Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer
Job Summary
Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.
Conducts data review, authoring, quality review, and project manages a wide range of clinical trial and marketed product safety writing deliverables.
As the trusted partner of some of the most innovative big pharma and biotech companies; our Safety Writers have the opportunity to work on challenging projects across a wide range of therapeutic areas.
Matching Summary
Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.
Skills & Requirements
Must-have
Authoring clinical trial safety deliverables
Project management of safety writing
Client interaction and communication
Regulatory authority assessment report responses
Aggregate safety report writing guidelines
Nice-to-have
Scientific safety services support
Subject matter expert in designated area
Mentoring less experienced staff
Key Requirements
Bachelor’s or higher scientific degree
Minimum 2 years experience authoring DSURs, PBRERs/PSURs, PA(D)ERs, or RMPs