Sign in
Profile
Library
Discovery
Jobs
Applications
Resources
Senior Manager, Submission Management Clinical Trials
Sign in to apply
Bristol Myers Squibb
50% onsite
7+ years regulatory submissions experience
Global cta dossier preparation
Eu ctis substantial modifications management
Skills & Requirements
Must-have
7+ years regulatory submissions experience
Global CTA dossier preparation
EU CTIS substantial modifications management
Health authority negotiation skills
Team leadership and mentoring
Nice-to-have
Continuous improvement initiative drive
Innovation in regulatory processes
Cross-functional stakeholder collaboration
Science or technology degree background
Key Requirements
BA/BS degree in science/technology field preferred
7+ years relevant regulatory submissions experience
Experience managing global clinical trial applications
Work Rights
Not specified
Tailored Resume
Sign in to tailor your resume
Cover Letter
Sign in to generate cover letter