Provide medical leadership to the study teams
Create clinical trial protocols while implementing the latest scientific information
Contribute to site selection
Review and approve study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs)
Ensure medical validity of each primary endpoint
Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP
Serve as chief liaison between sponsor and all PPD internal departments
Educate Investigator sites by delivering a protocol specific lab procedures presentation during investigator meeting

Medical Doctor, with a specialty in Pulmonology
1-2 years of industry experience in clinical development
Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine
Fluent in spoken and written English
Shown understanding and experience with NDA submission process
Shown understanding of regulatory guidelines for adverse event reporting
Strong communication & presentation skills and is a strong teammate

We provide our teams with the resources needed to achieve individual career goals
Join our colleagues in bringing our Mission to life
enabling our customers to make the world healthier, cleaner and safer.
Health insurance
Flexible working hours
Professional development opportunities

Medical Director – Pneumonologist

Key skills