Sr Reg Affairs Spec
Core
Senior Regulatory Affairs Specialist leading global regulatory strategies and submissions for Phase 1-4 clinical trials.
Role type
Senior IC regulatory affairs specialist (clinical trials)
Builds
Global regulatory submissions and strategies for clinical trials
Domain
Life sciences / Clinical research / Regulatory affairs
Required skills
Global regulatory submissions preparation, Clinical trial document review, Scientific literature assessment, Project team management, Regulatory strategy coordination
Preferred skills
Bid defense meeting experience
Technologies
Microsoft Word, Excel, PowerPoint
Responsibilities
Lead discussions and coordinate regulatory strategies globally, Act as liaison with internal and external clients, Arrange and lead client and regulatory agency meetings, Support business development initiatives, Participate in launch and project team meetings
Seniority
Senior, hands-on IC