Senior Medical Writer - Early Development Services
PPD (Thermo Fisher)
UK
Not specified; not specified; competitive salary +...
5+ years regulatory writing experience
Bachelor's degree in scientific discipline
Experience managing complex medical writing projects
The role involves serving as a primary author for routine documents such as clinical study reports and study protocols while assisting with complex program-level documents
Job Summary
The role involves serving as a primary author for routine documents such as clinical study reports and study protocols while assisting with complex program-level documents.
Candidates must ensure compliance with quality processes and possess extensive knowledge of regulatory guidelines and drug development processes.
PPD offers an award-winning learning and development programme along with a flexible working culture that values work-life balance.
Matching Summary
The role involves serving as a primary author for routine documents such as clinical study reports and study protocols while assisting with complex program-level documents.
Salary
Not specified; Not specified; Competitive salary and extensive benefits package
Skills & Requirements
Must-have
5+ years regulatory writing experience
Bachelor's degree in scientific discipline
Experience managing complex medical writing projects