As a Safety Writer III, you will be responsible for the planning, coordination, and delivery of safety writing services for clinical trial and/or marketed product projects
Job Summary
As a Safety Writer III, you will be responsible for the planning, coordination, and delivery of safety writing services for clinical trial and/or marketed product projects.
You will perform day-to-day safety writing and related activities within a highly regulated pharmacovigilance environment, driven by strict timelines.
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence.
Matching Summary
As a Safety Writer III, you will be responsible for the planning, coordination, and delivery of safety writing services for clinical trial and/or marketed product projects.
Skills & Requirements
Must-have
Safety writing deliverables
Pharmacovigilance environment
ICH and US aggregate safety reporting
Project management
Data review and authoring
Quality and senior review
Nice-to-have
Scientific safety services support
Lead role and mentorship
Positive and professional demeanor
Team collaboration
Key Requirements
Bachelor's or higher scientific degree
Minimum 6 years experience
Authoring and quality control review of DSURs, PBRERs/PSURs, PA(D)ERs, RMPs