process.Key responsabilities:
- Provide medical support for clinical trials
- Create clinical trial protocols and related documents
- Ensure study compliance with SOPs and GCP
- Serve as liaison between sponsor and departments
- Conduct PPD educational presentations for sites