You will play a pivotal role in ensuring that all documents authored by the Safety Surveillance and Aggregate reports (SSA) team adhere to the highest quality standards set by Biogen
Job Summary
You will play a pivotal role in ensuring that all documents authored by the Safety Surveillance and Aggregate reports (SSA) team adhere to the highest quality standards set by Biogen.
This position involves a critical eye for detail, where you will verify data accuracy, ensure stylistic consistency, and maintain compliance with Biogen's style guide.
By collaborating with internal and external stakeholders, you will uphold the quality of our pharmacovigilance efforts and drive improvements in our quality documentation processes.
Matching Summary
You will play a pivotal role in ensuring that all documents authored by the Safety Surveillance and Aggregate reports (SSA) team adhere to the highest quality standards set by Biogen.
Skills & Requirements
Must-have
Source data verification
Editorial and scientific reviews
Pharmacovigilance experience
Medical terminology
Biogen style guide compliance
Nice-to-have
Process improvement initiatives
Collaborative environment
Pioneering spirit
Commitment to excellence
Key Requirements
Bachelor’s Degree in biologic or natural science, or healthcare discipline
Previous experience in pharmacovigilance, medical writing, scientific editing and/or publishing
Significant years of writing and editing experience
Familiarity with pharmacovigilance and drug development
In depth knowledge of common data processing software