Location
- Poland
- Spain
- United Kingdom
- South Africa
The role
You'll lead the development of high-quality regulatory and clinical documents, overseeing medical writing workstreams and ensuring deliverables meet quality and timeline expectations. You'll collaborate with clinical research, biostatistics, and regulatory affairs teams, mentor junior writers, and act as lead medical writer on complex projects including major international regulatory submissions. This is a remote full-time position with the company, contingent on your legal right to work in your country of residence.
At a glance
- Education
- Bachelor's Degree
- Experience
- 5+ years
- Level
- Senior
- Work authorization
- Required
Tools and skills
Skills
Content CreationScientific WritingClinical DocumentationMedical WritingRegulatory RequirementsRegulatory SubmissionsInvestigator BrochuresClinical Study ReportsTrainingMentoringLeadershipCommunicationCollaborationAttention to DetailManaging multiple prioritiesEditing